Zimmer Biomet recalls VERSYS hip prosthesis models with LDPE packaging that may leave residue on implants after removal. Affected units include specific sizes and lot numbers. Consumers should contact the company for details.
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 prosthesis models because the LDPE packaging may leave residue on the implants after removal. This could affect the implant's performance and long-term success.
The LDPE bag packaging may adhere to the highly polished surface of the hip implant, leaving residue or material on the implant after it is removed from the bag. This residue could potentially affect the implant's performance and long-term success.
Patients who received the recalled VERSYS hip prosthesis models with specific sizes and lot numbers are affected. Those with implants made from the listed item numbers and lot numbers are most at risk.
Check the item number and lot number on the packaging. Affected models include VERSYS 6 INCH BEADED FC STEM with sizes 12X160MM, 13X160MM, 15X160MM, and 17X160MM LM Prosthesis, Hip, Semi-Constrained.
Reach out to Zimmer Biomet directly for specific details about your implant model and lot number.
The recall is for potential residue from packaging on the implant, which could affect long-term performance but is not immediately hazardous.
The affected models include VERSYS 6 INCH BEADED FC STEM with sizes 12X160MM, 13X160MM, 15X160MM, and 17X160MM LM Prosthesis, Hip, Semi-Constrained.
Check the item number and lot number on the packaging. Affected units have specific item numbers and lot numbers listed in the recall notice.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1026-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1026-2018 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.
