AFT — Class II medical device recall Z-1066-2024
Ongoing recall by Musculoskeletal Transplant Foundation, Inc., reported 2024-02-21, distributed in MN. Filling process qualification did not demonstrate adequate process capability. Possible consequences include e
| Recall number | Z-1066-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2023-12-22 |
| Classified | 2024-02-09 |
| Reported by FDA | 2024-02-21 |
| Distributed | MN |
| Quantity | 89 |
| Lot numbers | 02921115411127 |
Product
AFT (Allograft Filler Tube) Straight Tube (1/2 Filled), Product Code 227010 (bone void filler)
Reason for recall
Filling process qualification did not demonstrate adequate process capability. Possible consequences include extended surgery time due to extrudability issues.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1066-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.