MEDLINE CLIP5515Recalls & reported problems
Medline Industries, Inc. · CLIPPER, SURGICAL, LED, CHARGER & BASE · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10193489016963), received between Apr 24, 2026 and Jun 17, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Failure to Charge” (3 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Charge3
- Break2
- Material Fragmentation1
Patient problems
- Insufficient Information5
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 17, 2026Break
IT WAS REPORTED THAT THEY HAD A BROKEN CLIPPER HANDLE. THE PLASTIC PIECE THAT HOLDS ON THE BLADE WAS BROKEN ON ONE SIDE, AND THE BLADE CAN NO LONGER BE ATTACHED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25540695 ↗MalfunctionJun 16, 2026Failure to Charge
IT WAS REPORTED THAT THE PRODUCT SHOWS AS CHARGING, BUT WHEN REMOVED FROM THE CHARGING STATION TO USE, THEY DO NOT TURN ON.
Patient problems: Insufficient Information
MAUDE report 25526870 ↗MalfunctionJun 10, 2026Failure to Charge
IT WAS REPORTED THAT A SURGICAL CLIPPER HANDLE STOPPED WORKING AND WILL NOT HOLD A CHARGE AND EVENTUALLY DIES.
Patient problems: Insufficient Information
MAUDE report 25465905 ↗MalfunctionJun 9, 2026Failure to Charge
IT WAS REPORTED THAT THE DEVICE WAS NOT CHARGING.
Patient problems: Insufficient Information
MAUDE report 25449267 ↗MalfunctionMay 29, 2026Break
IT WAS REPORTED THAT THE BLADE HOLDER WAS DAMAGED.
Patient problems: Insufficient Information
MAUDE report 25340667 ↗MalfunctionApr 24, 2026Material Fragmentation
CUSTOMER REPORTED, "WE HAD A BROKEN CLIPPER REPORTED TODAY. IT BROKE AT THE LITTLE WHITE PIECE THAT HOLDS THE BLADE."
Patient problems: Insufficient Information
MAUDE report 24987897 ↗
Other RAZOR, SURGICAL devices
- 3M™ 96903m Company · RAZOR, SURGICAL1 recall0 reports
- 3M™ 96603m Company · RAZOR, SURGICAL1 recall0 reports
- N/A 4406Carefusion 2200, Inc · RAZOR, SURGICAL17 reports
- CARDINAL HEALTH CAH4414Cardinal Health 200, LLC · RAZOR, SURGICAL5 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page