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Stryker GmbH recalls Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Recalled July 18, 2018 · FDA recall Z-2407-2018 · Stryker
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. · FDA Class II
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The products were distributed to the following US states: AL, Co, FL, KY, NC, TN, UT, and WA.
Description
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.
Product
Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →