Zimmer Biomet recalls XP-XP Tibial Tray Interlok 59mm (Item #195750) due to locking bar not fully engaging, which could lead to improper joint alignment during surgery.
The locking bar not fully engaging
Zimmer Biomet is recalling XP-XP Tibial Tray Interlok 59mm implants (Item #195750) because the locking bar may not engage properly during surgery. This could cause improper joint alignment and potentially lead to complications for patients needing joint replacement.
The locking bar may not fully engage during surgery, which could result in improper alignment of the joint. This might cause complications such as misalignment or instability in the joint after surgery.
Patients who have received the XP-XP Tibial Tray Interlok 59mm implant (Item #195750) from Zimmer Biomet are affected. Surgeons and medical staff who use this implant during joint replacement procedures are at risk.
Check for the product name 'XP-XP Tibial Tray - Interlok 59 mm' and the item number 195750. The lot numbers listed (206540, 057180, etc.) indicate specific batches that are affected.
Identify the item number and lot numbers listed in the recall notice to confirm if your implant is affected.
The recall states the locking bar may not fully engage, which could lead to improper joint alignment during surgery. However, the specific risk level is not clearly described in the notice.
The recall does not specify a remedy, so you should check the product details to see if your implant is affected and contact Zimmer Biomet for further instructions.
Look for the product name 'XP-XP Tibial Tray - Interlok 59 mm' and the item number 195750. The affected lot numbers are 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-2527-2019 — Zimmer Biomet Zimmer Biomet Hello, I own a Zimmer Biomet that is covered by recall Z-2527-2019 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.
