Z-2101-2021 Class II Terminated

Recalled by Stryker Spine — Allendale, NJ

Recall Details

Product Type
Devices
Report Date
July 28, 2021
Initiation Date
May 18, 2021
Termination Date
April 15, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
559 total

Product Description

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

Reason for Recall

The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.

Distribution Pattern

US Nationwide Distribution

Code Information

lots A1903054, A1906006