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Medical Device

Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000

Recall date: 2026-06-24 · Source: FDA_DEVICE
Brand / Firm
ARROW INTERNATIONAL, LLC
Product
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
Reason for recall
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 sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.
Units affected
7560
Description
Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000
View official recall notice →