Orthosensor, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0086-2019)

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 G-H/7-12 Left, REF ZBH-PSNCRGH712-L.

Product Classification:

Class II

Date Initiated: July 12, 2018

Date Posted: October 17, 2018

Recall Number: Z-0086-2019

Event ID: 80845

Reason for Recall:

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

Status: Terminated

Product Quantity: 84 devices

Code Information:

Lot numbers 20549, 20565, 20606, 20610, 20615, UDI 00816818021454.

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