FDANovember 17, 2020device

Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System, Thoracolumbosacral pedicle screw system

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

The hazard

Zimmer Biomet is conducting a medical device correction to update the Instructions for Use (IFU) and the Surgical Techniques for the Polaris Spinal System Translation Screw and Cypher MIS Screw System. Users should be aware that changes were made to the contraindications section indicating that the Translation Screws should not be used with a direct current stimulation, as a high probability of construct failure exists when using Translation Screws containing CoCr with direct current simulation system.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

Recall history

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

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