Zimmer Biomet recalls VERSYS hip implants due to LDPE packaging residue that may remain on implants after removal. Affected units have specific model 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 hip prostheses because packaging material may leave residue on the implants after removal. This could affect the implant's performance or longevity, but the risk is not severe enough to require immediate discontinuation.
The LDPE bag packaging may stick to the highly polished surface of the implant, leaving residue after the implant is removed from the bag. This residue could potentially affect the implant's performance or longevity.
Patients who received the specific VERSYS hip prosthesis model with lot number 62158840 are affected. Those with the implant are most at risk.
Check for the model name 'VERSYS 7.5 INCH BEADED FC REV 13.5X190MM STRAIGHT' and lot number 62158840 on the implant packaging or documentation.
Reach out to Zimmer Biomet directly for specific instructions on whether your implant is affected and next steps.
The recall indicates a potential for packaging residue on the implant, but the hazard is not severe enough to cause serious injury or immediate action.
Check for the model name 'VERSYS 7.5 INCH BEADED FC REV 13.5X190MM STRAIGHT' and lot number 62158840 on the implant packaging or documentation.
Contact Zimmer Biomet directly for specific instructions on whether your implant is affected and next steps.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1028-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1028-2018 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.
