Mazor Robotics recalls Snapshot Tracker Kit (Lot Numbers 070494-070548) due to potential navigational inaccuracies that could cause patient injury like nerve damage. Affected users should contact for remedy.
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
Mazor Robotics is recalling its Snapshot Tracker Kit (model Mas2659-01, KIT0898) because it may not be manufactured correctly, which could lead to patient injuries such as nerve damage. This recall affects medical devices used in procedures requiring precise navigation.
The Snapshot Tracker Kit may not be manufactured to specifications, leading to navigational inaccuracies during surgery. This could cause the device to misalign with the patient's anatomy, potentially resulting in nerve damage or neurological issues.
Medical professionals using the Snapshot Tracker Kit for surgical procedures are most at risk. Patients undergoing surgery with this device may experience injury if the device causes navigational errors.
Check for the model number Mas2659-01, KIT0898, and lot numbers 070494 through 070548 on the device packaging or label. The device is only for prescription use and is non-sterile.
Reach out to Mazor Robotics directly for instructions on how to return or replace the device.
The recall indicates potential navigational inaccuracies that could cause patient injury, so it is not safe to use without replacement.
Lot numbers 070494, 070548, 070551, 070481, 070490, 070495, 070542, 070496 are affected.
Contact Mazor Robotics directly for instructions on returning or replacing the device.
We’ve drafted a message you can send Mazor Robotics to request your refund or repair — edit it as you like.
Subject: Recall Z-0721-2020 — Mazor Robotics Mazor Robotics Hello, I own a Mazor Robotics that is covered by recall Z-0721-2020 from Mazor Robotics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
