FDA recall Z-0963-2026

Howmedica Osteonics Corp. · Class II · device

Product

The Stryker CranialMask Tracker is a single-use device consisting of a flexible printed circuit board (PCB) with 31 infrared (IR) light-emitting diodes (LEDs) as well as an electronics control unit for the LEDs which includes its own battery power supply. The measured LED positions can be used in one of three different modes of operation: Patient tracking, Registration using surface matching, and Automatic intra-operative mask registration.

Reason for recall

When the device is activated during surgery, the device software issues an error message "Instrument Face Mask (6001385000000) is not valid for this application" resulting in an inability to use the device.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Germany, Japan, South Korea.

Key facts

Status
Ongoing
Initiation date
2025-11-12
Report date
2025-12-31
Voluntary/Mandated
Voluntary: Firm initiated
Location
Mahwah, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0963-2026