Recall database

Catheter, Hemodialysis, Triple Lumen, Non-Implanted recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–3 of 3 recalls

Class IIOngoingZ-2661-2026

Bard Access Systems, Inc. recalls 5855240 Power-Trialysis Slim-Cath Straight Short-Term Dialysis Catheter 12 Fr Triple-Lu…

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

Bard Access Systems, I…UTJul 8, 2026

Class IIOngoingZ-2660-2026

Bard Access Systems, Inc. recalls 5605150 Power-Trialysis Short-Term Straight Dialysis Catheter 13 Fr Triple-Lumen UDI-D…

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

Bard Access Systems, I…UTJul 8, 2026

Class IOngoingZ-2374-2026

ARROW INTERNATIONAL, LLC recalls Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if ster…

ARROW INTERNATIONAL, L…NCJun 24, 2026