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Stryker Spine Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979 - safety alert
Official notice
28 Jul 2021
Last checked
28 Jul 2021
An official FDA notice concerns Stryker Spine Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979 - safety alert. An official FDA notice concerns Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-07-28. Recall numbers: Z-2101-2021. Check the official notice for the complete list. Published 2021-07-28.
What to do now
The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.
Units affected
559
Recall number
Z-2101-2021
Official notice
2021-07-28
The hazard
The hazard
An official FDA notice concerns Cortoss Bone Augmentation Material 10cc Cartridge, Catalog Number 2101-0010, GTIN 00808232000979. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2021-07-28. Recall numbers: Z-2101-2021. Check the official notice for the complete list.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Recall Numbers
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Affected products
Product 1
Units affected
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Affected area 2
Company & contacts
Company & contacts
Brand: Stryker Spine. Contact: Stryker Spine.
Source & status
Source & status
Recall details
Recall details
Recall number
Event id
Units affected
Status
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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