iCup DX 8 Panel w/Adulterant recall
iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016
Why was iCup DX 8 Panel w/Adulterant recalled?
Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity for up to two (2) of the nineteen (19) Benzodiazepine (BZO) compounds for which specificity information is provided in the product insert. The particular BZO compounds for which there may be reduced reactivity are Clonazepam and Chlordiazepoxide.
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?
141971 142195 142397 142674 142997 144209 144463 150018 150883 151525 151526 152180 152741 153045 153150 153151 153211 153376 153650
- Product
- iCup DX 8 Panel w/Adulterant, Item No. I-DXA-187-016
- Recalling firm
- Ameditech Inc
- Quantity
- 8,290 units
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)