Pro-PICC® CT MR82036301Recalls & reported problems
Medical Components, Inc. · 6F X 60CM TRIPLE LUMEN Pro-PICC® CT W/VALVE TECHNOLOGY BASIC IR SET · Class 2 · Implant
All models of Pro-PICC CT (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00884908101812), received between Jan 4, 2023 and Jan 17, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Break” (3 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 16, 2026.
Most reported problems
Device problems
- Break3
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 17, 2023Break; Break
BREAKAGE OF THE BI-DIRECTIONAL VALVE ON THE YELLOW TRACT WHICH SEPARATED INTO TWO PIECES DURING POST-SAMPLING IRRIGATION WITH 10 ML SYRINGE OF 0.9% NACL AFTER CHANGING NEEDLE-LESS CONNECTOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16185477 ↗MalfunctionJan 17, 2023Break; Break
BREAKAGE OF THE BI-DIRECTIONAL VALVE ON THE YELLOW TRACT WHICH SEPARATED INTO TWO PIECES DURING POST-SAMPLING IRRIGATION WITH 10 ML SYRINGE OF 0.9% NACL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16185330 ↗MalfunctionJan 4, 2023Break; Break
BREAKAGE OF THE BI-DIRECTIONAL VALVE ON THE YELLOW TRACT WHICH SEPARATED INTO TWO PIECES DURING POST-SAMPLING IRRIGATION WITH 10 ML SYRINGE OF 0.9% NACL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16093719 ↗
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® Catheters 1174108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall222 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page