Cortoss Bone Augmentation Material 5cc Cartridge recall
Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
Why was Cortoss Bone Augmentation Material 5cc Cartridge recalled?
The products experienced a 12-hour excursion from the required refrigerated temperature conditions at the distribution center prior to distribution.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
lot A1908003
- Product
- Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
- Recalling firm
- Stryker Spine
- Quantity
- 559 total
- Distribution
- US Nationwide Distribution
- Recall date
- July 28, 2021
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)