Boston Scientific Corporation recalls
169 recalls in our records from 2012 to 2026: 169 FDA medical devices.
Recalls with full detail pages
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Boston Scientific Corporation medical device recall: Imager II Angiographic Catheters M001314001 IMAGER II/5/ST/65/038 BX5
Tip may fracture or detach, leading to device fragments remaining within the patient or migrating through the vasculature. Patient impact may include prolonged procedure…
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Boston Scientific Corporation medical device recall: Boston Scientific ENROUTE Transcarotid Neuroprotection System
Potential for arterial sheath tip separation or partial tip separation during use.
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Boston Scientific Corporation medical device recall: Boston Scientific Pacemaker
Updated software, Brady software maintenance release 6 (SMR6), is now available for the ACCOLADE" family of pacemakers and cardiac resynchronization therapy pacemakers…
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Boston Scientific Corporation medical device recall: AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm
Increased reports of stent deployment and expansion issues. The most common outcome reasonably foreseeable resulting from difficulty deploying the stent is prolongation…
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Boston Scientific Corporation medical device recall: Accolade Sr Sl
Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for…
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Boston Scientific Corporation medical device recall: WATCHMAN TruSeal Access System SGL
Boston Scientific has identified a higher likelihood of air embolism events when procedures are performed without positive pressure-controlled ventilation. According to…
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Boston Scientific Corporation medical device recall: Endotak Reliance G/Sg
Affected lead models may experience gradually rising LVSI measurements in association with calcification of the defibrillation lead coils. The issue may lead to early…
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Boston Scientific Corporation medical device recall: Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding…
Certain batches are being removed due to an increase in complaints received in which physicians encountered greater than anticipated resistance while attempting to…
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Boston Scientific Corporation medical device recall: ACCOLADE DR Pacemaker
A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built before September 2018, have an increased potential to initiate Safety Mode during telemetry…
Earlier and other recalls
These link to the official agency notice.
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Boston Scientific Corporation medical device recall: NaviFlex LW Pusher Official notice ↗
Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device…
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Boston Scientific Corporation medical device recall: Boston Scientific Corporation StoneSmart Connect Console Contents Official notice ↗
A subset of power adapters used with the connect console may exhibit higher-than-expected resistance in the electrical grounding path. As a result, the power adaptor may…
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Boston Scientific Corporation medical device recall: LUX-Dx Official notice ↗
There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification…
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Boston Scientific Corporation medical device recall: OverStitch Suture Cinch Official notice ↗
Device may fail to deploy the cinch implant and/or fail to cut the suture as intended.
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Boston Scientific Corporation medical device recall: Radial Jaw 4 Standard Capacity Biopsy Forceps with the following… Official notice ↗
Potential for breach in sterile barrier of device packaging.
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Boston Scientific Corporation medical device recall: FARADRIVE Steerable Sheath Clear IDE Official notice ↗
Boston Scientific's complaint investigations have identified that a subset of air ingress complaints are associated with hemostatic valve damage related to dilator…
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Boston Scientific Corporation medical device recall: FARASTAR Ablation Generator EU Official notice ↗
Boston Scientific is replacing specific FARASTAR PFA generators which have a configuration that is not compatible for use with the FARAPOINT PFA catheter.
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Boston Scientific Corporation medical device recall: Boston Scientific TheraSphere 360 Y-90 Management Platform Official notice ↗
Software anomaly occurs when a user adds one or more vials to the cart and subsequently returns to the Activity Calculator to modify one or more input. When a user…
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Boston Scientific Corporation medical device recall: FARASTAR Ablation Generator EU Official notice ↗
Labeling discrepancy: Devices distributed with Instructions For Use (IFU) did not include FARAPOINT PFA catheter information.
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Boston Scientific Corporation medical device recall: Rapid Refill Continuous Injection System Official notice ↗
Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the manifold,…
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Boston Scientific Corporation medical device recall: CRE Pro Wireguided 6-8mm 240cm Official notice ↗
Potential sterile breach of the pouches in which devices are packaged.
