PowerGroshong Catheter 7918508Recalls & reported problems
Bard Access Systems, Inc. · DOT PowerGRO, 5Fr SL, · Class 2 · Implant
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 00801741028540), received between Aug 30, 2017 and Aug 30, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (1 report).
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
- Fracture1
Patient problems
- Foreign Body In Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 30, 2017Fracture
IT WAS REPORTED THAT THE PICC WAS PLACED IN THE PATIENT'S LEFT UPPER ARM ON (B)(6) 2017. IT WAS DISCONTINUED ON (B)(6) 2017 AND NOTED TO BE ONLY 10CM IN LENGTH. SUBSEQUENT CHEST X-RAY REVEALED THE FRACTURED PICC LOCATED IN THE LEFT AXILLARY VEIN RUNNING TO THE RIGHT ATRIUM. THE PATIENT WAS TRANSFERRED TO ANOTHER FACILITY WHERE SHE UNDERWENT SUCCESSFUL REMOVAL ON (B)(6) 2017 AND DISCHARGED ON (B)(6) 2017.
Patient problems: Foreign Body In Patient
MAUDE report 6832687 ↗
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- 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
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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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