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405TSRVS-SIRecalls & reported problems

Agilent Technologies, Inc. · Microplate Washer · Class 1

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 05700574034061), received between Jul 13, 2023 and Jul 13, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Smoking” (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

  • Smoking1

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 13, 2023Smoking; Smoking

    CUSTOMER FROM GERMANY REPORTED A PROBLEM WITH BIOTEK 405 TS WASHER. THE DEVICE PRODUCED SMOKE WHEN OPERATED. THE CAUSE OF THIS ISSUE HAS NOT YET BEEN FOUND. THE SMOKE STOPPED AFTER SWITCHING OFF THE INSTRUMENT. CURRENTLY THE INSTRUMENT IS NOT WORKING. NO DIRECT OR INDIRECT PATIENT HARM OR USER HARM HAVE BEEN REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17316839 ↗

Other STATION, PIPETTING AND DILUTING, FOR CLINICAL USE devices

All STATION, PIPETTING AND DILUTING, FOR CLINICAL USE devices →

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