Becton Dickinson & Company recalls
162 recalls in our records from 2012 to 2026: 161 FDA medical devices, 1 FDA drugs.
Recalls with full detail pages
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Becton Dickinson & Company medical device recall: BD¿Spinal Tray with BD¿Quincke Needle 22 G x 3.5 in
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality…
Earlier and other recalls
These link to the official agency notice.
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Becton Dickinson & Co. medical device recall: BD Phoenix Panel NMIC-312. Catalog Number: 449082 Official notice ↗
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.
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Becton Dickinson & Co. medical device recall: BD GasPak EZ CO2 Pouch System. Catalog Number: 260684. for… Official notice ↗
BD identified an issue affecting certain lots of BD GasPak EZ CO2 and BD GasPak EZ Campy Gas Generating Pouch Systems, where gas generating sachets may produce carbon…
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Becton Dickinson & Company medical device recall: 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number:… Official notice ↗
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
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Becton Dickinson & Company medical device recall: BD Luer Tip Caps Official notice ↗
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
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Becton Dickinson & Co. medical device recall: BD Kiestra" Isolate Suspension Cuvette Array Official notice ↗
The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument…
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Becton Dickinson & Co. medical device recall: BD EpiCenter Microbiology Data Management System Official notice ↗
Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service…
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Becton Dickinson & Co. medical device recall: BD COR System Software. Model Number: 444829 Official notice ↗
Potential for functionality issue that supports the Over labeling feature and could lead to possible false negative results.
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Becton Dickinson & Co. medical device recall: BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for… Official notice ↗
BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.
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Becton Dickinson & Co. medical device recall: BD BBL TB Stain Kit K Official notice ↗
One component of the kit was shipped with an expiration date of 30Sep2024 while the Certificate of Analysis (COA) indicated an expiration date of 30Apr2025.
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Becton Dickinson & Co. medical device recall: BD PCR Cartridges used with MAX System. Model Number: 437519 Official notice ↗
Potential for signal drift in specific lots of BD PCR Cartridges.
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Becton Dickinson & Co. medical device recall: BD BBL Sensi Disc Ampicillin 2 ¿g Official notice ↗
BD identified through potency testing as part of a stability test request to monitor Ampicillin AM-2 due to decrease in potency results of 65% at 18 months, may result…
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Becton Dickinson & Co. medical device recall: BD EpiCenter Single User Software Version or Model: 441007 Catalog… Official notice ↗
BD confirmed that product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these…
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Becton Dickinson & Co. medical device recall: BD Synapsys Informatics Solution with software versions: 4.20 Official notice ↗
Synapsys software versions 4.20, 4.30, 5.10, 5.20, or 5.30 and utilizing the in-line breakpoint feature, an error is occurring where BD Synapsys will incorrectly display…
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Becton Dickinson & Co. medical device recall: BD Phoenix M50 instrument -Intended for the rapid identification Official notice ↗
Escherichia coli (E. coli) misidentification for clinical samples that were tested on BD Phoenix" M50 instrument and BD Phoenix" 100, may lead to misdiagnosis and…
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Becton Dickinson & Co. medical device recall: BD BACTEC MGIT 960 PZA Kit)- IVD qualitative procedure for… Official notice ↗
May intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of Mycobacterium tuberculosis isolates.
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Becton Dickinson & Co. medical device recall: BD Kiestra Urine Culture Application Powered by BD Synapsys… Official notice ↗
There is a potential risk that the image colony count does not adequately reflect the actual plate colony count and may lead to inaccurate counts that would impact…
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Becton Dickinson & Co. medical device recall: BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to detect… Official notice ↗
Assays may produce false negative results due to decreased activity of the enzyme utilized in manufacturing.
