Musculoskeletal Transplant Foundation, Inc.: Medical Device Recall in 2016 - (Recall #: Z-2004-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: April 21, 2016

Date Posted: July 13, 2016

Recall Number: Z-2004-2016

Event ID: 74263

Reason for Recall:

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.

Status: Terminated

Product Quantity: 114 units

Code Information:

Serial 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122 04314046801122

Distribution Pattern:

nationwide

Voluntary or Mandated:

Voluntary: Firm initiated