FDAOctober 5, 2023device

REF 130-03-738, All-Poly e + Patella, Domed Tri-Peg, 9x38mm, STERILE H2O2

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

The hazard

Mislabeling

What to do

FDA enforcement status: Completed

Brands named

encore medical lpencoreencore medical

UPCs

00888912108560

Recall history

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

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