FDA recall record

HF Acquisition Co STAT KIT, Model SM30 recall — FDA Z-2789-2020

Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Class IIclassification
Z-2789-2020official record ID
Aug 19, 2020report date

Recall record at a glance

Official recordZ-2789-2020
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmHF Acquisition Co., LLC
Report dateAug 19, 2020
Recall initiation dateJun 4, 2020
Quantity95 Kits
LocationMukilteo, WA, United States

Official product description

STAT KIT, Model SM30 ; Emergency Medical Kit P/N: 1008670 containing various products to include Narcan Nasal spray, item number 1010300

Why the product was recalled

Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.

Distribution information

U.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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.