Ameditech ProScreen 5 Panel Dip Card Recalled for Reduced Benzodiazepine Reactivity
Ameditech is recalling ProScreen 5 Panel Dip Cards because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.
The agency’s classification
FDA (Devices): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
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 III, which is typically a score of 1 or 2. The hazard involves reduced reactivity for specific compounds, which is a performance issue rather than a direct physical injury risk, fitting the Moderate category for low-risk issues.
Plain-English summary
Ameditech Inc is recalling 120 kits of the ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300. 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 product was distributed nationwide.
Consumers should stop using the affected products and contact Ameditech Inc for further instructions.
The recalled product
- Product
- ProScreen 5 Panel Dip Card w/Adult, Item No. PSDA-5MB300
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
- Hazard
- Affected units
- 120
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)
- 152912
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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