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Recall Observatory FDA recall evidence

Device product

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

Z-0086-2019

July 12, 2018

Class II

Product summary

Firm
Orthosensor, Inc.
Event
Event 80845
Status
Terminated
Classification
Class II
Quantity
84 devices
Official record key
device-enforcement:Z-0086-2019

Official wording

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

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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