Accelerator II, Aspirator (110V) ASP IIRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00081317020028), received between Feb 9, 2018 and Dec 6, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Backflow” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 6, 2022Failure to Power Up; Failure to Power Up

  IT WAS REPORTED THAT AN ACCELERATOR II, ASPIRATOR (110V) EXPERIENCED AN ELECTRICAL FAULT. NO ADVERSE EVENT WAS EXPERIENCED BY A PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15926316 ↗
• MalfunctionMay 23, 2018Improper Flow or Infusion; Improper Flow or Infusion

  IT WAS REPORTED THAT A NURSE SET UP A MENTOR ACCELERATOR II, ASPIRATOR (110V) DEVICE INCORRECTLY AND BIOBURDEN WAS TRANSFERRED INSIDE THE UNIT DURING AN UNSPECIFIED PROCEDURE. FLUID WAS FOUND INSIDE THE MOTOR. THIS INCIDENT DID NOT CAUSE INJURY TO A PATIENT OR USER.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7538963 ↗
• MalfunctionFeb 9, 2018Backflow; Backflow

  IT WAS REPORTED THAT DURING A FAT GRAFTING PROCEDURE PERFORMED WITH AN ACCELERATOR II ASPIRATOR, FLUID WAS SUCKED INTO THE GENERATOR. PER CUSTOMER, THERE WAS NO INJURY TO THE PATIENT OR THE USER OF THE DEVICE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7261568 ↗