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FDAApril 19, 2015device

Tibial Alignment Guide; Orthopedic Stereotaxic Instrument;

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Terminated

Brands named

zimmer caszimmer

UPCs

20801101300

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Tibial Alignment Guide; Orthopedic Stereotaxic Instrument; — Recall Details · AllClear