Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing Recalled by HF Acquisition Co., LLC Due to Instead of 2 doses, packaged 1 dose of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact HF Acquisition Co., LLC directly.
Affected Products
STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include Narcan Nasal spray, item number 1010300
Quantity: 5
Why Was This Recalled?
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Where Was This Sold?
This product was distributed to 39 states: AL, AK, AZ, AR, CA, CO, CT, FL, GA, HI, ID, IL, KS, ME, MD, MA, MI, MN, MO, MT, NE, NH, NJ, NY, NC, ND, OH, OK, OR, PA, SD, TN, TX, VA, WA, WV, WI, WY, DC
About HF Acquisition Co., LLC
HF Acquisition Co., LLC has 4 total recalls tracked by RecallDetector.
Related Recalls
EndoVive Safety PEG Kit Recalled by Boston Scientific Corporation Due to Recall of kits which utilized ChloraPrep Triple Swabsticks...
Boston Scientific Corporation · February 10, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Artelon FlexBand Dynamic Matrix Ref: 31057 Recalled by International Life Sciences Due to Augmentation devices failed bacterial endotoxin testing.
International Life Sciences · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Owner's Booklets and Instructions for Use that are used with Recalled by Trividia Health, Inc. Due to The system labeling (user manual and online labeling)...
Trividia Health, Inc. · February 6, 2026
Data sourced from the FDA (Device). Last updated March 26, 2026. View original report