Ameditech Recalls QuickTox 5 Panel Drug Screen DipCard
Ameditech is recalling QuickTox 5 Panel Drug Screen DipCards due to mixed products. The recall affects 3,400 units distributed in 13 US states.
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. The hazard is a product mix-up without reported injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Ameditech Inc is recalling the QuickTox 5 Panel Drug Screen DipCard (Catalog Number QT11, Lot Number 188787). The recall involves 3,400 units, which equates to 136 kits. The product was distributed in Arizona, California, Florida, Georgia, Kansas, Louisiana, Michigan, Missouri, Mississippi, North Carolina, Oklahoma, Tennessee, and Texas.
The recall was initiated because the products were mixed with Alere iScreen Drugs of Abuse Dip Test (P/N X11-IS10-22015-DX, Lot #188744). The source text does not specify the exact nature of the defect or the specific health risks associated with the mixed products, nor does it report any illnesses or injuries.
Users of the affected products should stop using them immediately and contact Ameditech Inc for further instructions or a refund.
The recalled product
- Product
- QuickTox 5 Panel Drug Screen DipCard
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
- 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)
- Catalog Number: QT11 Lot Number: 188787
Distribution
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