Bard Access Systems recalls

Bard Access Systems has 65 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 23 Sep 2026. 19 are still ongoing. 17 were reported in the last 12 months.

Total recalls65since 2012
Last 12 months17reported
Class I58% of total
Ongoing19latest 23 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 5 8%Class II 55 85%Class III 5 8%

Why bard access systems is recalled

By year

Ongoing bard access systems recalls

19 active

All bard access systems recalls, newest first

65 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IDuoGlide Short-Term Straight Dialysis Catheter recalledBard Access SystemsOther50 states
DeviceCLASS IPower-Trialysis Short-Term Straight Dialysis Catheter recalledBard Access SystemsOther50 states
DeviceCLASS IBD Needle Kit for Powered Driver recalled by Bard Access SystemsBard Access SystemsOther32 states
DeviceCLASS II5605150 Power-Trialysis Short-Term Straight Dialysis recalledBard Access SystemsOtherNationwide
DeviceCLASS II1174108 PowerPICC Catheter Single-Lumen recalled by Bard Access SystemsBard Access SystemsOtherNationwide
DeviceCLASS II4380 Economy Soft Tissue Biopsy Tray recalled by Bard Access SystemsBard Access SystemsOtherNationwide
DeviceCLASS IICK000980A PowerMidline Catheter Dual-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS II7617408 Groshong NXT ClearVue Catheter Single-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS IIOtp5000 Thora/para Tray, Non-valved recalled by Bard Access SystemsBard Access SystemsOtherNationwide
DeviceCLASS IICK000662 PowerPICC SOLO HF Catheter Triple-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS II1274108D PowerPICC SV Catheter Dual-Lumen REKW2449 recalledBard Access SystemsOtherNationwide
DeviceCLASS IICK000525B PowerPICC Provena SOLO Catheter Dual-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS II5625240 DuoGlide Short-Term Straight Dialysis Catheter Dual-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS IICK000880 Provena Midline Catheter Dual-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS IICK000727 PowerMidline Catheter Single-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS II5855240 Power-Trialysis Slim-Cath Straight Short-Term recalledBard Access SystemsOtherNationwide
DeviceCLASS IICK000495A Poly Midline Catheter Single-Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS IBD Single-Lumen PowerPICC Catheters recalled by Bard Access SystemsBard Access SystemsPackaging DefectsNationwide
DeviceCLASS ID015151NK/BD Needle Kit for Powered Driver recalledBard Access SystemsForeign MaterialNationwide
DeviceCLASS IIPowerPICC Catheter Single-Lumen recalled by Bard Access SystemsBard Access SystemsOther10 states
DeviceCLASS IIIR PowerPICC Convenience Kit Catheter Dual Lumen recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 7617408, Groshong NXT ClearVue Catheter, Full Kit, 4F recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 7812400, Replacement Connector For 4F Groshong NXT clearVue Picc recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF CK000516, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 7617405, Groshong NXT ClearVue Catheter Basic Kit, 4F recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 91660417, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 7617407, Groshong NXT ClearVue Catheter, Full Kit, 4F recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 9655405, Groshong NXT ClearVue Catheter with Sherlock Tip recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 9617407, Groshong NXT ClearVue Catheter with Sherlock Tip recalledBard Access SystemsOtherNationwide
DeviceCLASS IIREF 7617408D, Groshong NXT ClearVue Catheter, Maximal Barrier Kit recalledBard Access SystemsOtherNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.