FDAApril 10, 2023device

stryker ORTHOLOC 3Di Fusion Plate MTP Right, REF 58A220RT, bone stabilization and fixation

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

The hazard

Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion descriptions laser marked on the parts.

What to do

FDA enforcement status: Ongoing

Brands named

wright medical technologywrightwright medical

UPCs

00889797101011

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →