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Musculoskeletal Transplant Foundation, Inc. recalls Musculoskeletal Transplant Foundation, AFT Diverted Tube (3/4/Filled), indicated for treatment of surgically-created oss
Recalled July 13, 2016 · FDA recall Z-2004-2016 · Musculoskeletal Transplant Foundation
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. · FDA Class II
Units
114 units
Sold at
nationwide
Description
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.
Product
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.
Manufacturer(s)
Musculoskeletal Transplant Foundation, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →