Class II
Medical Device Recall: AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Musculoskeletal Transplant Foundation, Inc. · December 22, 2023
Reason for Recall
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Distribution
Product was distributed to Minnesota.
Quantity Affected
89
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1066-2024
Status: ongoing
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