ProScreen 6 Panel Cup w/Adult recall
ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU
Why was ProScreen 6 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?
G140258 G140313 G140314 G140368 G140384 G140389 G140399 G140426 G150185 G150199 G150246 G150307
- Product
- ProScreen 6 Panel Cup w/Adult (AU), Item No. PSCupA-6MBAU
- Recalling firm
- Ameditech Inc
- Quantity
- 7,805 kits
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)