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Boston Scientific Corporation medical device recall: Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump Official notice ↗
There is the potential for leakage along the drug pathway from the pump through the end of the catheter.
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Boston Scientific Corporation medical device recall: Orca Single Use Air/Water and Suction Valves Official notice ↗
Boston Scientific is initiating a medical device removal of Orca Sterile, Single Use Air/Water and Suction Valves due to a higher than anticipated occurrence of the…
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Boston Scientific Corporation medical device recall: Lux-Dx Ii Official notice ↗
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for…
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Boston Scientific Corporation medical device recall: EndoVive Safety PEG Kit Official notice ↗
Recall of kits which utilized ChloraPrep Triple Swabsticks from BD. Open or compromised seals on the sterile swabstick packaging, which could result in loss of sterility…
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Boston Scientific Corporation medical device recall: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter Official notice ↗
Boston Scientific is initiating the removal of certain batches of Coyote" Over-the-Wire (OTW) Percutaneous Transluminal Angioplasty (PTA) Balloon Dilatation Catheter…
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Boston Scientific Corporation medical device recall: TENACIO Pump with InhibiZone Official notice ↗
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
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Boston Scientific Corporation medical device recall: Extractor Pro RX Retrieval Balloon Catheter Official notice ↗
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
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Boston Scientific Corporation medical device recall: ICEfx Cryoablation System Official notice ↗
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
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Boston Scientific Corporation medical device recall: Boston Scientific Encore 26 Inflation Device Official notice ↗
The Encore 26 Inflation Device is used with balloon dilation catheters to create and monitor pressure in the balloon and to deflate the balloon. An internal…
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Boston Scientific Corporation medical device recall: FARAWAVE 1.0 Pulsed Field Ablation Catheter Official notice ↗
The potentially impacted units were manufactured using specific equipment that may have caused cracks in the electrode bands on the catheter's distal end.
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Boston Scientific Corporation medical device recall: VersaCross Access Solution Official notice ↗
Potential for hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. Issue could potentially lead to systemic infection and sepsis…
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Boston Scientific Corporation medical device recall: IceSeed 1.5 CX S NEEDLE US Official notice ↗
Boston Scientific has identified that IceSeedTM CX needles manufactured between April 2024 and February 2025 have been programmed with DEMO settings instead of…
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Boston Scientific Corporation medical device recall: AXIOS Stent and Electrocautery- Enhanced Delivery System 10mmx10mm… Official notice ↗
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the…
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Boston Scientific Corporation medical device recall: AMS Artificial Urinary Sphincter Control Pump Official notice ↗
Potential for mislabeled packaging in which a device labeled as a Pressure Regulating Balloon (UPN 72400024) which instead contained a Control Pump (UPN 72400098)
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Boston Scientific Corporation medical device recall: Boston Scientific POLARx BALLOON CATHETER ST 28MM OUS Official notice ↗
Boston Scientific is updating the instructions for use of their POLARx and POLARx FIT Cryoablation Balloon Catheters related to Atrio-esophageal Fistula Risk.
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Boston Scientific Corporation medical device recall: Boston Scientific myLUX Patient Application for an Apple Mobile device Official notice ↗
Patients using the Model 2939 myLUX Patient Application on their Apple mobile device (e.g., iPhone) may not be transmitting data from their Insertable Cardiac Monitor to…
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Boston Scientific Corporation medical device recall: Boston Scientific AVVIGO+ Multi-Modality Guidance System Official notice ↗
Boston Scientific has received reports indicating the grid mark overlay on the cross-sectional view did not present correctly when an OptiCross 18 Peripheral Imaging…
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Boston Scientific Corporation medical device recall: WALLFLEX FC ESO STENT RMV 18X103MM- Wallflex Esophageal Partially… Official notice ↗
WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.
