Zimmer Biomet recalls Affixus Hip Fracture Nails with open sterile packaging during surgery. Affected items have lot number 500220. 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 or contamination if used without proper sterilization.
The sterile packaging may be open when the product is opened in surgery. This could mean the nail is not properly sterilized, increasing the risk of infection or contamination during the procedure.
Patients who received the Affixus Hip Fracture Nail Left 130 (11 mm x 400 mm) with lot number 500220 during surgery. Surgeons and medical staff using the product are most at risk.
Check for the product name 'Affixus Hip Fracture Nail Left 130', size 11 mm x 400 mm, and lot number 500220. The product is used for hip fracture fixation.
Reach out to Zimmer Biomet for specific instructions on how to handle the recalled item.
The recall indicates potential open sterile packaging during surgery, which could lead to contamination. The product is not safe for use as recalled.
Contact Zimmer Biomet directly for instructions on handling the recalled item.
Look for the product name 'Affixus Hip Fracture Nail Left 130', size 11 mm x 400 mm, and lot number 500220.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-0167-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-0167-2019 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.