Zimmer Biomet recalls Affixus Hip Fracture Nails with open sterile packaging during surgery. Affected items have lot numbers 584790 or 584810. Consumers should contact the company for details.
There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.
Zimmer Biomet is recalling hip fracture nails that may have open sterile packaging during surgery. This could lead to infection risks if the product is used without proper sterility.
The sterile packaging was found to be open during surgery, which could allow contamination. This poses a risk of infection if the nail is not properly sterilized before use.
Patients who received the Affixus Hip Fracture Nail Left 125 (9 mm x 440 mm) with lot numbers 584790 or 584810. Surgeons and medical staff using these specific items are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 125', size 9 mm x 440 mm, and item number 814409440. Lot numbers 584790 or 584810 indicate affected items.
Reach out to Zimmer Biomet for specific instructions on affected items and next steps.
The recall is due to complaints that the sterile packaging was open during surgery, which could lead to contamination risks.
Contact Zimmer Biomet directly for details on affected items and instructions.
Yes, affected items have lot numbers 584790 or 584810.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0148-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0148-2019 from Zimmer Biomet. 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.