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Boston Scientific Corporation medical device recall: Flexima APDL Drainage Catheter System and Kit Official notice ↗
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
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Boston Scientific Corporation medical device recall: Capio SLIM Suture Capturing Device Official notice ↗
Some lots of Capio SLIM do not consistently catch the suture after activation possibly resulting in a prolonged procedure or additional medical intervention.
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Boston Scientific Corporation medical device recall: Autotome RX 20mm CUT WIRE Cannulating Sphincterotome Official notice ↗
Foreign material may be present on the enclosed section of the cutting wire which may lead to inability to optimally bow the sphincterotome. This issue may lead to…
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Boston Scientific Corporation medical device recall: Expo 5F Selective Angiographic Catheters Official notice ↗
An increase in complaints related to an inability to advance the guidewire through the lumen of the device for certain batches. There is evidence of the polyurethane…
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Boston Scientific Corporation medical device recall: EndoVive 20Fr Push Safety PEG Kit w/ENFit Official notice ↗
Inability to advance the guidewire through the feeding tube during placement due to blocked lumen of the barb connector. May lead prolongation in the procedure to…
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Boston Scientific Corporation medical device recall: OptiCross Coronary Imaging Catheter Official notice ↗
Certain batches of Opticross 40MHz Coronary Imaging Catheters manufactured using an incorrect voltage setting, which may have resulted in decreased image brightness.
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Boston Scientific Corporation medical device recall: Obsidio Conformable Embolic Official notice ↗
An investigation determined that delivery of the Obsidio embolic using the aliquot technique for lower gastrointestinal bleeding embolization poses a high risk of bowel…
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Boston Scientific Corporation medical device recall: Boston Scientific POLARSHEATH Steerable Sheath 12F Official notice ↗
Boston Scientific has identified a tooling error in manufacturing which may have caused delamination of the inner lumen of the sheath shaft in a subset of POLARSHEATH…
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Boston Scientific Corporation medical device recall: Boston Scientific iSLEEVE EXPANDABLE Introducer Set REF H74939349140 Official notice ↗
Boston Scientific is conducting a removal of specific batches of the iSLEEVETM 14F Expandable Introducer Set due to complaints associated with a hemostatic valve leak.
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Boston Scientific Corporation medical device recall: EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM Official notice ↗
Affected batches of the kit contain Stoma Measuring Devices sized to measure for an 18/24F replacement button, but are labeled as being for a 28F. Use of defective…
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Boston Scientific Corporation medical device recall: Boston Scientific Model 3120 ZOOM LATITUDE Programmer/Recorder/Monitor Official notice ↗
The software application on the Programmer/Recorder/Monitor (PRM) for Implantable Pulse Generators will display certain diagnostic dates incorrectly, with a year in the…
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Boston Scientific Corporation medical device recall: EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 &… Official notice ↗
Poor image quality due to fluid ingress in the lens.
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Boston Scientific Corporation medical device recall: Guider Softip Guide Catheter 6F PRE-SHAPED 40 90CM Official notice ↗
Stryker Neurovascular has observed that certain lots of Guider Softip XF Guide Catheters appear to have the incorrect tip curve shape. The impacted products were…
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Boston Scientific Corporation medical device recall: EMBLEM S-ICD Pulse Generator Model A209 Official notice ↗
There is a potential for a rare interaction between the EMBLEM S-ICD and LATITUDE communicator, which may cause S-ICD sensing disablement for a 24-hour interval.
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Boston Scientific Corporation medical device recall: Flexiva Pulse 242 Single-Use Laser Fibers-intended to be used as a… Official notice ↗
Manufactured with the incorrect component may result in lower power output and degradation or dimming of the aiming beam, leading to reduced efficiency of fiber…
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Boston Scientific Corporation medical device recall: WATCHDOG Hemostasis Valve Kit Official notice ↗
The firm received complaints of the Insertion Tool component being occluded, resulting in the inability to pass a guidewire through the tool.
