FDAFebruary 2, 2023device

ORTHOLOC 3DSi CLAW II 4 HOLE Plate, Size 25MM, REF 402S0425, Bone fixation device

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

The hazard

Stryker has identified an issue that impacts two specific lots of CLAW" II plates. The plates within these two lots were found to have been comingled, resulting in the incorrect product in packages. Packaging for 402S0425 incorrectly contained 40241425, and vice versa.

What to do

FDA enforcement status: Ongoing

Brands named

wright medical technologywrightwright medical

UPCs

00840420152985

Recall history

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

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