Z-2790-2020 Class II Terminated

Recalled by HF Acquisition Co., LLC — Mukilteo, WA

FDA device recall Z-2790-2020 was initiated by HF Acquisition Co., LLC on Jun 4, 2020 and is designated Class II. Reason for recall: Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. The recall status is terminated (terminated Jul 8, 2022). Affected quantity: 155.

Recall Details

Product Type
Devices
Report Date
Aug 19, 2020
Initiation Date
Jun 4, 2020
Termination Date
Jul 8, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
155

Product Description

STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various products to include Narcan Nasal spray, item number 1010300

Reason for Recall

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

Distribution Pattern

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

Code Information

STAT KIT¿ 550 ; Emergency Medical Kit P/N: 1009580 Narcan Nasal spray, item number 1010300

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-2790-2020
openFDA file date
Nov 10, 2026
Loaded by RegDataLab
Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

Source: openFDA record for Z-2790-2020. Report a data issue: hello@regdatalab.com.