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Boston Scientific Corporation medical device recall: Habib EndoHPB Bipolar Radiofrequency Official notice ↗
Cease use of the Habib EndoHPB Bipolar RF Catheter with the ERBE VIO3 Generator immediately due to the potential for delivery of excessive energy leading to thermal…
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Boston Scientific Corporation medical device recall: LATITUDE NXT Remote Patient Management System Official notice ↗
Under specific circumstances, the U.S. product registration system did not send up enablement requests to U.S. LATITUDE Customer Support during an 8-month interval in…
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Boston Scientific Corporation medical device recall: ORISE Gel Submucosal Lifting Agent--Indicated for use in… Official notice ↗
***Update12/13/22***:Product removal due to higher incidence of adverse events of foreign body reactions*** Potential outcomes associated with foreign body reaction to…
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Boston Scientific Corporation medical device recall: Emblem S-Icd Official notice ↗
There is an incorrect manufacturing date/timestamp within the software which causes an inaccurate display of battery capacity.
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Boston Scientific Corporation medical device recall: EKOS Control Unit 4.0 console Official notice ↗
Consoles were shipped without an instruction for use (IFU) or with the incorrect IFU.
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Boston Scientific Corporation medical device recall: The Programmer/Recorder/Monitor Official notice ↗
There is potential for unanticipated software anomalies to occur when using the Model 2868 Application loaded on the 3120 ZOOM LATITUTDE programmer when communicating…
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Boston Scientific Corporation medical device recall: Boston Scientific Guider Softip XF Official notice ↗
The impacted products were distributed with an MPXF tip curve shape instead of the 40XF tip curve shape for the Guider/40XF/8FR/90CM guide catheter.
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Boston Scientific Corporation medical device recall: EkoSonic Kit 135cm Official notice ↗
Product may be mislabeled.
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Boston Scientific Corporation medical device recall: GreenLight HPSEA Laser Fibers Official notice ↗
Several complaints were received for the affected lot; users received a "Fiber type does not match card type" error message on the GreenLight XPS Laser console,…
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Boston Scientific Corporation medical device recall: EXALT Model D Single- Use Duodenoscope Official notice ↗
Updated Instructions for Use (IFU) for EXALT Model D Single-Use Duodenoscope highlight the known risk of perforation and provide best clinical practices related to…
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Boston Scientific Corporation medical device recall: SpaceOAR System Official notice ↗
Users need to be aware that embolism is a possible adverse event associated with hydrogel misplacements. Updated IFU provides new procedural instructions, warnings and…
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Boston Scientific Corporation medical device recall: ROTAWIRE Drive and wireClip Torquer Official notice ↗
Pouch seals may be open, compromising sterility.
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Boston Scientific Corporation medical device recall: Dreamtome RX Cannulating Sphincterotome-DREAMTOME 44-20MM/260CM… Official notice ↗
Sterility of device is compromised due to a sterile barrier breach
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Boston Scientific Corporation medical device recall: Boston Scientific ROTAPRO Official notice ↗
Manufacturing instructions did not include the directions to not retest the pneumatic kit component of the ROTAPRO console upon failure, an internal nonconformity.
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Boston Scientific Corporation medical device recall: HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of… Official notice ↗
Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure
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Boston Scientific Corporation medical device recall: TheraSphere Administration Set Official notice ↗
Potential for leaks and loosening at the patient catheter connection
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Boston Scientific Corporation medical device recall: Advantio Dr El Official notice ↗
The dual chamber INGENIO family pacemakers or cardiac resynchronization therapy pacemakers (CRT-Ps) may initiate Safety Mode later in device life (i.e., prior to…
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Boston Scientific Corporation medical device recall: Essentio pacemaker Official notice ↗
Latent release of small amounts of hydrogen within the pacemaker may cause a low voltage capacitor to become electrically compromised over time resulting in accelerated…
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Boston Scientific Corporation medical device recall: ELUVIA Drug-Eluting Vascular Stent System - Product Usage: indicated… Official notice ↗
One batch of the ELUVIATM Drug Eluting Vascular Stent System incorrect placement of some 6x40mm ELUVIA stents into 6x100mm packaging.
