Reported Jan 1, 2020 · Terminated

Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

Mazor Robotics Ltd.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Mazor Robotics Ltd · North Industrial Park · Caesarea · N/A

Is this the product you have?

  • Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile
  • UDI07290109181868
Lot codes and dates
  • Lot Numbers
    • 070494
    • 070548
    • 070551
    • 070481
    • 070490
    • 070495
    • 070542
    • 070496
Amount recalled
93 snapshot trackers

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Mazor Robotics Ltd. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 2, 2022 · Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.