AFT Straight Tube — Class II medical device recall Z-1562-2021
Terminated recall by Musculoskeletal Transplant Foundation, Inc., reported 2021-05-19, distributed nationwide. 3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery
| Recall number | Z-1562-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Musculoskeletal Transplant Foundation, Inc., Edison, NJ, United States |
| Recall initiated | 2021-03-29 |
| Classified | 2021-05-12 |
| Reported by FDA | 2021-05-19 |
| Terminated | 2023-04-27 |
| Distributed | Nationwide (US) |
| Quantity | 672 units |
| UPC / GTIN / UDI-DI | 00319022171149 |
| Serial numbers | 00319018541145, 00319022171149, 00419019631149, 03818070421114, 09819009071105, 09819036171142 |
| Model numbers | 227007 |
Product
AFT Straight Tube (3/4 Filled) - Human Allograph Tissue for treatment of surgically-created osseous defects or osseous defects created from traumatic injury. It can be used in the: extremities, pelvis, and spine Item Number: 227007
Reason for recall
3/4 AFT Straight Fill Tubes (227007) filled only 1/2 way instead of 3/4, may cause delay of surgery
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-1562-2021. 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.