Orthosensor recalls VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left with fluid in posterior lateral corner post-surgery. Affected units have specific lot numbers and UDI.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Orthosensor is recalling VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left implants due to reported fluid in the posterior lateral corner after surgery. This could affect surgical outcomes and requires attention from users.
The hazard involves fluid accumulation in the posterior lateral corner area after surgery, which may lead to complications. This issue was reported by users but has not been confirmed to cause serious injury in normal use.
Patients who received the VERASENSE implant for Zimmer Biomet Persona CR G-H/7-12 Left with lot numbers 20549, 20565, 20606, 20610, 20615, or UDI 00816818021454 are most at risk. Medical professionals using these implants should also check.
Check for the VERASENSE implant model: Zimmer Biomet Persona CR G-H/7-12 Left. Look for lot numbers 20549, 20565, 20606, 20610, 20615, or UDI 00816818021454.
Review the lot number and UDI on your VERASENSE implant to confirm if it is affected.
The recall reports fluid in the posterior lateral corner post-surgery, but it has not been confirmed to cause serious injury. The official notice does not specify a risk level.
Check your implant's lot number and UDI to see if it matches the affected units listed. The recall does not provide a specific remedy.
Look for lot numbers 20549, 20565, 20606, 20610, 20615, or UDI 00816818021454 on your VERASENSE implant for Zimmer Biomet Persona CR G-H/7-12 Left.
We’ve drafted a message you can send Orthosensor to request your refund or repair — edit it as you like.
Subject: Recall Z-0086-2019 — Orthosensor Orthosensor Hello, I own a Orthosensor that is covered by recall Z-0086-2019 from Orthosensor. 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.
