Orthosensor recalls VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right with fluid in posterior lateral corner post-surgery. Affected units have lot numbers 20598 and 20607.
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Orthosensor is recalling specific VERASENSE models for Zimmer Biomet Persona CR C-D/3-9 Right implants due to reported fluid in the posterior lateral corner after surgery. This could lead to complications if not addressed.
The recall reports fluid in the posterior lateral corner post-surgery. This could cause complications such as infection or improper healing if the fluid is not managed correctly.
Patients who received the VERASENSE implant with lot numbers 20598 or 20607 are affected. Those with the specific UDI code 00816818021423 are at risk.
Check for lot numbers 20598 or 20607 on the VERASENSE implant. The unique device identifier (UDI) 00816818021423 also identifies affected units.
Look for lot numbers 20598 or 20607 and UDI 00816818021423 on the VERASENSE implant.
The recall reports fluid in the posterior lateral corner post-surgery, which could lead to complications.
Check the implant for lot numbers 20598 or 20607 and UDI 00816818021423. Contact Orthosensor for further instructions.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Orthosensor to request your refund or repair — edit it as you like.
Subject: Recall Z-0085-2019 — Orthosensor Orthosensor Hello, I own a Orthosensor that is covered by recall Z-0085-2019 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.
