SharpSafety 8537SARecalls & reported problems
Cardinal Health, Inc. · Safety In Room Sharps Container,Counterbalance Lid, Transparent Red · Class 2
All models of SharpSafety (7)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20884521077253), received between Jan 9, 2024 and Jan 9, 2024 — classified as 1 injury.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 9, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE CUSTOMER REPORTED THAT A NEEDLE WAS POKING OUT OF THE SHARPS CONTAINER AND CUSTOMER WAS POKED. CUSTOMER WENT TO THE HOSPITAL. ADDITIONAL INFORMATION RECEIVED ON (B)(6) 2023 STATED THAT THE EMPLOYEE WAS GIVEN MEDICATIONS FOR THE TREATMENT TO PREVENT HIV SINCE THE NEEDLE IS FROM AN UNKNOWN SOURCE. THE EMPLOYEE ALSO HAD AN HIV TEST AND A HEPATITIS PANEL DRAWN. THE RESULTS ARE NEGATIVE. THE EMPLOYEE WILL HAVE FOLLOW UP LABS FOR ONE YEAR. ON (B)(6) 2024 THE CUSTOMER CONFIRMED THE NEEDLE WAS STICKING THROUGH THE WALL OF THE CONTAINER.
Patient problems: Needle Stick/Puncture
MAUDE report 18480974 ↗
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 8970YCardinal Health 200, LLC · Container, Sharps3 reports
- Monoject 8932PG2Cardinal 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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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