PowerGlide Midline Catheter M122081Recalls & reported problems
Bard Access Systems, Inc. · PowerGlide Midline Catheter 22G, 8cm with Full Insertion Tray · Class 2
All models of PowerGlide Midline Catheter (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741038150), received between Jan 11, 2018 and Feb 26, 2019 — classified as 1 injury, 2 malfunctions.
The most frequently reported specific device problem is “Detachment Of Device Component” (2 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
- Detachment Of Device Component2
- Break1
- Difficult to Remove1
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.
InjuryFeb 26, 2019Break; Difficult to Remove
IT WAS REPORTED THAT THE LINE WAS PLACED SMOOTHLY WITHOUT ANY RESISTANCE BUT THE GUIDEWIRE WOULD NOT COME OUT. (B)(6) 2019 - ADDITIONAL INFORMATION RECEIVED: THE PLACER TOLD THE BD TM THAT THE GUIDEWIRE AND CATHETER INSERTED INTO THE PATIENT SMOOTHLY. WHEN SHE WENT TO REMOVE THE GUIDEWIRE, SHE FELT MORE RESISTANCE THAN NORMAL AND COULDN'T REMOVE THE WIRE. SHE TRIED PULLING AGAIN BUT WAS UNABLE TO REMOVE THE WIRE. A DOCTOR WAS CALLED WHO ALSO ATTEMPTED TO REMOVE THE WIRE WITHOUT SUCCESS. AT SOME POINT DURING MANIPULATION OF THE DEVICE, THE CATHETER BROKE FROM THE HUB. THE CATHETER AND WIRE WERE SUCCESSFULLY REMOVED FROM THE PATIENT. THE PLACER DID STATE THAT THE NEEDLE NEVER FULLY RETRACTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8370942 ↗MalfunctionFeb 16, 2018Detachment Of Device Component
IT WAS REPORTED BY THE FACILITY THAT THE ADHESIVE ON THE EXTENSION TUBING CAME APART. NO OTHER INFORMATION WAS PROVIDED. NO HARM TO THE PATIENT REPORTED. THIS FILE IS FOR SECOND DEVICE RETURNED FOR EVALUATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7278608 ↗MalfunctionJan 11, 2018Detachment Of Device Component
IT WAS REPORTED BY THE FACILITY THAT THE ADHESIVE ON THE EXTENSION TUBING CAME APART. NO OTHER INFORMATION WAS PROVIDED. NO HARM TO THE PATIENT REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7182124 ↗
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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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