12-Panel Dip Drug Screen with adulterant recall
12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of…
Why was 12-Panel Dip Drug Screen with adulterant recalled?
Ameditech is recalling drug abuse tests because they have shown reduced reactivity.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
144302 150323 150661 151143 151467
- Product
- 12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of…
- Recalling firm
- Ameditech Inc
- Quantity
- 960 units
- Distribution
- Worldwide Distribution - US (nationwide) and Internationally to Australia.
- Recall date
- November 25, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)