ProScreen 6 Panel Dip Card recall
ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,
Why was ProScreen 6 Panel Dip Card 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?
141955 142043 142055 142161 142513 142600 142824 142937 142938 142969 143143 143149 143234 143513 143758 143806 143807 144441 152035 152042 152075 152911 153237 153240 153523
- Product
- ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,
- Recalling firm
- Ameditech Inc
- Quantity
- 2,675 kits
- Distribution
- Nationwide Distribution.
- Recall date
- December 30, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)