PowerPICCRecalls & reported problems across all models
Bard Access Systems, Inc. · 118 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
PowerPICC models — page 2
118 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- PowerPICC CK000553Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000561Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000444BCatheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000209ACatheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000631Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000671Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000676Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000417BCatheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000649Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000746Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000758Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000795Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC CK000871ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC CK000926Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC CK000592ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC CK000588BCatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC CK001011Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC 1174108D7Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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