HealthFirst STAT KIT Z-1000 Emergency Medical Kits Recalled for Missing Component
HF Acquisition Co. LLC is recalling two STAT KIT Z-1000 emergency medical kits because they are missing a hand suction pump component.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard is a missing component in a medical kit, which is a functional defect but does not involve a high-risk pathogen, structural vehicle defect, or reported injuries, fitting the Moderate criteria for low-risk contamination or functional issues without reported harm.
Plain-English summary
HF Acquisition Co. LLC is recalling two units of the STAT KIT Z-1000 emergency medical kit. The recall is due to a missing component, specifically a hand suction pump, in the emergency medical kits.
The affected kits are intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives. The distribution was nationwide in the US, including the states of Tennessee and Utah.
The specific part numbers involved are 1003550 for the STAT KIT Z-1000 Emergency Medical Kit and 1004330 for the AMBU Res-Cue Pump. Consumers should check their kits for the presence of the hand suction pump and contact the recalling firm if the component is missing.
The recalled product
- 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.
- Manufacturer
- HF Acquisition Co. LLC
- Hazard
- Affected units
- 2
Distribution
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