Recall company profile

Ameditech Inc. Recalls

Overview of recall records associated with Ameditech Inc., including dates, categories and classifications where available.

22recall records
Oct 7, 2020latest record date
Oct 7, 2020earliest record date

Recall history in this database

Classification mix: Class II: 22.

Medical DeviceOct 7, 2020

Ameditech Noble 1 Step+ Cup recall — FDA Z-3039-2020

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Class IIFDA: TerminatedAmeditech Inc.
Medical DeviceOct 7, 2020

Ameditech TDDA Drugs of Abuse Cup recall — FDA Z-3044-2020

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Class IIFDA: TerminatedAmeditech Inc.
Medical DeviceOct 7, 2020

Ameditech ToxCup Drug Screen Cup recall — FDA Z-3045-2020

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Class IIFDA: TerminatedAmeditech Inc.
Medical DeviceOct 7, 2020

Ameditech MicroTox recall — FDA Z-3038-2020

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Class IIFDA: TerminatedAmeditech Inc.
Medical DeviceOct 7, 2020

Ameditech MicroScreen recall — FDA Z-3037-2020

Various immunoassay enzymes failed product performance, thereby the products do not consistently detect all calibrator and secondary compounds at the levels stated in the labeling.

Class IIFDA: TerminatedAmeditech Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Ameditech Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.