PowerPICC SOLO CK000504Recalls & reported problems
Bard Access Systems, Inc. · Catheter Placement Kit · Class 2 · Implant
All models of PowerPICC SOLO (78)
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 00801741100116), received between Aug 18, 2017 and Aug 18, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Flushing Problem” (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
- Flushing Problem1
- Occlusion Within Device1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2017Flushing Problem; Occlusion Within Device
PATIENT REPORTED TO MEDICAL SERVICES THAT HE HAD A POWER PICC SOLO SINGLE LUMEN PLACED ON (B)(6) 2017, FOR DAILY IV MEDICATION. THE PICC WORKED WELL YESTERDAY. WHEN DRESSING WAS CHANGED, THE PATIENT STATED THE CATHETER WANTED TO KINK. WHEN PATIENT ATTEMPTED TO GET MEDICATION TODAY THE PICC WOULD NOT FLUSH. ADVISED THE PATIENT TO CONTACT THE NURSE ABOUT CHANGING THE PICC DRESSING OR ACCESS LINE FOR OCCLUSION DUE TO POSSIBLE FIBRIN. ON (B)(6) 2017 - ADDITIONAL INFORMATION REPORTED THAT THE PATIENT WENT TO THE EMERGENCY ROOM WHERE THEY CHANGED THE LEUR HUB ON THE CATHETER. CATHETER FLUSHES AND ASPIRATES WITHOUT DIFFICULTY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 6803429 ↗
Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices
- Groshong NXT ClearVue Catheter 7617405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,708 reports
- Groshong NXT ClearVue Catheter 7655405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,536 reports
- PowerPICC Catheter 3174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall402 reports
- L-Cath™ S/L PICC S/L 26GA (1.9F) x 30cmArgon Medical Devices, Inc. · Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days2 recalls245 reports
- PowerPICC SOLO2 Catheter 1194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls216 reports
- Broviac 0600520Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall265 reports
- Groshong® Catheter 7717405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days279 reports
- PowerPICC Catheter 3275118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days272 reports
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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