Silicone Evacuator Kit 0073310Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741050053), received between Aug 18, 2025 and Nov 13, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Disconnection” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionNov 13, 2025Disconnection; Disconnection

  IT WAS REPORTED THAT THE CUSTOMER ASKED FOR ANY ALTERNATIVES TO THE 0043610 HEMOVAC DRAIN KIT BECAUSE THEY WERE HAD ISSUES WITH THE DRAIN KEPT DISCONNECTING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23542960 ↗
• MalfunctionAug 18, 2025Disconnection; Disconnection

  IT WAS REPORTED THAT THE PATIENT HAS A BULB (JP) DRAIN THAT CAME DISCONNECTED FROM THE TUBING. DRAIN WAS CLEANED AND PLACED BACK TOGETHER BY FLOOR NURSES. THE TUBE WAS PLACED INSIDE THE BULB CONNECTION AS IT COULD NOT FIT OVER THE CONNECTION. THE TUBE WAS TAPED AT THE CONNECTION TO THE BULB. THIS WAS A DAVOL DRAIN. COULD NOT DETERMINE THE EXACT PRODUCT CODE. SAMPLE SAVED FOR VENDOR CONFIRMATION. THE DRAIN WAS PLACED DURING A SPINAL SURGERY. THERE WAS NO SERIOUS HARM REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22827873 ↗