Monoject 8936PG2Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 40884521022431), received between Apr 28, 2021 and May 17, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Difficult to Open or Close” (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

Recent adverse event reports

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

• MalfunctionMay 17, 2021Separation Problem; Separation Problem

  THE CUSTOMER REPORTED THAT THE LID APPEARS TO SNAP DOWN BUT THEN CAN LIFT STRAIGHT UP AND DOES NOT CONTAIN THE CONTENTS WHICH IS A SAFETY HAZARD. NO PATIENT INJURY WAS REPORTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11837769 ↗
• MalfunctionApr 28, 2021Difficult to Open or Close; Difficult to Open or Close

  THE CUSTOMER REPORTED THE CONTAINER LID IS DIFFICULT TO CLOSE. AFTER SEVERAL ATTEMPTS TO CLOSE, THE LID CONTINUES TO LIFT. IT TOOK ABOUT 5 MINUTES WITH EACH CONTAINER WITH CONTINUED ATTEMPTS AT CLOSING THE LID TO SUCCEED. CONTAINERS WERE CLOSED PROPERLY AFTER MANY ATTEMPTS AND SENT FOR PROPER DISPOSAL.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11740649 ↗