FDA recall Z-1693-2020
Medtronic Navigation, Inc. · Class II · device
Product
NavLock Tracker *** Rx Only
Reason for recall
Product was incorrectly assembled which could affect navigation accuracy of the device.
Distribution
U.S.: NY No O.U.S.
Key facts
- Status
- Terminated
- Initiation date
- 2019-08-28
- Report date
- 2020-04-22
- Termination date
- 2021-05-05
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Louisville, CO, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1693-2020