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Musculoskeletal Transplant Foundation, Inc. recalls AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Recalled February 21, 2024 · FDA recall Z-1067-2024 · Musculoskeletal Transplant Foundation
Hazard
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues. · FDA Class II
Units
50
Sold at
Product was distributed to Minnesota.
Description
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Product
AFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Manufacturer(s)
Musculoskeletal Transplant Foundation, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →