FDAApril 21, 2016device

Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine. Product Code: 227005.

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

The hazard

AFT Diverted Tubes are being recalled due to a customer complaint involving one unit which had an unsealed Tyvek pouch. The non-sterile foil pouch may introduce contamination into the sterile field.

What to do

FDA enforcement status: Terminated

Brands named

musculoskeletal transplant foundationmusculoskeletalmusculoskeletal transplant

UPCs

04314046801122

Recall history

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

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