Zimmer Biomet recalls hip prostheses with LDPE packaging that may leave residue on implants after removal, risking contamination. Affected models include VERSYS 7.5-inch beaded FC implants with specific lot numbers.
The LDPE bag packaging for various highly polished hip and knee implants may adhere to the highly polished surface, leaving residue or material from the LDPE bag on the implant after it is removed from the bag.
Zimmer Biomet is recalling certain hip prostheses due to LDPE packaging residue that may remain on the implant after removal. This residue could potentially cause contamination or complications during surgery.
The LDPE (low-density polyethylene) packaging material may adhere to the highly polished surface of the hip implant after it is removed from the bag. This residue could potentially contaminate the implant during surgery or cause complications if not properly cleaned.
Patients who received the recalled hip prostheses with specific lot numbers and item numbers from the list provided. Surgeons and medical staff handling these implants during surgery are at higher risk due to potential contamination.
Check the item number and lot numbers listed in the recall notice. Affected models include VERSYS 7.5-inch beaded FC hip prostheses with specific lot numbers such as 61946025, 61735805, and others.
Review the item number and lot numbers provided in the recall notice to determine if your prosthesis is affected.
The LDPE packaging may leave residue on the highly polished implant surface after removal, potentially causing contamination during surgery.
Check the item number and lot numbers listed in the recall notice to determine if your prosthesis is affected. Contact Zimmer Biomet for further instructions.
The recall addresses potential contamination during surgery, but the hazard is considered low risk as it does not involve immediate danger to the patient in normal use.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1027-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1027-2018 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.
