The Recall Desk

Manufacturer

Ameditech Inc

109 recalls in our database name Ameditech Inc as the manufacturing or recalling firm.

What the numbers show

Total
109
Critical
0
Severe
0
Most recent
2020-10-07

Of the 109 recalls from Ameditech Inc we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

51–75 of 109

  • ModerateFDA (Devices)·Z-0488-2016·2015-12-30

    Ameditech 12-Panel Dip Drug Screen Recalled for Reduced Benzodiazepine Reactivity

    Ameditech is recalling 12-Panel Dip Drug Screen kits because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, 60960D, 61127D, DCC-81205-5, IMCA-10M5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0490-2016·2015-12-30

    Ameditech Benzodiazepine Test Kits Recalled for Reduced Reactivity

    Ameditech Inc is recalling 31,472 Benzodiazepine Strip Dip Card kits because they may show reduced reactivity for Clonazepam and Chlordiazepoxide.

    Product
    BZO Strip Dip Card (300ng/ml)*, Item No. 100170
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0512-2016·2015-12-30

    Ameditech ImmuTest Cup 7-panel Drug Test Recall for Reduced Reactivity

    Ameditech is recalling ImmuTest Cup 7-panel drug tests because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    ImmuTest Cup 7-panel w/ Adulteration, Item No. IMCA-7P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0495-2016·2015-12-30

    Ameditech DrugSmart 12 Test Cup Recall for Reduced Benzodiazepine Reactivity

    Ameditech is recalling DrugSmart 12 Test Cups because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    DrugSmart 12 Test Cup (Multi & BUP), Item No. 61210D DrugSmart 12 Test Cup (Multi/Single/BUP), Item No. 61205D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0541-2016·2015-12-30

    Ameditech 6 Drug Cassette Recall for Reduced Benzodiazepine Reactivity

    Ameditech is recalling 300 kits of the Thermo Fisher 6 Drug Cassette because the tests may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    THERMO FISHER 6 DRUG CASSETTE, Item No. MTPA-6MBAU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0505-2016·2015-12-30

    Ameditech iCup DX 6 Panel Drug Test Recall for Reduced Reactivity

    Ameditech is recalling iCup DX 6 Panel drug tests because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    iCup DX 6 Panel w/Adulterant, Item No. I-DXA-167-013
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0502-2016·2015-12-30

    Ameditech iCup DX 10 Panel Drug Test Recall for Reduced Reactivity

    Ameditech is recalling iCup DX 10 Panel drug tests because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    iCup DX 10 Panel w/Adulterant, Item No. I-DXA-1107-142
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0539-2016·2015-12-30

    Ameditech ProScreen Cup CLIA Drug Test Recall for Reduced Reactivity

    Ameditech is recalling ProScreen Cup CLIA drug tests because they may show reduced reactivity for specific benzodiazepine compounds.

    Product
    ProScreen Cup CLIA with 6 Panel Drug, Item No. PSCup-6MB-W
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0489-2016·2015-12-30

    Ameditech Drugs of Abuse Tests Recalled for Reduced Benzodiazepine Reactivity

    Ameditech is recalling 3,603 kits of 6 Panel Cup Body and Lid w/Adult (AU) because they show reduced reactivity for two specific benzodiazepine compounds.

    Product
    6 Panel Cup Body and Lid w/Adult (AU), Item No. TDDA-6MBAU-CUP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0527-2016·2015-12-30

    Ameditech ProScreen 6 Panel Dip Card Recall for Reduced Benzodiazepine Reactivity

    Ameditech is recalling ProScreen 6 Panel Dip Cards because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    ProScreen 6 Panel Dip Card, Item No. PSCuPSD-6BUP300, PSD-6MTDBO300, PSD-6BUPO, PSD-6MBO, PSD-6MB,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0504-2016·2015-12-30

    Ameditech iCup DX 12 Panel Drug Test Recall for Reduced Reactivity

    Ameditech is recalling iCup DX 12 Panel drug tests because they may show reduced reactivity for two specific benzodiazepine compounds.

    Product
    iCup DX 12 Panel w/ Adulterant, Item No. I-DXA-1127-023
    Category
    Medical Device
    Distribution
    Distributed nationwide