FDAApril 21, 2026device

Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A; RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-X1A; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-HCA; ARTERIAL CATHETER KIT: 18 GA X 16 CM/ASK-04018-UPM; RA CATH KIT: 20 GA X 1-3/4IN/ASK-04020-HC; ARTERIAL LINE KIT: 20 GA X 5IN (12 CM)/ASK-04020...

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

108019021932751080190211926850801902117644108019021213841080190211769110801902117769108019021178371080190212492710801902117929108019021140411080190211800110801902118025

Recall history

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

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