Bard Access Systems, Inc.

Frequent Recalls

14

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-07-08 to 2026-07-08

Date	Source	Product	Brand	Severity	Units
2026-07-08	FDA Device	FDA Recall: 7617408 Groshong NXT ClearVue Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741035258 The Grosh	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 P4254108 PowerMidlin	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 4380 ECONOMY SOFT TISSUE BIOPSY TRAY UDI-DI Code: 0110885403108563 4382A SOFT TISSUE BIOPSY TRAY	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 1174108 PowerPICC Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741154935 1295108 PowerPICC SOLO	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-DI Code: 00801	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 CK000566 Poly Midl	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lumen UDI-DI C	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 CK000729 PowerMidli	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000880 Provena Midline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188770 S4153108BDP Proven	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code: 00801741042119	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 P	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 3173108D PowerPICC SV Cathet	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 Catheter st	Bard Access Systems, Inc.	Class II	N/A
2026-07-08	FDA Device	FDA Recall: OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS	Bard Access Systems, Inc.	Class II	N/A

Bard Access Systems, Inc. Recalls | WatchRecall