Orthosensor recalls VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right 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 E-F/3-11 Right models that have fluid in the posterior lateral corner after surgery. This could lead to complications if not addressed.
The hazard involves fluid accumulation in the posterior lateral corner post-surgery. This could potentially cause complications such as infection or impaired healing if not properly managed.
Patients who received the VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right with specific lot numbers (20569, 20576, 20594, 20618) and UDI 00816818021447 are affected. Those with the recalled model are most at risk.
Check for the VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right model with lot numbers 20569, 20576, 20594, or 20618 and UDI 00816818021447.
Identify if your device has lot numbers 20569, 20576, 20594, or 20618 and UDI 00816818021447.
The recalled device is OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, REF ZBH-PSNCREF311-R.
Lot numbers 20569, 20576, 20594, and 20618 are affected.
The UDI is 00816818021447.
We’ve drafted a message you can send Orthosensor to request your refund or repair — edit it as you like.
Subject: Recall Z-0083-2019 — Orthosensor Orthosensor Hello, I own a Orthosensor that is covered by recall Z-0083-2019 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.
