FDAClass IIIDecember 30, 2015

ProScreen 10 Panel Cup recall

ProScreen 10 Panel Cup, Item No. PSCup-10M

Why was ProScreen 10 Panel Cup 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?

142596 142984 142985 143144 143145 143146 143240 143241 143351 143875 144102 144106 144239 144241 150651 151706 152165 152167 152168 153102 153107 153251 153411 153412 153633

Product
ProScreen 10 Panel Cup, Item No. PSCup-10M
Recalling firm
Ameditech Inc
Quantity
3,411 kits
Distribution
Nationwide Distribution.
Recall date
December 30, 2015
Classification
Class III
Status
Terminated
Agency
FDA (device)
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