medical Class II Updated 2018-10-17

Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12

Recalled Product

OrthoSensor VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left, REF ZBH-PSNCRGH712-L.


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 20549, 20565, 20606, 20610, 20615, UDI 00816818021454.
View official government recall

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