Home / Recalls / Medical Devices
Zimmer CAS recalls Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
Recalled June 10, 2015 · FDA recall Z-1701-2015 · Zimmer CAS
Hazard
Zimmer CAS has determined that the potential exists for the spikes on the iASSIST Tibial Alignment Guide to bend or break during insertion or extraction from the tibia during use. · FDA Class II
Units
78 devices
Sold at
Nationwide Distribution including AL, AZ, CA, CA, CO, FL, IN, MI, NJ, NY, OH, OR, PA, TX, VA, and WI.
Description
Zimmer CAS has determined that the potential exists for the spikes on the iASSIST Tibial Alignment Guide to bend or break during insertion or extraction from the tibia during use.
Product
Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;
Manufacturer(s)
Zimmer CAS
Made in
Canada
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →