FDA Device recall Z-1693-2020
NavLock Tracker *** Rx Only
- FDA Device
- Class II
- terminated
- Published 2020-04-22
On 2020-04-22 the FDA classified a Class II recall of NavLock Tracker *** Rx Only by Medtronic Navigation, citing product was incorrectly assembled which could affect navigation accuracy of the device.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1693-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-28 |
| Published | 2020-04-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Medtronic Navigation |
| Distribution | NY |
Product
NavLock Tracker *** Rx Only
Reason
Product was incorrectly assembled which could affect navigation accuracy of the device.
Identifiers
| code_info | Product Number: 9736061 UDI (GTIN/UPN): 00763000123185 Serial Number: 000012585 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Other recalls by Medtronic Navigation
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FDA Device · Class II · 2024-10-16 · Medtronic Navigation - Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only
FDA Device · Class I · 2024-05-15 · Medtronic Navigation - Medtronic, REF 9733235, Pin, 100mm, STERILE, PERCUTANEOUS
FDA Device · Class II · 2024-01-17 · Medtronic Navigation - Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS
FDA Device · Class II · 2024-01-17 · Medtronic Navigation
All Medtronic Navigation recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1693-2020%22
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