Every recall we track for Musculoskeletal Transplant Foundation, Inc. — 5 in all — plus the complaints and injury reports the public filed about them.
Musculoskeletal Transplant Foundation recalls AFT Diverted Tubes (Product Code 227005) that may cause extended surgery time due to extrudability issues. Affected units include specific donor lots.
Musculoskeletal Transplant Foundation recalls AFT bone void filler tubes (Product Code 227010) that may cause extended surgery time due to extrudability issues. Affected units include specific donor lots and UDI-DI numbers.
Musculoskeletal Transplant Foundation recalls DBX Demineralized Bone Matrix Putty labeled 10cc but actually 1cc. This may prolong surgery. Product model 038100 with specific serial numbers.
Musculoskeletal Transplant Foundation recalls AFT Straight Tube (3/4 filled) due to potential surgery delay from improper filling. Affected units have specific lot numbers.
Musculoskeletal Transplant Foundation recalls QuickGraft Model 430PST due to label measurements not accounting for tension, potentially increasing surgical time. Affected units have specific serial numbers listed.
