Recall Atlas

Bard Access Systems recalls

5 official recalls and safety alerts involving Bard Access Systems since 2022-08, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Bard Access Systems or the relevant agency.

  1. 2026-09-23
  2. US
    Drugs & medicalClass I

    Bard Access Systems, Inc. recalls Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis Catheter, REF:…

    this is a downstream recall of class I recall RES 98777

    FDA · DeviceBard Access Systems, Inc.US: FL, IL, OH, VA, MD, TX, WI, GA, TN, IN, SC, NC, MI, PA, OR, OK, AZ, MS,…Official notice →
  3. 2026-08-26
  4. US
    Drugs & medicalClass I

    Bard Access Systems, Inc. recalls BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF: D015251NK, BD Needle…

    After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove…

    FDA · DeviceBard Access Systems, Inc.US: MA, FL, IA, SC, IL, NY, UT, NJ, ID, IN, PA, CA, TX, OH, MO, VA, MD, NC,…Official notice →
  5. 2026-07-08
  6. US
    Drugs & medicalClass II

    Bard Access Systems, Inc. recalls CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midline Catheter 4 Fr Single-Lumen UDI-DI…

    Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

    FDA · DeviceBard Access Systems, Inc.Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR,…Official notice →
  7. 2025-04-23
  8. US
    Drugs & medicalClass I

    Bard Access Systems, Inc. recalls BD 4 Fr Single-Lumen PowerPICC Catheters, REF: 3174155, CK000540, 3174118, CK000483, 3174335, 3174355, CK000196, 9174118, CK000955,…

    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 increased material fatigue leaks, which could lead to…

    FDA · DeviceBard Access Systems, Inc.Worldwide - US Nationwide distribution including in the states of WI, NC, TX,…Official notice →
  9. 2022-08-03
  10. US
    Drugs & medicalClass I

    Bard Access Systems, Inc. recalls Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual…

    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 needle assembly and loss of intraosseous access; 2)…

    FDA · DeviceBard Access Systems, Inc.Distribution US nationwide and Canada.Official notice →