medical Class II Updated 2018-10-17

Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11

Recalled Product

OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, REF ZBH-PSNCREF311-R.


Hazard / Issue

Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.

Issued by

FDA

Affected States: CA, FL, IL, IN, MI, NY, NC
Lot/Code Info: Lot numbers 20569, 20576, 20594, and 20618, UDI 00816818021447.
View official government recall

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