Sharps-A-Gator 8881676236Recalls & reported problems
Cardinal Health, Inc. · Sharps Container,Chimney Top, Red · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521018853), received between Nov 24, 2020 and Dec 1, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break1
- Difficult to Open or Close1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 1, 2020Break; Break
THE CUSTOMER REPORTS THE TABS ON THE LID ARE BREAKING. THERE WAS NO PATIENT HARM.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10927719 ↗MalfunctionNov 24, 2020Difficult to Open or Close; Difficult to Open or Close
THE CUSTOMER REPORTED THAT THE TABS ARE BREAKING. ADDITIONAL INFORMATION RECEIVED FROM THE INITIAL REPORTER STATED THAT TABS ARE BREAKING MEANS THE LID WOULD NOT BE ABLE TO LOCK IN PLACE. THERE WAS NO REPORTED INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10891966 ↗
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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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