Arthrex Fibulock Fibular Nail Instrument Set Reusable recall
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
Why was Arthrex Fibulock Fibular Nail Instrument Set Reusable recalled?
There is a potential for blockage of the Hub Attachment Tube.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Batch/Lot 051838
- Product
- Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide
- Recalling firm
- Arthrex, Inc.
- Quantity
- 47
- Distribution
- Nationwide in US; no distribution OUS.
- Recall date
- February 5, 2020
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)