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HF Acquisition Co. LLC

Last updated September 17, 2026

Information

Country: US
Address: 11629 49th Place W, Mukilteo, WA, 98275
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3014534
DUNS Number: —

Catalogue (61)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
Stat Kit Pedi Emergency Medical Kit	1006620	FDA UDI	N	Active
Stat Kit 550 Emergency Medical Kit	STAT KIT 550	FDA UDI	N	Active
Sm Organizer	SM ORGANIZER	FDA UDI	N	Active
SM-Z Emergency Medical Kit	1003420	FDA UDI	N	Active
Sm Organizer	1007760	FDA UDI	N	Unknown
Criti-Kit 200 Emergency Medical Kit	CRITI-KIT 200	FDA UDI	N	Active
Stat Kit Z-1000 Emergency Medical Kit	1003551	FDA UDI	N	Unknown
Stat Kit 550 Emergency Medical Kit (membership)	1009580	FDA UDI	N	Unknown
SM-Z Emergency Medical Kit W/ Nitro Tabs	1003430	FDA UDI	N	Active
Sm7 Select Emergency Medical Kit - Adult	1018350	FDA UDI	N	Unknown
Stat Kit Sm10 Emergency Medical Kit	STAT KIT SM10	FDA UDI	N	Active
Criti-Kit Narcan Opioid Overdose Kit – 2 Doses	Criti-Kit Narcan Opioid Overdose Kit	FDA UDI	N	Unknown
Sm27 Emergency Medical Kit - Adult And Pedi	1003480	FDA UDI	N	Unknown
BIOlogical12	3700	FDA UDI	Class II	Active
Stat Kit 750-Ai Emergency Medical Kit	1006560	FDA UDI	N	Unknown
Mobile Acls V2 Emergency Medical Kit	1003471	FDA UDI	N	Unknown
Faa Emergency Medical Kit Envoy	1007921	FDA UDI	N	Active
Sm-Z Adult Emergency Medical Kit	1003440	FDA UDI	N	Active
Stat Kit 550 Emergency Medical Kit	1006610	FDA UDI	N	Unknown
Stat Kit 750-Ai Emergency Medical Kit	STAT KIT 750-AI	FDA UDI	N	Active
Sm30 Emergency Medical Kit (membership)	1008670	FDA UDI	N	Active
INFLIGHT MEDICAL KIT (Property of American Airlines)	1007101	FDA UDI	N	Active
Mobile Acls Emergency Medical Kit	1003470	FDA UDI	N	Active
Sm30 Emergency Medical Kit	1003510	FDA UDI	N	Unknown
Stat Kit Sm30 Emergency Medical Kit	STAT KIT SM30	FDA UDI	N	Active
Stat Kit 650 Basic Emergency Medical Kit	1006590	FDA UDI	N	Unknown
Sm7 Emergency Medical Kit - Adult	1003490	FDA UDI	N	Unknown
Sm27 Select Emergency Medical Kit	1018330	FDA UDI	N	Unknown
Stat Kit 550-Ai Emergency Medical Kit (membership)	1010830	FDA UDI	N	Unknown
Southwest Eemk Kit	1008001	FDA UDI	N	Active
Mobile Acls V2 Emergency Medical Kit (membership Annual)	1008631	FDA UDI	N	Unknown
Stat Kit 750 Emergency Medical Kit(membership)	1009600	FDA UDI	N	Unknown
SM27 Select Emergency Medical Kit- Adult and Pedi Membership	1018340	FDA UDI	N	Unknown
Stat Kit Sm7 Emergency Medical Kit	STAT KIT SM7	FDA UDI	N	Active
Stat Kit 750 Emergency Medical Kit	1006550	FDA UDI	N	Unknown
Stat Kit 550ai Emergency Medical Kit	1013400	FDA UDI	N	Unknown
Stat Kit 750-R Emergency Medical Kit	1006570	FDA UDI	N	Active
Stat Kit Z-1000 W/ 1 Adult Auto-Injector	1006770	FDA UDI	N	Active
Stat Kit® Z-1000 Emergency Medical Kit (membership)	1009661	FDA UDI	N	Unknown
Stat Kit Pedi-Intubation Emergency Medical Kit	1006630	FDA UDI	N	Active
Sm7 Select Emergency Medical Kit	STAT KIT SM7 SELECT	FDA UDI	N	Active
Stat Kit 750-S Emergency Medical Kit	1006580	FDA UDI	N	Active
Sporetraq Mail-In Spore Testing Service, 12 Tests	1023770	FDA UDI	Class II	Active
Sm10 Emergency Medical Kit (membership)	1008690	FDA UDI	N	Unknown
Inflight Medical Kit Property Of American Airlines V2	1007102	FDA UDI	N	Active
Sm10 Emergency Medical Kit	1003500	FDA UDI	N	Unknown
Stat Kit 750-M Emergency Medical Kit	1006600	FDA UDI	N	Active
Faa Emergency Medical Kit	1006781	FDA UDI	N	Active
Criti-Kit 200-AI	Criti-Kit 200-AI	FDA UDI	N	Active
SM7 Select Emergency Medical Kit- Adult Membership	1018360	FDA UDI	N	Unknown

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Recalls (8)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Apr 13, 2026	Z-2331-2026	—	open, classified	Due to incorrect incubation process being performed on product.
Apr 13, 2026	Z-2332-2026	—	open, classified	Due to incorrect incubation process being performed on product.
Dec 11, 2024	Z-1141-2025	—	open, classified	Spore test strip monitoring system, designed for routine monitoring of sterilization processes, may have a printing error on the return envelope that may cause spore test results to be reported to the incorrect customer's account.
Jun 5, 2020	Z-2779-2020	—	terminated	A missing component (hand suction pump) in the emergency medical kits.
Jun 4, 2020	Z-2789-2020	—	terminated	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Jun 4, 2020	Z-2791-2020	—	terminated	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Jun 4, 2020	Z-2790-2020	—	terminated	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Jun 4, 2020	Z-2788-2020	—	terminated	Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.