Stryker Spine recalls Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Nu
Recalled Product
Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
Hazard / Issue
The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: lot A1908003
View official government recall
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