VERTEX SELECT MULTI AXIAL SCREW — Class II medical device recall Z-1941-2020
Terminated recall by Medtronic Sofamor Danek USA Inc, reported 2020-05-20, distributed nationwide. Nonconforming product; length of the product measured shorter than the labeled length.
| Recall number | Z-1941-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Sofamor Danek USA Inc, Memphis, TN, United States |
| Recall initiated | 2020-03-26 |
| Classified | 2020-05-08 |
| Reported by FDA | 2020-05-20 |
| Terminated | 2021-03-26 |
| Distributed | Nationwide (US) |
| Quantity | 83 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00613994354686 |
| Lot numbers | H5517628 |
Product
VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
Reason for recall
Nonconforming product; length of the product measured shorter than the labeled length.
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-1941-2020. 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.