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Stryker Spine recalls Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
Recalled July 28, 2021 · FDA recall Z-2101-2021 · Stryker Spine
Hazard
The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution. · FDA Class II
Units
559 total
Sold at
US Nationwide Distribution
Description
The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
Product
Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979
Manufacturer(s)
Stryker Spine
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →