PowerPICC CatheterRecalls & reported problems across all models
Bard Access Systems, Inc. · 33 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name at least one PowerPICC Catheter model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1,014
- Deaths reported
- 1
- Injuries reported
- 86
- Recalls
- 3
We found 33 models of PowerPICC Catheter by Bard Access Systems, Inc. in the FDA's device registry (GUDID). Together they are named in 1,014 adverse event reports in the FDA's MAUDE database, received between Dec 4, 2015 and Sep 24, 2026 — classified as 1 death, 86 injuries, 927 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (479 reports).
3 FDA recall records name at least one of these models by its device identifier, 2 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
PowerPICC Catheter recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 21, 2026Open, Classified
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Z-2666-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
- Mar 11, 2025Open, Classified
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.
Z-1507-2025 · Root cause: Process control · names 7 of these models · Recall details · FDA record ↗
- May 19, 2021Terminated
Catheter kits contained the incorrect micro-introducers.
Z-1991-2021 · Root cause: Process control · Recall details · FDA record ↗
Most reported PowerPICC Catheter problems
Device problems
- Fluid/Blood Leak479
- Material Deformation140
- Defective Component85
- Material Frayed69
- Contamination /Decontamination Problem65
- Break59
- Adverse Event Without Identified Device or Use Problem21
- Leak/Splash18
Patient problems
- No Clinical Signs, Symptoms or Conditions708
- No Known Impact Or Consequence To Patient98
- No Consequences Or Impact To Patient64
- Foreign Body In Patient37
- Pain30
- Swelling/ Edema22
- Thrombosis/Thrombus17
- Extravasation15
PowerPICC Catheter models
33 models, most reported first. Each model has its own page with its reports, recalls and device details.
- PowerPICC Catheter 3174118Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall402 reports
- PowerPICC Catheter 3275118Catheter,intravascular,therapeutic,long-term greater than 30 days272 reports
- PowerPICC Catheter 3174155Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall26 reports
- PowerPICC® Catheter 3174335Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall15 reports
- PowerPICC Catheter 3174355Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall12 reports
- PowerPICC® Catheter 3174108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall9 reports
- PowerPICC® Catheter 3174108Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC® Catheter 3275108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 recall5 reports
- PowerPICC Catheter 3175155Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall4 reports
- PowerPICC Catheter 3174135Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall3 reports
- PowerPICC Catheter 3275355Catheter,intravascular,therapeutic,long-term greater than 30 days43 reports
- PowerPICC Catheter 3275335Catheter,intravascular,therapeutic,long-term greater than 30 days1 death36 reports
- PowerPICC Catheter 3275155Catheter,intravascular,therapeutic,long-term greater than 30 days25 reports
- PowerPICC Catheter 3275135Catheter,intravascular,therapeutic,long-term greater than 30 days22 reports
- PowerPICC® Catheter 9275108DCatheter,intravascular,therapeutic,long-term greater than 30 days22 reports
- PowerPICC Catheter 3276135Catheter,intravascular,therapeutic,long-term greater than 30 days21 reports
- PowerPICC® Catheter 3275108Catheter,intravascular,therapeutic,long-term greater than 30 days18 reports
- PowerPICC Catheter 3175335Catheter,intravascular,therapeutic,long-term greater than 30 days18 reports
- PowerPICC Catheter 3175118Catheter,intravascular,therapeutic,long-term greater than 30 days12 reports
- PowerPICC Catheter 3175135Catheter,intravascular,therapeutic,long-term greater than 30 days9 reports
- PowerPICC Catheter 3175355Catheter,intravascular,therapeutic,long-term greater than 30 days7 reports
- PowerPICC Catheter 3276118Catheter,intravascular,therapeutic,long-term greater than 30 days6 reports
- PowerPICC Catheter 3386105Catheter,intravascular,therapeutic,long-term greater than 30 days6 reports
- PowerPICC® Catheter 3276155Catheter,intravascular,therapeutic,long-term greater than 30 days4 reports
- PowerPICC® Catheter 3386108Catheter,intravascular,therapeutic,long-term greater than 30 days2 reports
- PowerPICC Catheter 3386335Catheter,intravascular,therapeutic,long-term greater than 30 days2 reports
- PowerPICC® Catheter 9275108Catheter,intravascular,therapeutic,long-term greater than 30 days2 reports
- PowerPICC® Catheter 3175108Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC® Catheter 3175108DCatheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Catheter 3276355Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Catheter 3386155Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC Catheter 3386355Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
- PowerPICC® Catheter 9275118Catheter,intravascular,therapeutic,long-term greater than 30 days1 report
Recent PowerPICC Catheter adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50887523 ↗MalfunctionSep 23, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50874624 ↗MalfunctionSep 23, 2026Material Deformation
It was reported on April 1, 2026, during a PICC replacement procedure, the package of the peripherally inserted central catheter (PICC) was opened and inspected. It was found that the peelable split sheath had a raised/protruding tip. The device was immediately replaced with a new one. No apparent harm occurred.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50868115 ↗MalfunctionSep 10, 2026Material Deformation
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50716232 ↗MalfunctionSep 10, 2026Fluid/Blood Leak
It was reported a fluid leak was discovered 1 cm below the red port of the Extension Tubing during intravenous infusion with the PowerPICC catheter. Following the leakage, the catheter was promptly replaced to continue treatment. However, as the patient was on the second day after a stem cell transplant and had compromised immunity, reinsertion of the catheter posed risks such as catheter-related injury, bleeding, and infection. The patient is currently hospitalized for observation. No further information was provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714878 ↗MalfunctionSep 10, 2026Fluid/Blood Leak
It was reported a fluid leak was discovered 1 cm below the red port of the Extension Tubing during intravenous infusion with the PowerPICC catheter. Following the leakage, the catheter was promptly replaced to continue treatment. However, as the patient was on the second day after a stem cell transplant and had compromised immunity, reinsertion of the catheter posed risks such as catheter-related injury, bleeding, and infection. The patient is currently hospitalized for observation. No further information was provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714876 ↗MalfunctionSep 10, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50714874 ↗MalfunctionSep 9, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50700874 ↗MalfunctionAug 31, 2026Fluid/Blood Leak
It was reported after two months of use, the patient discovered fluid leakage and broken tubing. No further information was provided.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533109 ↗MalfunctionAug 31, 2026Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533107 ↗MalfunctionAug 31, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533105 ↗MalfunctionAug 26, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50454711 ↗MalfunctionAug 26, 2026Contamination /Decontamination Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50452722 ↗MalfunctionAug 19, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50328787 ↗MalfunctionAug 12, 2026Fluid/Blood Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50220513 ↗
Other Bard Access Systems, Inc. products
- Port Access Needle122 models · 3,744 reports · 3 recalls
- Groshong NXT ClearVue Catheter8 models · 3,266 reports
- PowerPort ClearVUE27 models · 1,993 reports · 15 recalls
- Site~Rite 8 Ultrasound System11 models · 1,965 reports
- PowerPort M.R.I., ChronoFlex22 models · 1,642 reports · 1 recall
- PowerPICC Provena116 models · 1,337 reports · 2 recalls
- PowerPort M.R.I., Groshong10 models · 1,285 reports
- Navarre15 models · 1,228 reports
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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