Zimmer Biomet recalls XP-XP Tibial Tray - Interlok 73mm (Item #195756) due to locking bar not fully engaging, which may cause improper alignment during surgery. Affected units have specific lot numbers.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-XP Tibial Tray - Interlok 73mm (Item #195756) because the locking bar might not engage properly during surgery. This could lead to incorrect bone alignment and potential complications for patients.
The locking bar may not fully engage during surgical procedures, which could result in improper alignment of the bone. This might cause complications such as misshapen bones or unstable joint structures after surgery.
Orthopedic surgeons and medical facilities that use this specific surgical implant are likely affected. Patients who have received this implant during surgery are at risk of improper bone alignment.
Check for the product name 'XP-XP Tibial Tray - Interlok 73mm' with Item #195756. Affected units have specific lot numbers listed in the recall notice.
Reach out to Zimmer Biomet directly to confirm if your implant is affected and get instructions for next steps.
This recall applies to the XP-XP Tibial Tray - Interlok 73mm (Item #195756) used during surgery. If you received this specific implant, contact Zimmer Biomet for guidance.
Check the product name and lot numbers listed in the recall notice. Affected units have specific lot numbers including 562200, 664340, and others as detailed in the record.
Contact Zimmer Biomet directly to confirm if your implant is affected and get instructions for next steps. The recall does not include a specific remedy.
We’ve drafted a message you can send Zimmer Biomet to request your refund or repair — edit it as you like.
Subject: Recall Z-2521-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2521-2019 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.
