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Stryker GmbH recalls Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
Recalled July 18, 2018 · FDA recall Z-2398-2018 · 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
Units
7
Sold at
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
Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →