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FDA (Device enforcement)Recalled 2025-08-28class ii

Howmedica Osteonics Corp.: 1. EXETER V40 STEM 44MM NO 2, Model/Catalog Number: 0580-1-442; 2. EXETER V40 STEM 37.5MM NO 0, Model/Catalog Number: 0580-1-352;

Hazard

a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.

Details from the source

Reason for recall: a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted. Distribution: International distribution in the country of United Kingdom. Quantity: 55 units (all OUS) Lot/code info: 1. Model/Catalog Number: 0580-1-442, UDI-DI: 04546540153319, Lot Number: A00976; 2. Model/Catalog Number: 0580-1-352, UDI-DI: 04546540153241, Lot Number: G8754849;

UPC codes

04546540153319, 04546540153241

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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