Home / Recalls / HF Acquisition Co. LLC / Z-2779-2020

Z-2779-2020 Class II Terminated

Recalled by HF Acquisition Co. LLC — Mukilteo, WA

FDA device recall Z-2779-2020 was initiated by HF Acquisition Co. LLC on Jun 5, 2020 and is designated Class II. Reason for recall: A missing component (hand suction pump) in the emergency medical kits. The recall status is terminated (terminated Feb 1, 2022). Affected quantity: 2 kits.

Recall Details

Product Type: Devices
Report Date: Aug 19, 2020
Initiation Date: Jun 5, 2020
Termination Date: Feb 1, 2022
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 2 kits

Product Description

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 Pattern

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

Code Information

STAT KIT Z-1000 Emergency Medical Kit Part Number: 1003550 AMBU Res-Cue Pump part number: 1004330

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2779-2020
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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