Stryker CLAW II ORTHOLOC 3DSi Plate recall
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Why was Stryker CLAW II ORTHOLOC 3DSi Plate recalled?
The incorrect product is contained in the packaging.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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 #1642103
- Product
- Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
- Recalling firm
- Wright Medical Technology Inc
- Quantity
- 23 units
- Distribution
- Worldwide distribution in the states of AZ, IA, ID, NC, NY, VA, and WV. The countries of Canada, France, Germany, Lebanon, The Netherlands, Saudi Arabia, and United Kingdom.
- Recall date
- December 29, 2021
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)