FDA recall Z-2779-2020

HF Acquisition Co. LLC · Class II · device

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

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

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