Medi-First First Aid Kits Recalled Due to Stability Testing Failures
Total Resources International is voluntarily recalling Medi-First 61 Piece First Aid Kits because Benzalkonium Chloride failed stability testing.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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 and is a voluntary precautionary recall due to stability testing failures, with no reported injuries or illnesses.
Plain-English summary
Total Resources International is voluntarily recalling Medi-First Brand First Aid Kits, specifically the 61 Piece Kit. The recall is being initiated due to failures in stability testing of the active ingredient Benzalkonium Chloride.
The affected products are identified by Lot 11214-07. The recall is classified as Class II by the U.S. Food and Drug Administration.
Consumers who have this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Medi-First Brand First Aid Kit, MEDI-FIRST 61 Piece Kit, Home, Workplace Travel, Sport, Total Resources International, Walnut, CA 91789
- Manufacturer
- Total Resources Intl
- Category
- Drug — First Aid Kits
- Hazard
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 (1)
- Lot 11214-07
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Total Resources Intl under a single FDA (Drugs) 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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