Ameditech Recalls DrugCheck Pipette 10 Drug Tests Due to Reduced Reactivity
Ameditech is recalling 70 units of DrugCheck Pipette 10 Drug Tests because they have shown reduced reactivity. The affected tests were distributed in the US and Australia.
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 II. The hazard is reduced reactivity, which is a functional defect rather than a direct physical injury or contamination risk, fitting the criteria for a moderate severity recall.
Plain-English summary
Ameditech is recalling 70 units of DrugCheck Pipette 10 Drug Tests, Item No. 41025 DC. These products are one-step immunoassays used for the qualitative detection of multiple drugs and drug metabolites in human urine, including Benzodiazepine (BZO). The tests are intended for professional and point-of-care use.
The recall was initiated because the drug abuse tests have shown reduced reactivity. The affected units were distributed nationwide in the United States and internationally to Australia.
Consumers and healthcare professionals should stop using the affected DrugCheck Pipette 10 Drug Tests and contact Ameditech for further instructions.
The recalled product
- Product
- DrugCheck Pipette 10 Drug Test, Item No. 41025 DC These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, i
- Manufacturer
- Ameditech Inc
- Category
- Medical Device — Diagnostic Test
- Hazard
- Affected units
- 70
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)
- 142512
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 20 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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