Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0721-2020 — Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868

U.S. FDA — Device Enforcement · Israel · 2019-07-02 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0721-2020
Date of alert
2019-07-02
Country / jurisdiction
Israel
Risk level
Class II
Risk type
recall
Brand
Mazor Robotics Ltd
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
07290109181868
Reported risk: 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
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.