FDAJuly 23, 2021device

AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343

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

The hazard

The kit contains the wrong vial tray in the package.

What to do

FDA enforcement status: Terminated

Brands named

biomimetic therapeuticsbiomimetic

Recall history

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

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AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343 — Recall Details · AllClear