PowerGlide Pro F422088PTRecalls & reported problems
Bard Access Systems, Inc. · Catheter Placement Kit · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741232121), received between Mar 10, 2026 and Aug 4, 2026 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Product Quality Problem1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 4, 2026Break
It was reported that a Vascular Access Nurse placed a 20g 10cm PowerGlide catheter. Needle was inserted, wire advanced and engaged & catheter advanced. The catheter became severed from the blue portion of the hub during the process of retracting the wire and was lodged inside the patient¿s vessel. Vascular Survey was called in to perform a cutdown with catheter retrieval. Retained catheter in vascular, removed by vascular surgeon. No further details provided.
Patient problems: Foreign Body In Patient
MAUDE report 50130383 ↗MalfunctionMar 10, 2026Product Quality Problem
IT WAS REPORTED THAT PROBE COVER ON POWERGLIDE HAD HOLES. NO PATIENT IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24563156 ↗
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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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