HF Acquisition Co LLC

FDA Regulatory Profile

HF Acquisition Co LLC has 10 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest recall
Z-2332-2026 · Class II · Apr 13, 2026
Latest inspection
Jun 26, 2025 · VAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls10Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
Z-2332-2026Class IIBrand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE…Apr 13, 2026
Z-2331-2026Class IIBrand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE…Apr 13, 2026
Z-1141-2025Class IIBiological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12…Dec 11, 2024
D-0870-2023Class IIIGLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo…Jun 6, 2023
D-1392-2020Class IIIFamotidine Injection, USP, 20 mg/2mL, 2 mL vial, Rx only, Single Dose Vial, For Intravenous Use Only…Jun 17, 2020
Z-2779-2020Class IISTAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians…Jun 5, 2020
Z-2791-2020Class IISTAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include…Jun 4, 2020
Z-2789-2020Class IISTAT KIT, Model SM30 ; Emergency Medical Kit P/N: 1008670 containing various products to include…Jun 4, 2020
Z-2788-2020Class IIHealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC…Jun 4, 2020
Z-2790-2020Class IISTAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various products to include Narcan…Jun 4, 2020

Recent FDA Inspections

DateSiteProductClassificationFEI
Jun 26, 2025Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Oct 10, 2019Mukilteo, WADrugsNo Action Indicated (NAI)3014534
Feb 9, 2018Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Nov 5, 2014Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Oct 29, 2013Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Oct 13, 2011Mukilteo, WADrugsNo Action Indicated (NAI)3014534
Nov 30, 2010Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Jan 19, 2010Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534
Dec 10, 2008Mukilteo, WADrugsVoluntary Action Indicated (VAI)3014534

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3014534Mukilteo, WA9Jun 26, 2025

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.