Mazor Robotics Ltd: Medical Device Recall in 2020 - (Recall #: Z-0721-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 2, 2019

Date Posted: January 1, 2020

Recall Number: Z-0721-2020

Event ID: 84328

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

Status: Terminated

Product Quantity: 93 snapshot trackers

Code Information:

Lot Numbers: 070494, 070548, 070551, 070481, 070490, 070495, 070542, 070496

Distribution Pattern:

US: Arizona, Arkansas, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, New York, North Carolina, North Dakota, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, West Virginia

Voluntary or Mandated:

Voluntary: Firm initiated