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Becton Dickinson & Co. medical device recall: BD Phoenix NMIC-306 Panel is a self-inoculating Official notice ↗
Products were found to have confirmed drug cross contamination prior to release may lead to incorrect, inadequate, or absent antibiotic treatment or delay in results
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Becton Dickinson & Co. medical device recall: Sensi Disc Amoxicillin with Clavulanic Acid 20/10 ¿g Official notice ↗
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard,…
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Becton Dickinson & Company medical device recall: PosiFlush Prefilled Saline Syringe with General Pump Compatibility Official notice ↗
An incorrect stopper was used in nine lots of 10mL BD PosiFlush Normal Saline Flush Syringes with General Pump Compatibility. The use of BD PosiFlush Prefilled Flush…
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Becton Dickinson & Company medical device recall: BD Alaris Pump infusion sets Official notice ↗
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).
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Becton Dickinson & Co. medical device recall: BD BACTEC Plus Aerobic/F Culture Vials Official notice ↗
Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.
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Becton Dickinson & Co. medical device recall: BD Synapsys Informatics Solution Official notice ↗
There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near…
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Becton Dickinson & Co. medical device recall: BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B Official notice ↗
IFU- Instructions for Use (IFU) package insert and both the IFU packaged with the test kit and the electronic version on the BD website not approved by FDA,specifically…
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Becton Dickinson & Co. medical device recall: BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software… Official notice ↗
Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as part of the Icefall A platform, plate information was not visible in Synapsys" after…
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Becton Dickinson & Company medical device recall: BD Ultra-Fine Insulin Syringe 0.5mL Official notice ↗
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
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Becton Dickinson & Co. medical device recall: BBL Chocolate II Agar- IVD for the isolation and cultivation of… Official notice ↗
Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide and does not provide enough of the blood factors necessary to support Haemophilus growth. The…
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Becton Dickinson & Co. medical device recall: BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the… Official notice ↗
Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against…
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Becton Dickinson & Company medical device recall: BD Vacutainer Tube Sodium Fluoride: 100 mg Official notice ↗
The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The…
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Becton Dickinson & Company medical device recall: BD PhaSealTM Y-Site Connector Official notice ↗
Incorrect expiration date listed on the product labels. The expiration date listed on the product label is beyond the expiration date of the product.
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Becton Dickinson & Company medical device recall: BD Connecta Stopcock with OFF Directed Tap Without Extension Tube Official notice ↗
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous…
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Becton Dickinson & Co. medical device recall: BD Synapsys Microbiology Informatics Solution Official notice ↗
When updating BD Kiestra customers to BD Synapsys version 4.10, the custom antibiotic codes set by the customer are overwritten with the BD default antibiotic codes.
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Becton Dickinson & Company medical device recall: BD Vacutainer Luer Lok Access Device - intended as a sterile Official notice ↗
May shed contaminant particles into the urine specimen that may be misidentified as Red Blood Cells when used in conjunction with the Sysmex UF-1000i or UX-2000…
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Becton Dickinson & Co. medical device recall: BD Veritor Plus Analyzer - intended to provide rapid test results in… Official notice ↗
May have the potential to overheat and/or cause fire, the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to…
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Becton Dickinson & Company medical device recall: BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf… Official notice ↗
Holes in product packaging impacts package integrity and may compromise sterility.
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Becton Dickinson & Co. medical device recall: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for… Official notice ↗
BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were not adequately sealed causing some tubes to be partially filled or empty upon use. A partially…
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Becton Dickinson & Co. medical device recall: BD BBL Martin-Lewis Agar Official notice ↗
Products show heavy growth of C. albicans after 24 hours of incubation due to misformulation (expected reaction is partial inhibition after 18-48 hours incubation) and…
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Becton Dickinson & Company medical device recall: BD Hypodermic Syringe 10 ml Official notice ↗
The product packaging for the 10 ml eccentric tip syringe may exhibit open seals. An open seal impacts package integrity and potentially compromises sterility of the…
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Becton Dickinson & Co. medical device recall: BioGX SARS-CoV-2 Reagents for BD MAX System Catalog number Official notice ↗
Some N1 and N2 master mix pouches packaged within the lots of BioGX SARS-CoV-2 Reagents for BD MAX System may be mislabeled. This could result in a kit containing two…
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Becton Dickinson & Company medical device recall: BD Stimex Insulated Needle 22G x 2.13in Official notice ↗
BD was advised by the European Notified Body, NSAI, that the instructions for use (IFU) needs to be updated to include the general contraindications
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Becton Dickinson & Co. medical device recall: BD Phoenix PMIC/ID-105: IVD is intended for the in vitro rapid… Official notice ↗
BD Phoenix Sulfamethoxazole-trimethoprim (SXT) Resistance, false resistant SXT result with S. aureus could lead to a potential loss of access to a preferred antibiotic…
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Becton Dickinson & Company medical device recall: BD PrecisionGlide Needle 30G x 1/2 Official notice ↗
BD has confirmed the presence of blood on the cannulas of the BD PrecisionGlide needles 30G X 1/2" Lot No. 9128897. The possibility of infection may be present if the…
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Becton Dickinson & Company medical device recall: BD Ultra-Fine Pen Needles 32G x 4mm Official notice ↗
Product shelf cartons incorrectly labeled as products intended for the Latin American market. Although the product description on the label 32G x 4mm pen needles is…
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Becton Dickinson & Company medical device recall: Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access… Official notice ↗
Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.
