FDASeptember 6, 2023device

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

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

The hazard

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

What to do

FDA enforcement status: Ongoing

Brands named

encore medical lpencoreencore medical

UPCs

00888912144391

Recall history

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

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RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device. — Recall Details · AllClear