PowerPICC ProvenaRecalls & reported problems across all models
Bard Access Systems, Inc. · 116 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
PowerPICC Provena models — page 2
116 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- PowerPICC Provena CK000803Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Provena CK000823Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Provena CK000846Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Provena S1193108D1Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000186BCatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000759ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000909ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000954Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000410ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000853Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000951Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000952Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000904ACatheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena CK000985Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena S1274108D7Catheter, intravascular, therapeutic, long-term greater than 30 days1 report
- PowerPICC Provena S1385108D7Catheter, 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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