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Becton Dickinson & Company medical device recall: BD Nexiva Closed IV Catheter System Dual Port Official notice ↗
Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis or treatment until a new needle is inserted
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Becton Dickinson & Company medical device recall: BD SafetyGlideTM 3ml 25G x 1 3mL SafetyGlide syringes Official notice ↗
Printed scale markings on the 3mL SafetyGlide syringes, with catalog # 305924, Lot# 8289599, are printed incorrectly. The scale is skewed to different degrees, resulting…
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Becton Dickinson & Co. medical device recall: BD MAX SARS-CoV-2 Reagents Official notice ↗
BD is experiencing elevated rates of potential false positive results from certain customers when using the BD SARS-CoV-2 Reagents for the BD MAX System. False positive…
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Becton Dickinson & Company medical device recall: PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access… Official notice ↗
Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting…
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Becton Dickinson & Co. medical device recall: BD BBLTM Gram Crystal Violet 250mL-- IVD Primary stain for Staining… Official notice ↗
May exhibit increased levels of artifacts which could be difficult to distinguish from gram positive cocci, increased levels of artifacts could result in a…
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Becton Dickinson & Company medical device recall: BD Posiflush SF Saline Flush Syringe Official notice ↗
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
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Becton Dickinson & Company medical device recall: BARD MYPICC KIT 5F Dual-Lumen Official notice ↗
The kits contain surgical gowns which were subject to a recall by the supplier.
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Becton Dickinson & Company medical device recall: PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge Official notice ↗
Iincorrectly packaged without the required lidocaine as labeled
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Becton Dickinson & Company medical device recall: CareFusion Safe-T-Centesis Catheter Drainage Tray Official notice ↗
The 8 Fr catheter was manufactured with the 6.9 Fr needle instead of the 8 Fr needle.
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Becton Dickinson & Company medical device recall: Site~Rite 8 Ultrasound Systems-intended for diagnostic ultrasound… Official notice ↗
The indicator may show available charge when the battery is close to depletion. As a result, the Site~Rite 8 has the potential to abruptly shut down, without advance…
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Becton Dickinson & Company medical device recall: BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547 Official notice ↗
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
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Becton Dickinson & Company medical device recall: 13 Fr. Trialysis Catheter with Alphacurve. Catalog No. 5653150. UDI:… Official notice ↗
A portion of the lot was incorrectly packaged with a 12.5cm catheter instead of a 15cm catheter.
