Monoject 8985PG2YRecalls & reported problems
Cardinal Health, Inc. · Monoject™ Sharps Container, PGII, Hinged Lid, Yellow, 8 Gallon · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521154244), received between Oct 29, 2021 and Oct 29, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component or Accessory Incompatibility” (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
Device problems
- Component or Accessory Incompatibility1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 29, 2021Component or Accessory Incompatibility; Component or Accessory Incompatibility
THE CUSTOMER REPORTED THAT SHARP CONTAINERS ARE EXTREMELY DIFFICULT TO SEAL. THERE HAVE BEEN NUMEROUS INCIDENTS WHERE NURSING STAFF WAS UNABLE TO CLICK ALL THE LATCHES DUE TO THEIR PHYSICAL ABILITY TO PROVIDE ENOUGH STRENGTH TO DO SO. THE LIDS JUST WON'T CLOSE. THE NURSES ARE EXPERIENCING PHYSICAL PAIN IN ARMS AND HANDS
Patient problems: Pain
MAUDE report 12721343 ↗
Other Container, sharps devices
- SharpSafety 8556HCardinal Health, Inc. · Container, Sharps65 reports
- Monoject 8507SACardinal Health, Inc. · Container, sharps13 reports
- BD Recykleen™ Sharps Collector 305160Becton, Dickinson And Company · Container, sharps6 reports
- Monoject 31142222Cardinal Health, Inc. · Container, sharps4 reports
- Monoject 8506YCardinal Health, Inc. · Container, sharps4 reports
- Monoject 8980SCardinal Health, Inc. · Container, sharps4 reports
- Monoject 8970YCardinal Health 200, LLC · Container, Sharps3 reports
- Monoject 85221RCardinal Health, Inc. · Container, sharps3 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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