Ameditech DrugSmart 11 Test Cup Recalled for Reduced Benzodiazepine Reactivity
Ameditech is recalling DrugSmart 11 Test Cups because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.
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 III, which is defined as unlikely to cause adverse health consequences. The issue involves reduced reactivity for specific compounds, which is a performance defect rather than a direct physical hazard like injury or death.
Plain-English summary
Ameditech Inc is recalling 320 kits of the DrugSmart 11 Test Cup, Item No. 61127D. The affected products were distributed nationwide.
The recall was initiated because the drugs of abuse tests have shown reduced reactivity for up to two of the nineteen Benzodiazepine (BZO) compounds listed in the product insert. The specific compounds with potential reduced reactivity are Clonazepam and Chlordiazepoxide.
Consumers should check their DrugSmart 11 Test Cups for the following lot codes: 144196, 144375, 150096, 151980, or 152737. If the product matches these codes, users should stop using it and contact Ameditech Inc for instructions.
The recalled product
- Product
- DrugSmart 11 Test Cup, Item No. 61127D
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
- Affected units
- 320
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)
- 144196 144375 150096 151980 152737
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 59 recalled by Ameditech Inc 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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