There is a potential for blockage of the Hub Attachment Tube.
There is a potential for blockage of the Hub Attachment Tube.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Arthrex, Inc. to request your refund or repair — edit it as you like.
Subject: Recall Z-0919-2020 — Arthrex, Inc. Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-steri Hello, I own a Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide that is covered by recall Z-0919-2020 from Arthrex, Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
