Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Reported: February 5, 2020 Initiated: December 17, 2019 #Z-0919-2020
Product Description
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Reason for Recall
There is a potential for blockage of the Hub Attachment Tube.
Details
- Recalling Firm
- Arthrex, Inc.
- Units Affected
- 47
- Distribution
- Nationwide in US; no distribution OUS.
- Location
- Naples, FL
Frequently Asked Questions
What product was recalled? ▼
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide. Recalled by Arthrex, Inc.. Units affected: 47.
Why was this product recalled? ▼
There is a potential for blockage of the Hub Attachment Tube.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 5, 2020. Severity: Moderate. Recall number: Z-0919-2020.
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