PowerGlide F118081TRecalls & reported problems
Bard Access Systems, Inc. · PowerGlide Pro with Reinforced Tip, 18G 8cm, Full Kit · Class 2
All models of PowerGlide (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741142697), received between May 4, 2023 and May 4, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Component Incompatible” (1 report).
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
- Component Incompatible1
- Defective Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 4, 2023Component Incompatible; Defective Component; Component Incompatible; Defective Component
IT WAS REPORTED BY THE CUSTOMER" GUIDEWIRE RECOILED WHEN HE WAS CHECKING IT PRIOR TO INSERTION." ADDITIONAL INFORMATION RECEIVED 04/18/2023: IT WAS REPORTED BY THE CUSTOMER "WHEN I WAS CHECKING THE GUIDEWIRE BEFORE USING THE MIDLINE CATHETER, I NOTICED THAT I COULD ADVANCE THE SLIDE, BUT THE GUIDEWIRE WOULD NOT ADVANCE. UPON FURTHER EVALUATION, IT LOOKS LIKE THE GUIDEWIRE RECOILED INTO THE DEVICE. I HAD NOT YET POKED THE PATIENT, AS WE WERE TAUGHT TO MAKE SURE THE GUIDEWIRE IS INTACT EVEN BEFORE INSERTION. THE PRODUCT I WAS USING WAS THE MIDLINE CATHETER KIT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16869413 ↗
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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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