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Recall Observatory FDA recall evidence

Device product

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;

Z-2640-2025

August 28, 2025

Class II

Product summary

Firm
Howmedica Osteonics Corp.
Event
Event 97559
Status
Ongoing
Classification
Class II
Quantity
55 units (all OUS)
Official record key
device-enforcement:Z-2640-2025

Official wording

Reason: 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.

Code information: 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;

Distribution pattern: International distribution in the country of United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.