# FDA recall Z-0085-2019

> **Orthosensor, Inc.** · Class II · device recall initiated 2018-07-12.

## Product

OrthoSensor VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, REF ZBH-PSNCRCD39-R.

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** Z-0085-2019
- **Recalling firm:** Orthosensor, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-07-12
- **Report date:** 2018-10-17
- **Termination date:** 2019-06-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Dania, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0085-2019

## Citation

> AI Analytics. FDA recall Z-0085-2019. Retrieved 2026-06-16 from https://api.ai-analytics.org/recall/Z-0085-2019. Source: US FDA. Licensed CC0.

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