NavLock Tracker *** Rx Only — Class II medical device recall Z-1693-2020
Terminated recall by Medtronic Navigation, Inc., reported 2020-04-22, distributed in NY. Product was incorrectly assembled which could affect navigation accuracy of the device.
| Recall number | Z-1693-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Navigation, Inc., Louisville, CO, United States |
| Recall initiated | 2019-08-28 |
| Classified | 2020-04-10 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2021-05-05 |
| Distributed | NY |
| Quantity | 1 units |
| UPC / GTIN / UDI-DI | 00763000123185 |
| Serial numbers | 000012585 |
Product
NavLock Tracker *** Rx Only
Reason for recall
Product was incorrectly assembled which could affect navigation accuracy of the device.
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-1693-2020. 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.