# FDA recall Z-0916-2020

> **King Systems Corp. dba Ambu, Inc.** · Class I · device recall initiated 2019-11-05.

## Product

King Vision Video Adapter Size 1/2.  Laryngoscope used to examine and visualize a patients upper airway and aid in the placement of a tracheal tube.  Model Number: KVLVA12

## Reason for recall

Exhibiting a reversed image. Although the image may appear normal, the users actions will be reversed on the display for left and right  directions.

## Distribution

Worldwide distribution.  US Nationwide, Australia, Belgium, Bolivia, Canada,  Costa Rica, Germany, Hong Kong, India, Italy, Japan, Myanmar, Poland, Spain, and UK.

## Key facts

- **Recall number:** Z-0916-2020
- **Recalling firm:** King Systems Corp. dba Ambu, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-11-05
- **Report date:** 2020-02-12
- **Termination date:** 2021-03-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Noblesville, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0916-2020

## Citation

> AI Analytics. FDA recall Z-0916-2020. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0916-2020. Source: US FDA. Licensed CC0.

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