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Conformis, Inc. recalls iTotal Identity Posterior Stabilised (PS) Knee Replacement System Model Number: TPS-301-1113-020101
Recalled April 20, 2022 · FDA recall Z-0899-2022 · Conformis
Hazard
Incorrect tibial base plate implant packaged in kit · FDA Class II
Units
1 unit
Sold at
MS
Description
Incorrect tibial base plate implant packaged in kit
Product
iTotal Identity Posterior Stabilised (PS) Knee Replacement System Model Number: TPS-301-1113-020101
Manufacturer(s)
Conformis, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →