Recall database

Catheter, Hemodialysis, Non-Implanted recalls

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

Showing 1–2 of 2 recalls

Class IOngoingZ-2373-2026

ARROW INTERNATIONAL, LLC recalls Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F

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…

Non-Implanted Hemodialysis Catheter
Nonconforming Material/Component

ARROW INTERNATIONAL, L…NCJun 24, 2026

Class IIOngoingZ-2319-2026

Mozarc Medical US LLC recalls Mahurkar Elite PASS Trays

The Tegaderm CHG dressing, as specified in product labeling, was missing from certain lots of Mahurkar Elite PASS Trays.

Non-Implanted Hemodialysis Catheter
Under Investigation by firm

Mozarc Medical US LLCMAJun 17, 2026