Recall Z-0919-2020— Arthrex, Inc.
Class II · Terminated
Class II FDA medical device recall by Arthrex, Inc., initiated 2019-12-17, terminated 2023-08-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide. Reason: There is a potential for blockage of the Hub Attachment Tube..
- Recalling firm
- Arthrex, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-12-17
- Terminated
- 2023-08-31
- Firm location
- Naples, FL, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.