Musculoskeletal Transplant Foundation, Inc.
3 federal recalls on file. We monitor every CPSC, FDA, USDA, and NHTSA notice for Musculoskeletal Transplant Foundation, Inc. and translate it into plain English — free weekly digest, optional same-day alerts.
- 2024-02-21FDA-DeviceClass IIAFT (Allograft Filler Tube) Diverted Tube (3/4 Filled), Product Code 227005 (bone void filler)
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
- 2024-02-21FDA-DeviceClass IIAFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
- 2023-11-29FDA-DeviceClass IIDBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of surgically created osseous defects or osseous defects created from traumatic injury. Model Number: 038100
Units are labeled as 10cc; however the units have a fill volume of 1cc units. This may result in prolongation of surgery.
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