Zimmer Biomet recalls Affixus Hip Fracture Nails with set screw that cannot advance or reverse. This may cause improper fixation during hip fracture surgery. Affected items have specific model and item numbers.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling hip fracture nails that have a set screw which won't move properly. This could lead to improper bone fixation during surgery, risking complications for patients needing hip fracture repair.
The set screw in the nail cannot advance or reverse from its original position. This means the nail may not hold securely in the bone during hip fracture surgery, potentially causing improper fixation and complications.
Patients who received the Affixus Hip Fracture Nail Right 130 model (15 mm x 440 mm) with item number 814515440 from the manufacturer. Surgeons and medical staff using this specific nail during hip fracture procedures are most at risk.
Check for the Affixus Hip Fracture Nail Right 130 model (15 mm x 440 mm) with item number 814515440. This product was sold under the manufacturer's name Zimmer Biomet.
Verify the model number and item number on the product to confirm if it matches the recalled Affixus Hip Fracture Nail Right 130 (15 mm x 440 mm) with item number 814515440.
The recall states the set screw may not advance or reverse, which could lead to improper bone fixation during hip fracture surgery. However, the remedy is not specified, so the risk level is low.
The recall record does not specify a remedy, so there is no action required beyond checking if your product matches the recalled model.
Check for the Affixus Hip Fracture Nail Right 130 model (15 mm x 440 mm) with item number 814515440 on the product label or packaging.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3145-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3145-2018 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.
