FDA Device recall Z-2788-2020
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150
- FDA Device
- Class II
- terminated
- Published 2020-08-19
On 2020-08-19 the FDA classified a Class II recall of HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150 by Hf Acquisition, citing instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2788-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-04 |
| Published | 2020-08-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hf Acquisition |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, ID, IL, KS, MA, MD, ME, MI, MN, MO, MT, NC, ND, NE, NH, NJ, NY, OH, OK, OR, PA, SD, TN, TX, VA, WA, WI, WV, WY |
Product
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place West/Mukilteo, WA 98275, HealthFirst.com; Store at Room Temperature. 9036-2v.5 08/2017 containing various products to include Narcan Nasal spray, item number 1010300
Reason
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Identifiers
| code_info | SM7 (NARCAN Upgrade Bundle): P/N: 1008150 SM7 Emergency Medical Kit |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2788-2020%22
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