PowerGlide Midline Catheter M020101Recalls & reported problems
Bard Access Systems, Inc. · PowerGlide, 20g10cm Full · Class 2
All models of PowerGlide Midline Catheter (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00801741075308), received between Sep 29, 2022 and Mar 26, 2026 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Defective Component” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Defective Component3
- Improper or Incorrect Procedure or Method3
- Activation Problem1
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Foreign Body In Patient1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 26, 2026Activation Problem
IT WAS REPORTED THAT ISSUE WITH POWERGLIDE. NEEDLE GOT STUCK AND UNABLE TO RETRACT FULLY MAKING THE CATHETER UNABLE TO BE USED. PATIENT HAD TO BE STUCK AGAIN. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24702402 ↗MalfunctionJul 9, 2024Defective Component; Defective Component
IT WAS REPORTED THAT THE MIDLINE CATHETER SEPARATED WHILE THE NURSE WAS PLACING THE MIDLINE. ADDITIONAL INFORMATION JUNE 24: IT WAS REPORTED THE NEGATIVE OUTCOME WAS THAT THE PATIENT HAD TO HAVE THE LINE PULLED AND REPLACED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19704982 ↗MalfunctionJan 6, 2023Improper or Incorrect Procedure or Method; Defective Component; Improper or Incorrect Procedure or Method; Defective Component
IT WAS REPORTED BY THE CUSTOMER THAT "TWO LINES SPLIT ABOUT AN INCH FROM THE TIP DURING INSERTION." NO OTHER INFORMATION WAS PROVIDED. THIS REPORT ADDRESSES THE FIRST DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16112118 ↗MalfunctionJan 6, 2023Improper or Incorrect Procedure or Method; Defective Component; Improper or Incorrect Procedure or Method; Defective Component
IT WAS REPORTED BY THE CUSTOMER THAT "TWO LINES SPLIT ABOUT AN INCH FROM THE TIP DURING INSERTION." NO OTHER INFORMATION WAS PROVIDED, THIS REPORT ADDRESSES THE SECOND DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16112013 ↗InjurySep 29, 2022Break; Improper or Incorrect Procedure or Method; Break; Improper or Incorrect Procedure or Method
IT WAS REPORTED BY THE CUSTOMER "SHEERED OFF PART OF A POWERGLIDE IN THE PATIENT ABOUT 2CM. THIS WAS DUE TO CLINICIAN INSERTION ERROR."
Patient problems: Foreign Body In Patient
MAUDE report 15505468 ↗
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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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