Snapshot Tracker Kit — Class II medical device recall Z-0721-2020
Terminated recall by Mazor Robotics Ltd, reported 2020-01-01, distributed in AR, AZ, CA, CO, CT, FL, GA, IL…. The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications a
| Recall number | Z-0721-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mazor Robotics Ltd, Caesarea, Israel |
| Recall initiated | 2019-07-02 |
| Classified | 2019-12-20 |
| Reported by FDA | 2020-01-01 |
| Terminated | 2022-02-02 |
| Distributed | AR, AZ, CA, CO, CT, FL, GA, IL, IN, KY, LA, MA, MD, MI, MN, NC, ND, NY, PA, SC, SD, TN, TX, UT, VA, WV |
| Quantity | 93 snapshot |
| UPC / GTIN / UDI-DI | 07290109181868 |
| Lot numbers | 070481, 070490, 070494, 070495, 070496, 070542, 070548, 070551 |
Product
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Reason for recall
The firm has become aware that the Snapshot Trackers were not manufactured in accordance with specifications and could potentially lead to navigational inaccuracies, which may result in patient injury, e.g. nerve damage or neurological deficit/dysfunction
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-0721-2020. 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.