Recall archive
6 recalls · page 1 of 1
Reported Sep 23, 2026
Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
Matched: Brand — this is a downstream recall of class I recall RES 98777
1 more product in this recall
FDA (weekly enforcement report)
Reported Aug 26, 2026Updated Sep 7, 2026
BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
Matched: Brand · Reason for recall — After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically…
FDA (openFDA device enforcement)
Reported Jul 8, 2026
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems, Inc.
Matched: Brand — Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled…
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 23, 2025
BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
Matched: Brand · Reason for recall — Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher),…
FDA (openFDA device enforcement)
Reported Aug 3, 2022
Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
Matched: Brand · Reason for recall — BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal…
FDA (openFDA device enforcement)
Reported Dec 10, 2014
GuardIVa Antimicrobial Hemostatic IV Dressing, REF FP-23-AD008, Manufacturer: Bard Access Systems, Inc. USA. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems
Matched: Brand · Product · Product details · Reason for recall — Bard Access Systems is recalling GuardIVa (Ref. No. FP23AD006) from lot ASXHT003 because they were non-sterile unit samples which potentially could…
FDA (openFDA device enforcement)
RecallNow is not a government agency. Every notice above is published by the FDA, USDA FSIS, or CPSC and links back to its source. Back to the look-up