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FDADecember 22, 2023device

AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)

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

The hazard

Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.

What to do

FDA enforcement status: Ongoing

Brands named

musculoskeletal transplant foundationmusculoskeletalmusculoskeletal transplant

UPCs

0032202924113700322039641144

Recall history

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

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