Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Reported: December 29, 2021 Initiated: December 3, 2021 #Z-0392-2022
Product Description
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.
Reason for Recall
The incorrect product is contained in the packaging.
Details
- Recalling Firm
- Wright Medical Technology Inc
- Units Affected
- 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.
- Location
- Arlington, TN
Frequently Asked Questions
What product was recalled? ▼
Stryker CLAW II ORTHOLOC 3DSi Plate, Hole Qty: 4, 30mm, REF 40240430.. Recalled by Wright Medical Technology Inc. Units affected: 23 units.
Why was this product recalled? ▼
The incorrect product is contained in the packaging.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 29, 2021. Severity: Moderate. Recall number: Z-0392-2022.
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