FDAJuly 12, 2023device

IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar

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

The hazard

There is a potential for a product packaging non-conformity issue which presents as a pinhole in either the inner or outer pouch.

What to do

FDA enforcement status: Ongoing

Brands named

medicrea

UPCs

03613720264439

Recall history

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

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IMPIX ALIF S/A, REF number B15241415; intervertebral fusion device - lumbar — Recall Details · AllClear