Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-s
See all recalls from Arthrex, Inc. →Recalled Product
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Hazard / Issue
There is a potential for blockage of the Hub Attachment Tube.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Batch/Lot 051838
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Arthrex Fibulock Fibular Nail →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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