Ameditech ProScreen 8 Panel Dip Card Recalled for Reduced Benzodiazepine Reactivity
Ameditech is recalling ProScreen 8 Panel Dip Cards 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 indicates the product is not likely to cause adverse health consequences, fitting the Moderate severity criteria for minor issues.
Plain-English summary
Ameditech Inc is recalling the ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300. The recall is due to reduced reactivity for up to two of the nineteen Benzodiazepine (BZO) compounds listed in the product insert.
The specific compounds affected by the reduced reactivity are Clonazepam and Chlordiazepoxide. The products were distributed nationwide.
Consumers should stop using the affected products and contact Ameditech Inc for further instructions.
The recalled product
- Product
- ProScreen 8 Panel Dip Card w/Adult, Item No. PSDA-8P, PSDA-8MBO300
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
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)
- 152950 152951 153325
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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