# FDA recall Z-0824-2018

> **Trumpf Medical Systems, Inc.** · Class II · device recall initiated 2017-12-15.

## Product

Camera System, Television, Surgical without audio    Intended for transmission and documentation of surgical interventions for the purpose of archiving and teaching.

## Reason for recall

The radiated emission from the TruVidia" Wireless Receiver is above the normative accepted limits, in which the radiated emission may interact with other devices in the operating room and cause them not to function properly.

## Distribution

Worldwide Distribution - US Distribution to the states of : GA, IL, IN, PA, SC, TX, UT, VA.   and to the countries of :  Austria, Australia, Bangladesh, Belgium, France, Switzerland, Czech Republic, Germany, Denmark, Spain, United Arab Emirates, United Kingdom, Ireland, Italy, Kuwait, Lithuania, Poland, Portugal, Romania, Sweden, Slovenia, Thailand, Turkey.

## Key facts

- **Recall number:** Z-0824-2018
- **Recalling firm:** Trumpf Medical Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-15
- **Report date:** 2018-03-07
- **Termination date:** 2020-04-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Charleston, SC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0824-2018

## Citation

> AI Analytics. FDA recall Z-0824-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0824-2018. Source: US FDA. Licensed CC0.

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