Zimmer Biomet recalls Affixus Hip Fracture Nail Left 130 (11mm x 460mm) due to set screw not advancing or reversing properly. Affected units may need replacement.
The set screw is not able to advance or reverse from the original position in the nail.
Zimmer Biomet is recalling Affix:us Hip Fracture Nails Left 130 (11mm x 460mm) because the set screw can't move properly. This could lead to improper fixation during hip fracture surgery, risking complications for patients.
The set screw in the nail cannot advance or reverse from its original position. This means the nail may not stay securely in place during surgery, potentially causing improper healing or complications after the procedure.
Patients who received this specific hip fracture nail implant during surgery are affected. Surgeons and medical teams using the product are most at risk of improper application.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 460 mm. The item number 814611460 is also associated with this recall.
Reach out to Zimmer Biomet directly for guidance on the recall and potential replacement options.
The recall indicates the set screw may not function properly, which could lead to improper fixation during hip fracture surgery. However, the specific risk level is not detailed in the official notice.
Look for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 11 mm x 460 mm and item number 814611460.
The official recall does not specify a stop-use instruction, so immediate action is not required. Contact Zimmer Biomet for further guidance.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-3162-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-3162-2018 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.
