RegWardenFDA facility compliance records
Recall

Class II — HF Acquisition Co., LLC

Recalling firmHF ACQUISITION CO. LLC
Registered facilityHF Acquisition Co. LLC (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
ProductSTAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various products to include Narcan Nasal spray, item number 1010300
Quantity155
DistributionU.S. Distribution: CA, FL, NY, AL, WA, CT, OH, MA, TX, NH, WI, ID, MN, DC, IL, MI, PA, MT, AK, NE, MD, CO, GA, VA, WY, MO, HI, SD, AR, TN, KS, ND, WV, NJ, OK, OR, ME, AZ, NC, OUS: None
Initiated2020-06-04
Classified2020-08-12
Terminated2022-07-08
Recall numberZ-2790-2020
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — HF Acquisition Co., LLC (Z-2790-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85911/

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