# FDA recall Z-1681-2019

> **King Systems Corp. dba Ambu, Inc.** · Class II · device recall initiated 2019-01-04.

## Product

King LTS-D Kit Size 1, Model Number KLTSD431

## Reason for recall

Size 0 products were incorrectly packaged and labeled as a size 1 products.

## Distribution

The products were distributed to the following US states:  CA, CT, FL, IA, IN, MD, MS, NC, PA, TX, and WI.

## Key facts

- **Recall number:** Z-1681-2019
- **Recalling firm:** King Systems Corp. dba Ambu, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-04
- **Report date:** 2019-06-05
- **Termination date:** 2020-04-20

- **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-1681-2019

## Citation

> AI Analytics. FDA recall Z-1681-2019. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1681-2019. Source: US FDA. Licensed CC0.

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