FDAApril 27, 2018device
Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The manufacturer has discovered that potentially out-of-specification products may have left the factory. Non-conforming cannulation of the nails may result in reduced component strength and potentially premature nail breakage.
What to do
FDA enforcement status: Terminated
Brands named
stryker
UPCs
04546540673398
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- FDADaig Livewire Steerable, Product Number 401603, REPROCESSED ELECTROPHYSIOLOGY CATHETER2026-04-10
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