Bard Access Systems recalls
23 recalls in our records from 2012 to 2026: 23 FDA medical devices.
Recalls with full detail pages
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Bard Access Systems, Inc. medical device recall: Power-Trialysis Short-Term Straight Dialysis Catheter
this is a downstream recall of class I recall RES 98777
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Bard Access Systems, Inc. medical device recall: BD Needle Kit for Powered Driver 15mm x 15Ga
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases,…
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Bard Access Systems, Inc. medical device recall: BD 4 Fr Single-Lumen PowerPICC Catheters
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to…
Earlier and other recalls
These link to the official agency notice.
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Bard Access Systems, Inc. medical device recall: Otp5000 Thora/Para Tray Official notice ↗
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
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Bard Access Systems, Inc. medical device recall: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD… Official notice ↗
BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire…
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Bard Access Systems Inc. medical device recall: 5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm… Official notice ↗
Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.
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Bard Access Systems Inc. medical device recall: 5Fr PowerPICC Catheter Single-Lumen with 70cm Guidewire Instructions… Official notice ↗
Catheter kits contained the incorrect micro-introducers.
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Bard Access Systems Inc. medical device recall: Ref 7617400 Official notice ↗
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the…
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Bard Access Systems Inc. medical device recall: PowerPICC Provena Catheters Official notice ↗
Possible leaks on the 3 Fr. Single lumen and 4 Fr. Dual lumen PowerPICC catheters at the luer hub extension leg junction.
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Bard Access Systems Inc. medical device recall: StatLock¿ IV Premium Catheter Stabilization Device Official notice ↗
StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.
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Bard Access Systems medical device recall: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product… Official notice ↗
Bard Access Systems announces a voluntary field action for the SafeStep¿ Huber Needle Set with Y-Injection Site and MiniLoc¿ Safety Infusion Set Winged without…
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Bard Access Systems medical device recall: StatLock¿ PICC Plus Crescent Foam. Product Code: VPPCSP & VPPCSPCE.… Official notice ↗
Bard Access Systems announces a voluntary field action for the StatLock¿ Catheter Stabilization Devices because some single unit pouches have been released without…
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Bard Access Systems medical device recall: Marketing brochures for the PowerPICC and PowerPICC SOLO catheters Official notice ↗
Bard Access Systems is recalling marketing brochures for the PowerPICC¿ and PowerPICC¿ SOLO¿ catheters due to incorrect indication for use contained in the brochure.
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Bard Access Systems medical device recall: PowerPICC SOLO Catheter with Sherlock 3CG TPS Stylet 4F Maximal… Official notice ↗
Bard Access Systems is recalling PowerPICC Solo Catheter Kits due to incorrect expiration dates on the primary labeling.
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Bard Access Systems medical device recall: PowerLoc MAX Safety Winged Infusion Set Official notice ↗
Bard Access Systems is conducting a field action due to the potential that an incorrect Maximum Flow rate label associated to the power injection IFU for the PowerLoc…
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Bard Access Systems medical device recall: Bard Peripherally Inserted Central Catheter Official notice ↗
Potential for inadvertent scalpel stick injury involving the safety scalpel.
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Bard Access Systems medical device recall: BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following… Official notice ↗
Some unit packages of BD PosiFlush SF Saline Flush Syringe 10 mL may exhibit open seals, which could impact product sterility. Bard includes these pouched syringes,…
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Bard Access Systems medical device recall: GuardIVa Antimicrobial Hemostatic IV Dressing Official notice ↗
Bard Access Systems is recalling GuardIVa (Ref. No. FP23AD006) from lot ASXHT003 because they were non-sterile unit samples which potentially could be used clinically.
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Bard Access Systems medical device recall: PowerPort Slim Implantable Port Official notice ↗
Labeling discrepancy.The label states that the implantable port contains silicone suture plugs, however approximately 23% of the units contained in the affected lots…
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Bard Access Systems medical device recall: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone… Official notice ↗
Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single Lumen Broviac Catheter because a small number of Silicone catheters in the may be undersized…
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Bard Access Systems medical device recall: StatLock CV Plus w/Pigtail Official notice ↗
BARD Access Systems is recalling lot JUWJF283 of StatLock CV Plus Stabilization Butterfly Devices due to incorrect pad assembly used during manufacture. The absence of…
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Bard Access Systems medical device recall: Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth… Official notice ↗
Bard Access Systems is recalling two lots of Hickman 9.0 French and one lot of Leonard 10.0 French Dual Lumen Catheters with SureCuff Tissue Ingrowth Cuff with…
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Bard Access Systems medical device recall: 16 Fr HemoStar XK Long-Term Hemodialysis Catheter Official notice ↗
Bard Access Systems is recalling one lot of 16 Fr HemoStar XK Long Term Hemodialysis Catheters because they were identified with an incorrect expiration date, 03/2015…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.