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Recall Observatory FDA recall evidence

Device product

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

Z-2101-2021

May 18, 2021

Class II

Product summary

Firm
Stryker Spine
Event
Event 88217
Status
Terminated
Classification
Class II
Quantity
559 total
Official record key
device-enforcement:Z-2101-2021

Official wording

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

Code information: lots A1903054, A1906006

Distribution pattern: US Nationwide Distribution

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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