FDAApril 30, 2026device

Halyard, Drape Pack. Kit Code: LMDP36-01.

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

The hazard

Inadvertent distribution of sealed pouches that had not undergone validated sterilization.

What to do

FDA enforcement status: Ongoing

Brands named

avid medicalavid

UPCs

10809160479148

Recall history

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

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