Ameditech ProScreen 9 Panel Cup Recall for Reduced Benzodiazepine Reactivity
Ameditech is recalling ProScreen 9 Panel Cup kits because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The agency classification is Class III, which the rubric defines as unlikely to cause adverse health consequences, typically resulting in a score of 1 or 2.
Plain-English summary
Ameditech Inc is recalling 3 kits of the ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300. The product was 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 affected are Clonazepam and Chlordiazepoxide.
The source text does not specify instructions for consumers or the number of affected units beyond the 3 kits listed in the structured data.
The recalled product
- Product
- ProScreen 9 Panel Cup w/Adulterants, Item No. PSCUPA-9BO300
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
- Hazard
- Affected units
- 3
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)
- G150252
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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