Monoject 85121Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521022683), received between Nov 19, 2019 and Nov 19, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 19, 2019Break; Break

  THE CUSTOMER REPORTED THE LID OF THE SHARPS CONTAINER BREAKS. THE CUSTOMER FURTHER STATED WHEN PUSHING IN THE LEFT HAND SIDE OF THE ORANGE PORTION, IT COMPLETELY COLLAPSES AND DOESN'T ALLOW THEM TO PUSH DOWN ON IT AT ALL BECAUSE IT FALLS RIGHT INSIDE. THE EMPLOYEE'S FINGER WENT INTO THE CONTAINER BUT THERE WAS NO INJURY OR HARM.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9341589 ↗
• MalfunctionNov 19, 2019Break; Break

  THE CUSTOMER REPORTED THAT THE LID OF THE SHARPS CONTAINER BREAKS. WHEN SHUTTING THE LID, THEIR HAND ALMOST GOES INSIDE THE ITEM. WHEN PUSHING IN THE LEFT HAND SIDE OF THE ORANGE PORTION, IT COMPLETELY COLLAPSES AND IT DOESN'T ALLOW THEM TO PUSH DOWN ON IT AT ALL BECAUSE IT FALLS RIGHT INSIDE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 9341583 ↗