Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS — Class II medical device recall Z-2047-2017
Terminated recall by Medtronic Sofamor Danek USA Inc, reported 2017-05-17. Product packaging may incorrectly include two bevel-tipped needles or two trocar-tipped needles instead of one
| Recall number | Z-2047-2017 |
|---|---|
| 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 | 2017-04-13 |
| Classified | 2017-05-05 |
| Reported by FDA | 2017-05-17 |
| Terminated | 2017-12-28 |
| Countries outside the US | BE, DE, ES, FR, IT, JP |
| Quantity | 36 units |
| Lot numbers | 0521148W |
| Model numbers | 8670009 |
| Expiration dates | 2021-10-21 |
Product
Medtronic PAK NEEDLE BEVELED AND TROCAR TIPS, REF 8670009, QTY 1 EA, STERILE R, Rx only
Reason for recall
Product packaging may incorrectly include two bevel-tipped needles or two trocar-tipped needles instead of one diamond-tipped needle and one bevel-tipped needle.
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-2047-2017. 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.