Zimmer Biomet recalls Affixus Hip Fracture Nails with lot number 436650 due to sterile packaging opening during surgery. This could lead to infection risks. Affected users 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 sterile packaging that opens during surgery. This could increase infection risks for patients undergoing the procedure.
The sterile packaging of the hip fracture nail may open during surgery, which could lead to contamination. This increases the risk of infection for the patient if the product is not properly sterilized before use.
Patients who received the Affixus Hip Fracture Nail Left 130 (15 mm x 360 mm) with lot number 436650 during surgery are affected. Surgeons and medical staff using this specific product are at highest risk.
Check for the product name 'Affixus Hip Fracture Nail Left 130' with dimensions 15 mm x 360 mm and item number 814615360. The affected lot number is 436650.
Reach out to Zimmer Biomet directly for specific instructions on how to handle the recalled product.
The recall indicates potential packaging issues during surgery, but the product is generally safe if the packaging remains intact. Affected users should contact Zimmer Biomet for guidance.
If you received the Affixus Hip Fracture Nail Left 130 with lot number 436650, contact Zimmer Biomet for specific instructions.
Check the lot number on the product packaging; affected items have lot number 436650.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0168-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0168-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
