FDAMarch 3, 2025device

stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented

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

The hazard

A specific lot of Latitude Humeral Trial Stems has the incorrect direct part marking. " Laser Marked: 9030103, Humeral Stem Trial 150mm Large / Right, Yellow color indicator (incorrect) " Device Actually: 9030092, Humeral Stem Trial 150mm Medium / Left, Red color indicator (correct)

What to do

FDA enforcement status: Ongoing

Brands named

tornier

UPCs

00846832015054

Recall history

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

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stryker Latitude EV HUMERAL REVISION STEM TRIAL, L: 150mm, Size: LARGE, Side: RIGHT, REF 9030103; Prosthesis, Elbow, Semi-Constrained, Cemented — Recall Details · AllClear