medical Class II Updated 2021-07-28

Stryker Spine recalls Cortoss Bone Augmentation Material 10cc Cartridge, Catalog N

Recalled Product

Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979

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: lots A1903054, A1906006
View official government recall

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