Ear and Ulcer Syringe 9005290Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801741076029), received between Jan 19, 2021 and Jan 19, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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.

• MalfunctionJan 19, 2021Device Contamination with Chemical or Other Material; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT THERE WAS WHITE POWDER IN COMPONENTS OF EAR SYRINGE PER CUSTOMER RESPONDED BACK TO THE FOLLOW UP ON (B)(6) 021, STATED THAT THE WHITE POWDER WAS ON JUST OUTSIDE THE DEVICE AND ALL OF THE 6,327 HAS 100 DEFECT FROM THE INSPECTION.

  Patient problems: No Patient Involvement

  MAUDE report 11198513 ↗