Home / Recalls / Medical Devices
Stryker GmbH recalls Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Recalled July 18, 2018 · FDA recall Z-2393-2018 · 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
12
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
Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
Manufacturer(s)
Stryker GmbH
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →