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eScreen eReader V3Recalls & reported problems

Escreen, Inc. · The eScreen eReader is a sophisticated appliance that uses digital technology to scan the test lid of a sealed eCup, providing an automated, objective, confidential testing process. The eReader uses bar code technology, coupled with optical imaging, to electronically capture the drug test results from eCups without the subjectivity of a clinician reading them. Within 15 minutes, the eReader automatically reports a negative eCup urine drug screen back to you via your account or another applicant tracking system. · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00867802000207), received between Jul 16, 2021 and Jul 16, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Melted” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Melted1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 16, 2021Melted; Melted

    ON (B)(6) 2021, COMPLAINT (B)(4) WAS RECEIVED. THE CUSTOMER REPORTED THAT "THE POWER CORD/ BOX FOR THEIR ESCREEN EREADER¿ HAS MELTED". NO ADVERSE PATIENT CONSEQUENCES WERE REPORTED. THIS EVENT HAS CONSERVATIVELY BEEN ASSESSED AS AN MDR REPORTABLE MALFUNCTION PENDING ADDITIONAL INVESTIGATION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12181690 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.