FDAApril 21, 2026device

Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC; RA CATH KIT: 20 GA X 5 IN/ASK-04020-MW; ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM5; CATH SL 20 GA X 5 CM HYDROPHILIC/ASK-00520-JH; CATH S-L 20 GA X 5 CM HYDROPHILIC/ASK-00520-UHC; ARTERIAL LINE KIT: 20 GA x 5IN/ASK-00820-CL; RA CAT...

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

108019021215511080190219327510801902142983108019021387881080190213983910801902193916108019022059091080190219593410801902138801108019022023041080190211763910801902117936

Recall history

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

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