PowerGlide Midline Catheter M118101DRecalls & reported problems
Bard Access Systems, Inc. · PowerGlide Midline Catheter 18G, 10cm Max Barrier · Class 2
All models of PowerGlide Midline Catheter (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741038136), received between Dec 6, 2017 and Dec 6, 2017 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Break3
Patient problems
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2017Break
IT WAS REPORTED BY THE FACILITY THAT THE CLAMP BROKE ON THE END OF THE SLIDE. IT WAS STATED THE FACILITY USED CHG TO CLEAN THE CATHETER BUT NOT THE CLAMP. FACILITY CONTACT REPORTED THAT THE DRESSING IS CHANGED EVERY SIX DAYS WITH USE OF CHG AND THE CATHETER IS ACCESSED FOR INFUSION AND ASPIRATION EVERY EIGHT HOURS OR WITH INTERMITTENT USE. THE CLAMP BROKE AFTER A FEW DAYS OF USE. THIS REPORT ADDRESS THE SECOND CLAMP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7089378 ↗MalfunctionDec 6, 2017Break
IT WAS REPORTED BY THE FACILITY THAT THE CLAMP BROKE ON THE END OF THE SLIDE. IT WAS STATED THE FACILITY USED CHG TO CLEAN THE CATHETER BUT NOT THE CLAMP. FACILITY CONTACT REPORTED THAT THE DRESSING IS CHANGED EVERY SIX DAYS WITH USE OF CHG AND THE CATHETER IS ACCESSED FOR INFUSION AND ASPIRATION EVERY EIGHT HOURS OR WITH INTERMITTENT USE. THE CLAMP BROKE AFTER A FEW DAYS OF USE. THIS REPORT ADDRESS THE THIRD CLAMP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7089333 ↗MalfunctionDec 6, 2017Break
IT WAS REPORTED BY THE FACILITY THAT THE CLAMP BROKE ON THE END OF THE SLIDE. IT WAS STATED THE FACILITY USED CHG TO CLEAN THE CATHETER BUT NOT THE CLAMP. FACILITY CONTACT REPORTED THAT THE DRESSING IS CHANGED EVERY SIX DAYS WITH USE OF CHG AND THE CATHETER IS ACCESSED FOR INFUSION AND ASPIRATION EVERY EIGHT HOURS OR WITH INTERMITTENT USE. THE CLAMP BROKE AFTER A FEW DAYS OF USE. THIS REPORT ADDRESS THE FIRST CLAMP.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7089284 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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