ADVIA Autoslide® Slide Maker Stainer 10318817Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00630414517360), received between Sep 8, 2017 and Sep 8, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Handling Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionSep 8, 2017Mechanical Problem; Device Handling Problem; Mechanical Problem; Device Handling Problem

  A CUSTOMER'S FACE WAS SPLASHED WITH AUTOSLIDE RINSE SOLUTION AND POTENTIALLY BIOHAZARDOUS MATERIAL WHILE PERFORMING A TROUBLESHOOTING PROCESS ON THE ADVIA AUTOSLIDE SYSTEM. THE CUSTOMER INDICATED THAT THE RINSE WELL WAS BLOCKED AND POTENTIALLY CONTAINED WHOLE BLOOD DILUTION. THE CUSTOMER WAS WEARING A LAB COAT AS PERSONAL PROTECTIVE EQUIPMENT AT THE TIME OF THE INCIDENT. THE CUSTOMER USED EYEWASH FLUID AND WATER TO RINSE HER EYE OF THE LIQUID THAT SPLASHED INTO HER EYE. MEDICAL INTERVENTION BEYOND FIRST AID WAS NOT REQUIRED. THERE ARE NO KNOWN REPORTS OF ADVERSE HEALTH CONSEQUENCES DUE TO THE LIQUID THAT SPLASHED INTO THE CUSTOMER'S EYE AND THERE WERE NO REPORTS OF IMPACT TO PATIENT RESULTS.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6852392 ↗