Orthosensor, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0082-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: July 12, 2018

Date Posted: October 17, 2018

Recall Number: Z-0082-2019

Event ID: 80845

Reason for Recall:

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

Status: Terminated

Product Quantity: 41 devices

Code Information:

Lot numbers 20568, 20575, 20581, 20584, 20621, 20623, and 20628, UDI 00816818021430.

Distribution Pattern:

Distribution was made CA, FL, IL, IN, MI, NY, and NC. Foreign distribution was made to Australia. There was no government/military distribution.

Voluntary or Mandated:

Voluntary: Firm initiated