Medtronic ANGLED DRILL — Class II medical device recall Z-0566-2018
Terminated recall by Medtronic Sofamor Danek USA Inc, reported 2018-02-21, distributed in MN, NC. Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than wha
| Recall number | Z-0566-2018 |
|---|---|
| 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 | 2017-12-22 |
| Classified | 2018-02-09 |
| Reported by FDA | 2018-02-21 |
| Terminated | 2018-07-31 |
| Distributed | MN, NC |
| Quantity | 2 units |
| UPC / GTIN / UDI-DI | 00643169363502 |
| Lot numbers | EM17F015 |
| Model numbers | 6630902 |
Product
Medtronic ANGLED DRILL, REF 6630902, QTY: 1 EA Rx only
Reason for recall
Medtronic has discovered the product lot in question was noted as having a longer drill tip extension than what is indicated on the print specification.
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-0566-2018. 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.