PowerPICC Provena CK000766Recalls & reported problems
Bard Access Systems, Inc. · Catheter Placement Kit · Class 2 · Implant
All models of PowerPICC Provena (116)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741141751), received between Feb 24, 2018 and Jul 23, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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
- Break2
Patient problems
- No Information1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 23, 2019Break
IT WAS REPORTED THAT "THE INSERTER WENT TO BEND THE WIRE OUTSIDE OF THE STYLET AND IT BROKE OFF."
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8818224 ↗MalfunctionFeb 24, 2018Break
IT WAS REPORTED BY THE FACILITY THAT THE PICC WAS PLACED IN THE PATIENT'S RIGHT UPPER EXTREMITY AND ON (B)(6) 2017 WAS NOTED TO BE BROKEN BETWEEN THE CATHETER AND THE HUB.
Patient problems: No Information
MAUDE report 7294465 ↗
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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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