Zimmer Biomet recalls a specific lot of PERSONA knee implants due to missing set screw and taper plug in the packaging. This could affect proper installation and safety for patients with severe knee pain.
A complaint was received for Item 42-5320-067-02, lot 63236047. It was report that there was no set screw or taper plug included in the box. Complaint investigation confirmed that the entire lot of 63236047 was missing the set screw and taper plug.
Zimmer Biomet is recalling a specific lot of PERSONA knee implants because the packaging is missing the set screw and taper plug. This could lead to improper installation and potential safety issues for patients needing knee replacements.
The missing set screw and taper plug could prevent proper installation of the knee implant. Without these components, the implant might not function correctly, potentially causing complications during surgery or after use.
Patients who received the PERSONA knee system with lot number 63236047 are affected. Those with severe knee pain from conditions like arthritis are most at risk.
Check the product packaging for lot number 63236047. The PERSONA knee system is indicated for patients with severe knee pain and disability due to conditions like arthritis.
Look for the lot number 63236047 on the packaging of the PERSONA knee system.
The recall is happening because the entire lot 63236047 was reported to be missing the set screw and taper plug, which are necessary for proper installation.
The official notice does not specify a remedy, so contact Zimmer Biomet directly for guidance.
The recall indicates a potential issue with installation, but the official notice does not state that the product is unsafe for 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-1224-2018 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-1224-2018 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.
