Ameditech Inc: Medical Device Recall in 2018 - (Recall #: Z-0270-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup is an in vitro diagnostic test for the rapid detection of multiple drugs in human urine. The test is intended as the first step in a two-step process to provide consumers with information concerning the presence or absence of drugs or their metabolites in a urine sample. Information regarding confirmatory testing- the second step in the process-is provided in the package labeling.

Product Classification:

Class III

Date Initiated: September 30, 2017

Date Posted: October 31, 2018

Recall Number: Z-0270-2019

Event ID: 80861

Reason for Recall:

Product was released to market without the adulteration strip included in the product.

Status: Terminated

Product Quantity: 40 kit boxes (1000 units)

Code Information:

Part Number: DS84S625, Lot Number: 174886 (US distribution only)

Distribution Pattern:

US in the state of California

Voluntary or Mandated:

Voluntary: Firm initiated