Reported Nov 25, 2015 · Terminated

ProScreen 10 Drug Panel Cassette Test, Item No. CPSP-10PPX; ProScreen 10 Panel Cup, Item No. PSCup-10MMO-300,…

Ameditech Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Ameditech Inc · 9940 Mesa Rim Rd · San Diego, CA · 92121-2910

Is this the product you have?

23 of 23 products

Products covered by this recall
Model / numberProduct as published
CPSP-10PPXProScreen 10 Drug Panel Cassette Test
PSCup-10MMO-300ProScreen 10 Panel Cup, , PSCup-10M, PSCupA-10MO, PSCUp-10AB
PSCupA-10AMProScreen 10 Panel Cup with Adulterants
PSD-10MMO-300ProScreen 10 Panel Dip Card, , PSD-10MOX, PSD-10M, PSD-10CMO3, PSD-10APO-300
PSDA-10MOProScreen 10 Panel Dip Card w/Adult, , PSDA-10MMO-300
PSD-11MTProScreen 11 Panel Dip Card
PSCupA-12TBUProScreen 12 Drug Cup w/Adulteration
PSCupA-12MProScreen 12 Panel Cup w/Adult., , PSCupA-12PP
PSD-5MBProScreen 12 Panel Dip Card, Item No. PSD-12BUP ProScreen 5 Panel Dip Card
PSDA-5MB-300ProScreen 5 Panel Dip Card w/Adult
PSPA-6MBAUProScreen 6 Panel Cassette w/Adult (AU)
PSCupA-6MBAUProScreen 6 Panel Cup w/Adult (AU)
PSD-6MBOProScreen 6 Panel Dip Card, , PSD-6MTDBO-300, PSD-6MB, PSD-6BUPO
PSD-7MOProScreen 7 Panel Dip Card, , PSD-7M
PSD-8PProScreen 8 Panel Dip Card
PSDA-8PProScreen 8 Panel Dip Card w/Adult
PSD-9PProScreen 9 Panel Dip Card
PSCupA-6MB-WProScreen CLIA Waived Cup 6 Drugs w/Adul
PSCup-6BO-WProScreen CLIA Waived Cup with 6 Drugs
PSCup-8P-WProScreen CLIA Waived Cup with 8 Drug
Lot codes and dates
  • 183 of 183 codes

    • 134545
    • 150270
    • 150542
    • 134346
    • 134347
    • 141739
    • 141836
    • 141841
    • 142565
    • 142951
    • 143151
    • 143875
    • 144102
    • 144106
    • 144239
    • 144241
    • 144362
    • 150192
    • 150198
    • 150629
    • 150630
    • 150651
    • 150791
    • 150959
    • 151037
    • 151358
    • 151359
    • 143402
    • 143813
    • 144240
    • 151395
    • 134181
    • 141028
    • 141458
    • 142039
    • 142111
    • 142385
    • 142396
    • 142498
    • 142717
    • 142823
    • 142957
    • 142972
    • 143514
    • 143828
    • 144298
    • 144301
    • 144308
    • 144309
    • 144310
    • 144519
    • 144520
    • 144540
    • 144541
    • 150087
    • 150108
    • 150145
    • 150169
    • 150514
    • 150516
Amount recalled
31,530 units

This recall covers 20 products

The agency filed one notice per product. You are reading one of them; the other 19 are below.

7 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Ameditech is recalling drug abuse tests because they have shown reduced reactivity.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 9, 2016 · Data as of Sep 19, 6:03 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.