Sharps-A-Gator 31156550Recalls & reported problems
Cardinal Health, Inc. · True content to be populated as part of rebranding · Class 2
Data updated Oct 18, 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 30884521042838), received between Mar 24, 2020 and Mar 24, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Incompatible” (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
Device problems
- Component Incompatible1
- Material Deformation1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 24, 2020Component Incompatible; Material Deformation; Component Incompatible; Material Deformation
THE CUSTOMER REPORTED THAT THE CONTAINERS DO NOT SIT FLUSH ON A SURFACE. ADDITIONAL INFORMATION WAS RECEIVED FROM THE CUSTOMER THAT WHEN SEALING THE SHARPS FOR PROPER DISPOSAL, THE LATCHES THAT KEEP THE LID LOCKED ARE NOT SECURE AND RE-OPEN. ALSO, THE SHARPS DO NOT HAVE A FLAT BOTTOM WHERE THE SHARPS CAN SIT FLUSH TO THE TABLE, DESK OR COMPUTER CART. WHEN THAT HAPPENS IT TENDS TO GET MOVED AROUND LEADING TO TIPPING OVER. IF THE SHARPS ARE FULL ENOUGH, IT HAS CAUSED A SPILLAGE OF USED SHARPS.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9873907 ↗
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 8980SCardinal Health, Inc. · Container, sharps4 reports
- Monoject 8506YCardinal Health, Inc. · Container, sharps4 reports
- Monoject 31142222Cardinal Health, Inc. · Container, sharps4 reports
- Monoject 85221RCardinal Health, Inc. · Container, sharps3 reports
- Monoject 8970YCardinal Health 200, LLC · 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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