# FDA recall Z-2779-2020

> **HF Acquisition Co. LLC** · Class II · device recall initiated 2020-06-05.

## Product

STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives.

## Reason for recall

A missing component (hand suction pump) in the emergency medical kits.

## Distribution

US Nationwide distribution including in the states of TN and UT.

## Key facts

- **Recall number:** Z-2779-2020
- **Recalling firm:** HF Acquisition Co. LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-05
- **Report date:** 2020-08-19
- **Termination date:** 2022-02-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mukilteo, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2779-2020

## Citation

> AI Analytics. FDA recall Z-2779-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2779-2020. Source: US FDA. Licensed CC0.

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