HF Acquisition Recalls Emergency Medical Kits with Missing Narcan Dose
HF Acquisition Co., LLC is recalling 95 STAT KIT Model SM30 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 minor labeling/packaging errors without reported harm.
Plain-English summary
HF Acquisition Co., LLC is recalling 95 units of the STAT KIT, Model SM30 (Emergency Medical Kit P/N: 1008670). The recall is due to a packaging error where the kits contain one dose of Narcan Nasal spray (item number 1010300) instead of the required two doses.
The affected kits were distributed across 39 U.S. states and the District of Columbia, including California, Florida, New York, and Texas. No international distribution is reported.
Consumers who possess these kits should stop using them and contact the recalling firm for instructions on return or replacement. The kits are intended for emergency medical use, and the missing dose may impact the ability to administer the full prescribed treatment.
The recalled product
- Product
- STAT KIT, Model SM30 ; Emergency Medical Kit P/N: 1008670 containing various products to include Narcan Nasal spray, item number 1010300
- Manufacturer
- HF Acquisition Co., LLC
- Affected units
- 95
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 (3)
- STAT KIT¿ SM30
- Emergency Medical Kit P/N: 1008670 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.
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