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Boston Scientific Corporation medical device recall: VICI VENOUS STENT System Product Usage: is intended for the treatment… Official notice ↗
The firm has received reports of stent migration after implantation
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Boston Scientific Corporation medical device recall: Colpassist Vaginal Positioning Device - Product Usage: intended for… Official notice ↗
Potential for pinholes (sterile barrier breach) on the edge of the pouch to potentially render the device non-sterile, and may result in a post-operative infection
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Boston Scientific Corporation medical device recall: EXALT Controller - Product Usage: intended for use with a Boston… Official notice ↗
May have been programmed with a less than optimal brightness setting resulting in a darker than desired image
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Boston Scientific Corporation medical device recall: The AMS 700 Inflatable Penile Prosthesis is a closed fluid-filled… Official notice ↗
An AMS 700 100 mL Spherical Reservoir with InhibiZone was incorrectly labeled as a 100 mL Conceal Reservoir with InhibiZone.
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Boston Scientific Corporation medical device recall: MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over… Official notice ↗
The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex 135 Microcatheters due to incorrect labeling and packaging.
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Boston Scientific Corporation medical device recall: Captivator Single-Use Polypectomy Snares Official notice ↗
Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.
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Boston Scientific Corporation medical device recall: EMBLEM S-ICD Model A209 Official notice ↗
Electrical overstress may lead to device malfunction.
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Boston Scientific Corporation medical device recall: EMBLEM S-ICD pulse generators Official notice ↗
Accelerated battery depletion may result in a need for device replacement earlier than expected.
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Boston Scientific Corporation medical device recall: ACUITY Universal Cutter Official notice ↗
Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters distributed in the US that did not undergo the applicable sterile processing procedure.
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Boston Scientific Corporation medical device recall: EMBLEM S-ICD Subcutaneous Electrode Model 3501. Component of… Official notice ↗
There is potential for fractures which results in the inability to delivery therapy.
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Boston Scientific Corporation medical device recall: Lotus Edge Valve System Official notice ↗
Failure to execute the visual inspection correctly prior to locking the valve during the deployment process can lead to the inability to release the delivery system.
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Boston Scientific Corporation medical device recall: AXIOS Stent and Electrocautery - Enhanced Delivery System 10mm x10mm… Official notice ↗
The rotating luer fitting at the distal end of the delivery system handle may become detached from the nose of the delivery during device preparation, stent delivery or…
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Boston Scientific Corporation medical device recall: Contour VL Variable Length Ureteral Stent Official notice ↗
Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.
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Boston Scientific Corporation medical device recall: IceFORCE" 2.1 CX 90¿ Cryoablation Needle Official notice ↗
Complaint trend regarding needle shaft gas leaks.
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Boston Scientific Corporation medical device recall: EKOS Control System Official notice ↗
This is a follow-up to the EKOS Field Safety Notice dated April 30, 2019. The Radio Frequency (RF) board has been redesigned to prevent occasional internal board…
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Boston Scientific Corporation medical device recall: AMS 700 MS Pump with and without InhibiZone Official notice ↗
The recalling firm has observed an increase in complaints of problems encountered during the initial activation of the device in which the patient and/or the physician…
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Boston Scientific Corporation medical device recall: Model 3300 LATITUDE Programming System with installed Model 3892… Official notice ↗
There is potential when a user changes an EGM trace channel with a Manual Pace Threshold test in progress that the newly modified trace channel may change to a flat line.
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Boston Scientific Corporation medical device recall: Visual-ICE MRI Cryoablation System Mobile Connection Panel Official notice ↗
Incorrectly installed base.
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Boston Scientific Corporation medical device recall: Hurricane RX Biliary Balloon Dilatation Catheter Catalog REF No.… Official notice ↗
RX tunnel component (black sheath) may detach from the catheter shaft due to lower bond strength.
