Zimmer Biomet recalls LPS FEM IMPLANT SZ H-R devices due to LDPE packaging residue on implants. This may affect patients with severe knee pain needing joint replacement.
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 knee implants that could have LDPE packaging residue on them. This residue might cause issues after surgery, but the recall doesn't specify serious harm or a fix.
The LDPE plastic bag used to package the implants can stick to the implant's surface after removal. This leaves residue that might cause minor issues during healing or future procedures.
Patients who received the LPS FEM IMPLANT SZ H-R knee implants for severe knee pain and disability are likely affected. Those with recent implant procedures may be at slightly higher risk.
Check for the model 'LPS FEM IMPLANT SZ H-R' on the implant or packaging. This device was sold with the part number 00-5996-018-92 between 2010 and 2019.
Look for the model number 'LPS FEM IMPLANT SZ H-R' or part number '00-5996-018-92' on the implant or its packaging.
The recall states there may be LDPE packaging residue on the implant, but it does not mention serious injury or a fix. The risk is considered low.
The recall does not specify a remedy, so no action is required. Check the implant model and part number if you have this device.
The product was sold between 2010 and 2019 based on the part number.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-1034-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1034-2018 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.
