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FDAApril 21, 2026device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

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UPCs

308019021217221080190219327520801902121756

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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