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Boston Scientific Corporation medical device recall: Opticross 35 15 MHz Peripheral Imaging Catheter 8F Official notice ↗
Opticross 35 Peripheral Imaging Catheter is being recalled because the incremental telescoping length markings near the proximal end of the catheter shaft can flake off…
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Boston Scientific Corporation medical device recall: WallFlexTM Biliary RX Fully Covered Stent System RMV Official notice ↗
Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices labeled as WallFlexTM Biliary RX Fully Covered Stent System RMV 10x60mm device
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Boston Scientific Corporation medical device recall: Captivator Polypectomy Snare Official notice ↗
BSC has noted a potential inability to cut and remove polyps for these lots/batches. potential consequences related to the snares not performing as intended would be a…
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Boston Scientific Corporation medical device recall: Ablation Galil Technology Official notice ↗
The needle surface deteriorated due to unexpected electrolysis during procedure.
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Boston Scientific Corporation medical device recall: AMS 700 100 mL Official notice ↗
A labeling discrepancy incorrectly labeled AMS 700 100mL Conceal Low Profile Reservoir with InhibiZone as 100mL Spherical Reservoir with InhibiZone.
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Boston Scientific Corporation medical device recall: MoXy Laser Fiber Official notice ↗
To reinforce existing instructions within the Directions for Use (DFU) and provide further guidance which will be added to the DFU that may reduce the likelihood of…
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Boston Scientific Corporation medical device recall: iLab Polaris Multi-Modality Guidance System Official notice ↗
Certain iLab Polaris Systems which were upgraded with a previous 2.10 software version (disk batch 629774) contained a bug in which only the True Color Secondary Capture…
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Boston Scientific medical device recall: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX STR/150CM UPN:… Official notice ↗
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected…
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Boston Scientific Corporation medical device recall: Imager II 5F Angiographic Catheters Official notice ↗
Potential for tip detachment of Imager II 5F Angiographic Catheters
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Boston Scientific Corporation medical device recall: Boston Scientific Official notice ↗
Boston Scientific released a new Software Update Application that was downloaded to four (4) distributed Model 3300 programmers. The Software Update Application then…
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Boston Scientific Corporation medical device recall: AngioJet Ultra Consoles-Thrombectomy System UPN: 105650-001D… Official notice ↗
Missing Directions for Use (DFU) - Consoles shipped to customers without the required Operator's Manual.
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Boston Scientific Corporation medical device recall: Habib EUS RFA Official notice ↗
During testing on the Habib EUS RFA device, a temperature increase was observed at the tip of the EUS-FNA needle. It was determined that capacitive 5 coupling presents a…
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Boston Scientific Corporation medical device recall: Emerge Monorail PTCA Dilatation Catheter. Sterilized using ethylene… Official notice ↗
Certain dilation and extension catheters are being recalled because these catheters may have missed the hydrophilic coating step, which creates a lubricious surface on…
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Boston Scientific Corporation medical device recall: Boston Scientific Advanix Pancreatic Stent Official notice ↗
Product manufactured between September 29, 2017 and September 12, 2019 have been labeled with a 36-month shelf life rather than the approved 18-month shelf life
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Boston Scientific Corporation medical device recall: Subcutaneous Implantable Cardioverter Defibrillator Official notice ↗
Potential need for device replacement - Elective Replacement Indicator (ERI) or End of Life (EOL) - earlier than expected due to compromised performance of an electrical…
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Boston Scientific Corporation medical device recall: AMS 800 Artificial Urinary Sphincter AMS 800 Belt Cuff Official notice ↗
Mislabled: AMS 800 occlusive cuff labeled as 4.5 cm was a length of 4.0 cm and therefore..
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Boston Scientific Corporation medical device recall: AURIGA XL 4007 BRAZIL SYSTEM Model: M0068FS4007B0 Product Usage: The… Official notice ↗
Certain Auriga consoles may exhibit faster than normal power degradation due to a potential issue in the mechanical cooling system that could lead to a low power error…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.