Arthrex Suture Washer
Reported: October 12, 2016 Initiated: August 12, 2016 #Z-2918-2016
Product Description
Arthrex Suture Washer
Reason for Recall
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Details
- Recalling Firm
- Arthrex, Inc.
- Units Affected
- 45 devices
- Distribution
- OR, NY, MN, KY, CA, ID, CO, MA, and FL. Thailand.
- Location
- Naples, FL
Frequently Asked Questions
What product was recalled? ▼
Arthrex Suture Washer. Recalled by Arthrex, Inc.. Units affected: 45 devices.
Why was this product recalled? ▼
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 12, 2016. Severity: Low. Recall number: Z-2918-2016.
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