Bard Access Systems, Inc.: 18 recalls on record

Recalls filed with 1 agency: FDA (18).

First recall on record: May 31, 2017. Most recent: September 23, 2026.

Risk classification: Class I: 3 · Class II: 15

Most recent recalls

DateAgencyProduct
September 23, 2026FDADuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straig…Z-2985-2026
September 23, 2026FDAPower-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Sh…Z-2984-2026
August 26, 2026FDABD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered …Z-2872-2026
July 8, 2026FDA5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI …Z-2660-2026
July 8, 2026FDA7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 …Z-2665-2026
July 8, 2026FDACK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729…Z-2662-2026
July 8, 2026FDA4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE …Z-2668-2026
July 8, 2026FDACK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 …Z-2664-2026
July 8, 2026FDA5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lume…Z-2661-2026
July 8, 2026FDA5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 008…Z-2657-2026
July 8, 2026FDAOTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-…Z-2655-2026
July 8, 2026FDACK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 …Z-2658-2026
July 8, 2026FDACK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 …Z-2663-2026
July 8, 2026FDA1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPIC…Z-2659-2026
July 8, 2026FDACK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK00056…Z-2656-2026
July 8, 2026FDA1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 Powe…Z-2666-2026
July 8, 2026FDACK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S415310…Z-2667-2026
May 31, 2017FDAStatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packag…Z-2120-2017

Questions about this company

How many recalls does Bard Access Systems, Inc. have?
Recalert has 18 U.S. recalls on record for Bard Access Systems, Inc., published between May 31, 2017 and September 23, 2026.
What was the most recent Bard Access Systems, Inc. recall?
FDA recall Z-2985-2026, published September 23, 2026: DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625150; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625200; DuoGlide Short-Term Straight Dialysis Catheter, REF: 5625240; DuoGlide S…
Which agencies have handled Bard Access Systems, Inc. recalls?
Bard Access Systems, Inc. appears as the recalling firm in recalls from: FDA (18).

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