DrugCheck Waived 12 Panel Cup w/Adult recall
DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5
Why was DrugCheck Waived 12 Panel Cup w/Adult 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?
143235 144216 151591 153132 153489
- Product
- DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5
- Recalling firm
- Ameditech Inc
- Quantity
- 1,907 kits
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)