Home / Recalls / Medical Devices
Orthosensor, Inc. recalls OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
Recalled October 17, 2018 · FDA recall Z-0082-2019 · Orthosensor
Hazard
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery. · FDA Class II
Units
41 devices
Sold at
Distribution was made CA, FL, IL, IN, MI, NY, and NC. Foreign distribution was made to Australia. There was no government/military distribution.
Description
Some sensors were reported to have fluid inside the posterior lateral corner post-surgery.
Product
OrthoSensor VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, REF ZBH-PSNCREF311-L.
Manufacturer(s)
Orthosensor, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →