FDAApril 2, 2020device

OSTEOVATION RMX 10 CC Injectable. REF/UDI: 390-6002/ /00813845021099 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.

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

The hazard

Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.

What to do

FDA enforcement status: Terminated

Brands named

osteomed

UPCs

00813845021099

Recall history

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

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