Zimmer Biomet recalls VERSYS hip prostheses with LDPE packaging that may leave residue on implants after removal, potentially affecting surgical outcomes. Affected units include specific lot numbers and item codes.
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 VERSYS hip prostheses because the LDPE packaging can leave residue on the implants after removal. This residue might interfere with the implant's function or integration in the body, which could lead to complications after surgery.
The LDPE (low-density polyethylene) packaging material can stick to the highly polished surface of the hip implant. When the implant is removed from the bag, residue from the packaging may remain on the implant, which could affect its performance or integration in the body after surgery.
Patients who received the specific VERSYS hip prosthesis models with the mentioned lot numbers and item codes are affected. Surgeons and medical staff handling these implants during surgery are at higher risk due to potential residue transfer.
Check for the specific item numbers: 00-7843-014-26, 00-7843-014-06, and lot numbers: 61741806, 61886028, 61752736, 62120676. These units were sold with the VERSYS 6-inch beaded FC 14x160mm standard body and neck prosthesis.
Review the item numbers and lot numbers listed in the recall notice to confirm if your prosthesis is affected.
The LDPE packaging may leave residue on the highly polished hip implant after removal, which could affect its function or integration in the body.
Check the item numbers and lot numbers listed in the recall notice to determine if your prosthesis is affected. If affected, contact Zimmer Biomet for further instructions.
The recall indicates a potential issue with implant function, but the hazard is described as low risk as it does not involve immediate danger like injury or death.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1024-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1024-2018 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.
