HF Acquisition Recalls STAT KIT Emergency Medical Kits with Missing Narcan Dose
HF Acquisition Co., LLC is recalling STAT KIT Model 550AI Emergency Medical Kits because they contain one dose of Narcan Nasal spray instead of two.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text does not report any illnesses, injuries, or hospitalizations. The hazard is a packaging error resulting in a missing dose, which fits the criteria for a moderate severity recall involving low-risk contamination or labeling/packaging issues without reported harm.
Plain-English summary
HF Acquisition Co., LLC is recalling five units of the STAT KIT Model 550AI Emergency Medical Kit, P/N 1010830. The recall is due to a packaging error where the kits contained only one dose of Narcan Nasal spray (item number 1010300) instead of the required two doses.
The affected emergency medical kits were distributed in the following U.S. states and districts: 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, and NC. No international distribution is reported.
Consumers who possess these specific emergency medical kits should stop using them and contact the recalling firm for further instructions. The kits are identified by the product name STAT KIT Model 550AI, P/N 1010830, and contain Narcan Nasal spray item number 1010300.
The recalled product
- Product
- STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include Narcan Nasal spray, item number 1010300
- Manufacturer
- HF Acquisition Co., LLC
- Affected units
- 5
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- STAT KIT¿ 550AI
- Emergency Medical Kit P/N: 1010830 Narcan Nasal spray item number 1010300
Distribution
Part of a larger recall action
This product is one of 4 recalled by HF Acquisition Co., LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
Same manufacturer · HF Acquisition Co., LLC
See all →- ModerateSporeTraq 12-test mail-in spore testing service used incorrect incubation
FDA (Devices) · 2026-06-17
- ModerateSporeTraq 52-test mail-in spore testing service used incorrect incubation
FDA (Devices) · 2026-06-17
- HighSpore Test Monitoring System Printing Error May Cause Result Misdirection
FDA (Devices) · 2025-02-19
- ModerateGlycopyrrolate Injection Vials Recalled Due to Labeling Mix-up
FDA (Drugs) · 2023-06-14
- ModerateHealthFirst STAT KIT Z-1000 Emergency Medical Kits Recalled for Missing Component
FDA (Devices) · 2020-08-19
Same hazard · packaging error
See all →- ModerateTerumo Glidesheath Slender A-Kit Recalled for Incorrect Guidewire Packaging
FDA (Devices) · 2026-08-19
- LowRio II Nasal Pillows Interface Packaging and Labeling Discrepancy Recall
FDA (Devices) · 2026-07-22
- ModerateEMPOWR 3D KNEE insertion instruments recalled for incorrect product size packaging
FDA (Devices) · 2026-07-15
- ModerateArtegraft vascular graft recalled over incorrect lot outer packaging labeling
FDA (Devices) · 2026-03-25
- ModerateBD syringe batch may contain Luer Slip instead of Luer Lok
FDA (Devices) · 2026-03-18