FDAAugust 31, 2020device

AltiVate Reverse Small Socket Insert, 44mm Semi Constrained - E-Plus, Part Number: 509-03-044 - Product Usage: Per IFU, DJO Surgical shoulder devices are intended for treatment of patients who are candidates for shoulder arthroplasty per the Indication for use.

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

The hazard

Product mislabeled. Use may result in a delay in surgery, stopping of surgery, and revision surgery.

What to do

FDA enforcement status: Terminated

Brands named

encore medical lpencoreencore medical

Recall history

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

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