FDAJuly 2, 2019device
Snapshot Tracker Kit, Mas2659-01, KIT0898, Rx Only, Non Sterile, UDI: 07290109181868
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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
What to do
FDA enforcement status: Terminated
Brands named
mazor roboticsmazor
UPCs
07290109181868
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAMazor X robotic guidance system REF: TPL00592025-12-10
- FDAMazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument2024-07-17
- FDAMAZOR X robotic guidance system, Model TPL0059, with software versions 4.2.2 or 5.0.12023-09-05
- FDATrexo Device2023-05-31
- CPSCModular Robotics Recalls Rechargeable Battery Packs Due to Burn Hazard2020-04-30
- FDAi.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number E4544482016-11-23
- FDACarousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative Kit (KIT0295), accessory used with the Renaissance System (TPL0038). Indicated for precise positioning of surgical instruments or spinal implants during general spinal and brain surgery. It is intended to be used whenever...2014-11-26
Own something like this?
AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.
Start free — 200 items, no card →