PowerPICC SOLO CK000502ARecalls & 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741140822), received between Sep 11, 2020 and Sep 11, 2020 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Numbness1
- Tingling1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 11, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED VIA MS&S: "PATIENT'S DAUGHTER STATES THE PATIENT RECEIVED POWERPICC SOLO ON 08/05/2020. SHE REPORTS THAT THE CATHETER FLUSHES WITHOUT DIFFICULTY AND A BLOOD RETURN IS NOTED. THE PICC IS PLACED IN HER UPPER ARM. THE PATIENT REPORTS EXPERIENCING 'SHOCKS WITH NUMBNESS AND TINGLING' FROM HER ELBOW TO HER HAND ON THE SIDE OF THE PICC" MS&S RESPONSE: "DISCUSSED CAUSES OF THESE SYMPTOMS AND RECOMMENDED SHE CONTACT THE MD OR THE PICC TEAM AT THE HOSPITAL WHERE THE PICC WAS PLACED AND NOTIFY THEM AS SOON AS POSSIBLE. CASE FORWARDED TO FA VIA EMAIL" ADDITIONAL INFO. RECEIVED 08/24/2020 NO HARM REPORTED. WEIGHT: "(B)(6)" TREATED FOR:" LOW HEMOGLOBIN" OTHER RELATIVE HISTORY: "DIFFICULTY WITH GIVING OR RECEIVING BLOOD" "PATIENT DOES NOT HAVE AN INFECTIOUS DISEASE."
Patient problems: Numbness; Tingling
MAUDE report 10522613 ↗
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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