CARDINAL HEALTH CAH4414Recalls & reported problems
Cardinal Health 200, LLC · Charging Station · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00885380048015), received between Feb 26, 2019 and Jun 27, 2019 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Overheating of Device” (5 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Overheating of Device5
Patient problems
- No Known Impact Or Consequence To Patient3
- No Patient Involvement2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 27, 2019Overheating of Device; Overheating of Device
BASED ON THE INFORMATION GATHERED FROM THE CUSTOMER THE SURGICAL CLIPPER CHARGING BASE NEARLY CAUGHT ON FIRE IN THE OPERATING ROOM. THE UNIT REPORTEDLY HAS A SMOKE STAIN ON IT AND THE OR SMELLED LIKE SMOKE FOR SEVERAL HOURS.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8739378 ↗MalfunctionApr 4, 2019Overheating of Device; Overheating of Device
THE SURGICAL CLIPPER CHARGER BASE WAS OVERHEATING, WAS WARM TO THE TOUCH. NO INJURY.
Patient problems: No Patient Involvement
MAUDE report 8482722 ↗MalfunctionApr 3, 2019Overheating of Device; Overheating of Device
A BURNT ODOR WAS COMING FROM SURGICAL CLIPPER CHARGING BASE SO THE CUSTOMER STOPPED USING IT. THERE WAS NO INJURY.
Patient problems: No Patient Involvement
MAUDE report 8480358 ↗MalfunctionFeb 28, 2019Overheating of Device; Overheating of Device
THE CUSTOMER NOTICED THE SURGICAL CLIPPER CHARGING BASE WAS VERY HOT. THEY DID NOT WANT TO TAKE ANY CHANCES AND REMOVED IT FROM THE DEPARTMENT. NO INJURY BUT CUSTOMER WAS WORRIED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8377580 ↗MalfunctionFeb 26, 2019Overheating of Device; Overheating of Device
A NURSE NOTICED A BURNING SMELL AND REALIZED THAT IT WAS COMING FROM THE SURGICAL CLIPPER CHARGING BASE. NO INJURY BUT CUSTOMER IS VERY CONCERNED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8371795 ↗
Other RAZOR, SURGICAL devices
- 3M™ 96603m Company · RAZOR, SURGICAL1 recall0 reports
- 3M™ 96903m Company · RAZOR, SURGICAL1 recall0 reports
- N/A 4406Carefusion 2200, Inc · RAZOR, SURGICAL17 reports
- MEDLINE CLIP5515Medline Industries, Inc. · RAZOR, SURGICAL6 reports
- 3M™ 96903m Company · RAZOR, SURGICAL2 reports
- SensiClip 4403ACarefusion 2200, Inc · RAZOR, SURGICAL1 report
- Medline DYND70880Medline Industries, Inc. · RAZOR, SURGICAL1 report
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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