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Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Smooth-Tipped, 2.2 x 800mm Product Usage: Intended for the temporary stabilization of bone se
Recalled March 2, 2016 · FDA recall Z-0880-2016 · Stryker Howmedica Osteonics
Hazard
During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased. · FDA Class II
Units
147,838 units in total
Sold at
US Nationwide Distribution
Description
During a review of the packaging, it was determined that the seal integrity of the pouch may be decreased.
Product
Stryker, T2 Guidewire, Smooth-Tipped, 2.2 x 800mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.
Manufacturer(s)
Stryker Howmedica Osteonics Corp.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →