Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Prod
Recalled Product
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Hazard / Issue
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Issued by
FDA
Distribution: Product was distributed to Minnesota.
Lot/Code Info: UDI-DI: W4184227005T0473 Donor Lots 00322029241137 and 00322039641144
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