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Becton Dickinson & Company medical device recall: MaxZero Extension Sets with Needle-less Connector Official notice ↗
BD has decided to initiate a voluntary recall due to a confirmed complaint trend for droplets of fluid separating from the sealed surface of the MaxZero connector,…
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Becton Dickinson & Company medical device recall: BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25 Official notice ↗
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
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Becton Dickinson & Company medical device recall: BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached… Official notice ↗
Separation of front and rear barrels upon activation of the safety feature that retracts the needle
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Becton Dickinson & Company medical device recall: CareFusion MaxPlus Clear Needleless Connector. Intended for Positive… Official notice ↗
After disconnection of a luer, the valve of the connector remains recessed; not fully closing, either temporarily or permanently. The risks of blood loss and air…
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Becton Dickinson & Company medical device recall: BD Microtainer Z Official notice ↗
Damaged reservoir may lead to a decreased fill volume causing samples to be insufficient for testing and improper blood-to-additive ratio, potentially producing…
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Becton Dickinson & Co. medical device recall: BD Kiestra InoqulA Software Version 20.3.IVD automated specimen… Official notice ↗
An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate
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Becton Dickinson & Company medical device recall: 8 G x 10 CM Jamshidi Crown Bone Marrow biopsy/Aspiration Needle with… Official notice ↗
Product Pouches may not be sealed properly and compromise the sterility of the device
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Becton Dickinson & Co. medical device recall: Kit BD Max Check-Points CPO IVD EU Official notice ↗
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
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Becton Dickinson & Company medical device recall: BD Vacutainer Lithium HeparinN Official notice ↗
False elevation of carboxyhemoglobin (COHb) results have been reported when using venous blood gas samples collected with tubes analyzed with the IL GEM 4000 instrument.
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Becton Dickinson & Company medical device recall: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part… Official notice ↗
Lot has been confirmed to have no additive within the tube. Sample processed without the preservative (additive) in the tube, testing has yielded reliable results if the…
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Becton Dickinson & Company medical device recall: 3mL Luer-Lok Syringe Official notice ↗
The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and…
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Becton Dickinson & Company medical device recall: BD Microtainer Tube w/ BD Microgard Closure Official notice ↗
The products have been confirmed to have reduced or no additive within the tube reservoir. The tubes may develop visible clots within the tube samples or micro clots…
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Becton Dickinson & Company medical device recall: Alaris Pump Infusion Set Official notice ↗
An incomplete occlusion can be caused by a variation in the wall thickness of the pumping segment of the affected infusion sets used with the. The issue has the…
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Becton Dickinson & Company medical device recall: SmartSite Syringe Administration Set-Product Package Size 50 Official notice ↗
Leaking of the Smartsite Syringe Administration Set. May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to…
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Becton Dickinson & Company medical device recall: BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended… Official notice ↗
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
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Becton Dickinson & Co. medical device recall: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with… Official notice ↗
Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to…
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Becton Dickinson & Company medical device recall: Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07 Official notice ↗
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
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Becton Dickinson & Company medical device recall: BD Blood Collection Assembly with Male Luer Lock Official notice ↗
The luer could break and cause the device to leak or break off and get stuck in the fistula needle port rendering the port inaccessible for dialysis. As a result, the…
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Becton Dickinson & Co. medical device recall: BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage:… Official notice ↗
BD Synapsys version 2.1 allowed the potential for a test order to be associated to an incorrect culture record.
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Becton Dickinson & Co. medical device recall: BD MAX Enteric Bacterial Panel -For In Vitro Diagnostic Use with the… Official notice ↗
False negative results with the BD MAX Extended Enteric Bacterial Panel when testing specifically for Enterotoxigenic Escherichia coli (ETEC) and Plesiomonas…
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Becton Dickinson & Co. medical device recall: Phoenix AST-s Indicator Official notice ↗
Panels inoculated using certain lots of the indicator solution are demonstrating an increased occurrence of test aborts.
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Becton Dickinson & Co. medical device recall: BD BBL Trypticase Soy Agar with 5% Sheep Blood Official notice ↗
a portion of a single lot was not manufactured in accordance with the internal formulation resulting in inhibited growth of Gram negative organisms.
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Becton Dickinson & Company medical device recall: BD Vacutainer Urine Collection Cups Official notice ↗
BD Vacutainer Urine Collection Cups may contribute to a slight elevation of Red Blood Cell (RBC) counts when used with the Sysmex UF Series Analyzers. BD recommends…
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Becton Dickinson & Company medical device recall: PCEA ASV Yellow Microbore Official notice ↗
The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.
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Becton Dickinson & Company medical device recall: BD NEXIVA Closed IV Catheter System Dual Port 18GA 1.25 IN Official notice ↗
One lot of the specified needles is not performing as intended due to a failure in the needle tip shield/safety mechanism, which may lead to an increased risk of a…
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Becton Dickinson & Co. medical device recall: BD Max Instrument Reader Spare Part Official notice ↗
A trend for false positive Candida glabrata results has been confirmed. The discrepant results impact the Candida glabrata target only, when in the presence of a…
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Becton Dickinson & Co. medical device recall: BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station Official notice ↗
The device may not function at the lower end (<15 deg. C) of the labeled operating temperatures. The instrument returns to normal operating conditions when environmental…
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Becton Dickinson & Co. medical device recall: BD BBL GC-Lect Agar Official notice ↗
A portion of this lot was manufactured using Gentamicin instead of Vancomycin. Gentamicin is an inhibitory agent of Neisseria organisms. This product is a selective…
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Becton Dickinson & Company medical device recall: The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an… Official notice ↗
Approximately 3.4% of BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (2.7mL) (light blue top tube) will exhibit over fill draw volumes from ~11-14%.
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Becton Dickinson & Company medical device recall: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL… Official notice ↗
Tubes may exhibit stopper creepout/pullout, where the stopper dissociates from the tube
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Becton Dickinson & Co. medical device recall: Bd Max Dna Mmk Official notice ↗
The package insert incorrectly lists the volume of the primer and probe diluent to use for the reconstitution of the master mix tube. Adding the incorrect amount of…
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Becton Dickinson & Company medical device recall: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 mm x 305 mm… Official notice ↗
Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
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Becton Dickinson & Company medical device recall: BD Vacutainer¿ Barricor" Lithium Heparin Plasma Blood Collection… Official notice ↗
Increased amount of residual blood present on the top of stopper well after venipuncture
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Becton Dickinson & Company medical device recall: BD Vacutainer¿ EDTA Lavender Top Tubes: Catalog Numbers: 1. 366401 Official notice ↗
BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer Lithium Heparin Green Top Tubes can cause an underestimation of lead in blood samples when used…
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Becton Dickinson & Co. medical device recall: Difco" Agar Noble Official notice ↗
HighPuragar was mislabeled and inadvertently sold as Noble Agar.
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Becton Dickinson & Company medical device recall: BD Vacutainer¿ K2 EDTA Official notice ↗
A limited portion of the lot was manufactured with less than the required amount of K2EDTA additive, an anticoagulant, which may cause erroneous results that could lead…
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Becton Dickinson & Co. medical device recall: BD MAXTM Vaginal Panel. Catalog Number(s): 443712 443710 443711 Official notice ↗
BD recently notified customers in July 2017 regarding an increased rate of unresolved (UNR) and indeterminate (IND) results for the BD MAXTM Vaginal Panel, experienced…
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Becton Dickinson & Co. medical device recall: BD PhoenixTM AP Official notice ↗
Potential unexpected movement of robot arm
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Becton Dickinson & Company medical device recall: BD Precision Glide Needle 18G x 1 RB Official notice ↗
Hub damage resulting in breakage and/or leakage during use.
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Becton Dickinson & Co. medical device recall: TrypticaseTM Soy Agar with 5% Sheep Blood Official notice ↗
Listeria monocytogenes contamination of non-sterile plated media
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Becton Dickinson & Company medical device recall: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G Official notice ↗
Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD Ultra-Fine needle ¿mL 12.7mm 30G, Cat (Ref) 328466, was found to have some polybags in the lot…
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Becton Dickinson & Co. medical device recall: BD Phoenix PMIC-107 Official notice ↗
BD has recently confirmed quality control failures, related to a manufacturing issue, for the inducible macrolide-linosamide-streptogramin B (iMLSb) test contained on…
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Becton Dickinson & Company medical device recall: BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride… Official notice ↗
After a receiving a customer complaint for incorrect labeling, BD has confirmed that a portion of SPS tubes associated with catalog 364960, lot 6090812 were incorrectly…
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Becton Dickinson & Company drug recall: ChloraPrep OneStep Official notice ↗
Labeling; Label Mixup; the immediate package is labeled incorrectly as Chloroprep Onestep (Clear), however, the correct label should be Chloroprep with Tint (Hi Lite…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.