ProScreen 6 Panel Dip Card w/Adult recall
ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU
Why was ProScreen 6 Panel Dip Card 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?
G150001 G150244 G150293
- Product
- ProScreen 6 Panel Dip Card w/Adult (AU), Item No. PSDA-6MBAU
- Recalling firm
- Ameditech Inc
- Quantity
- 168 kits
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)