FDANovember 10, 2015device

UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is intended for immobilization and stabilization of the posterior, non-cervical spine in skeletally mature patients as an adjunct to fusion for the following indications: degenerative disc disease (defined...

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

The hazard

Response Spine UniAxial Pedicle & UniAxial Reduction Pedicle Screws may have been manufactured incorrectly, thus preventing the driver from fully engaging into the hexagonal drive feature of the screw.

What to do

FDA enforcement status: Terminated

Brands named

orthopediatrics

Recall history

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

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