# FDA recall D-0180-2017

> **North American Rescue LLC.** · Class II · drug recall initiated 2016-09-27.

## Product

Amphibious Trauma Kit - Product Code 85-0639,  North American Rescue

## Reason for recall

Lack of Assurance of Sterility: Concerns with product sterility by the manufacturer of the eye wash irrigating solution.

## Distribution

Nationwide, Australia & Switzerland

## Key facts

- **Recall number:** D-0180-2017
- **Recalling firm:** North American Rescue LLC.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2016-09-27
- **Report date:** 2016-12-14
- **Termination date:** 2017-03-09

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0180-2017

## Citation

> AI Analytics. FDA recall D-0180-2017. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-0180-2017. Source: US FDA. Licensed CC0.

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