Accutest Drug Test Cup 5+3 Product Usage: The Accutest Drug Test Cup… — Class III medical device recall Z-0270-2019
Terminated recall by Ameditech Inc, reported 2018-10-31, distributed in CA. Product was released to market without the adulteration strip included in the product.
| Recall number | Z-0270-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Ameditech Inc, San Diego, CA, United States |
| Recall initiated | 2017-09-30 |
| Classified | 2018-10-25 |
| Reported by FDA | 2018-10-31 |
| Terminated | 2019-08-06 |
| Distributed | CA |
| Lot numbers | 174886 |
| Model numbers | DS84S625 |
Product
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.
Reason for recall
Product was released to market without the adulteration strip included in the product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0270-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.