# FDA recall Z-1693-2020

> **Medtronic Navigation, Inc.** · Class II · device recall initiated 2019-08-28.

## 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

- **Recall number:** Z-1693-2020
- **Recalling firm:** Medtronic Navigation, Inc.
- **Classification:** Class II
- **Product type:** device
- **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

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1693-2020

## Citation

> AI Analytics. FDA recall Z-1693-2020. Retrieved 2026-07-13 from https://api.ai-analytics.org/recall/Z-1693-2020. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*