FDAApril 3, 2025device

MAGEC 2 Rod, 5.0mm 90mm Standard; Version/Model: MC2-5090S;

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

The hazard

Devices for the affected lot were not assembled according to product specifications. The distraction rod outer diameter was assembled with a 5.5mm rod versus the required 5.0mm.

What to do

FDA enforcement status: Ongoing

Brands named

globus medicalglobus

UPCs

00887517834041

Recall history

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

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