Devices › Port & catheter, implanted, subcutaneous, intravascular
Device brand name · Port & catheter implanted subcutaneous intravascular
Power Port isp M.R.I., 8Fr Groshong: medical device reports filed with FDA
225 reports name it, 2019–2026. Manufacturer given most often on reports: C R Bard Basd -3006260740. Product code LJT.
- 225
- device reports naming the brand
- 0% of all MAUDE reports · about 32 a year
- 36
- reports, 12 months to August 2026
- 38 in the 12 months before
- 75.6%
- classified as malfunction
- 38.6% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 225 reports that name the brand "Power Port isp M.R.I, 8Fr Groshong" (port & catheter implanted subcutaneous intravascular), received between July 2019 and May 2026; the manufacturer given most often on reports is C R Bard Basd -3006260740. Spellings of one product vary from report to report.
36 reports arrived in the 12 months to August 2026, close to the 38 of the 12 months before. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases. The event types recorded are malfunction (75.6%) and injury (24.4%); across all port & catheter, implanted, subcutaneous, intravascular reports (product code LJT) death is recorded in 1.8% and malfunction in 38.6%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are fracture (64.4%), deformation due to compressive stress (37.8%) and naturally worn (28%). The patient problems coded most often are appropriate clinical signs, symptoms and conditions term/code not available, extravasation and pain. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Reports by month, five years
Reports by the month FDA received them. FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 22,475 reports carrying product code LJT. Event type is the filer's classification and is not verified by FDA.
Device problems coded
| Device problem (FDA code) | Reports | Share | Share across product code |
|---|---|---|---|
| Fracturea broken bone | 145 | 64.4% | 23.6% |
| Deformation due to compressive stress | 85 | 37.8% | 5.7% |
| Naturally worn | 63 | 28% | 2.8% |
| Fluid/blood leak | 59 | 26.2% | 9.1% |
| Material separation | 57 | 25.3% | 9% |
| Migrationthe device moved from where it was placed | 23 | 10.2% | 5.6% |
| Suction problem | 21 | 9.3% | 4.5% |
| Obstruction of flow | 13 | 5.8% | 3.7% |
| Difficult to flush | 12 | 5.3% | 3.5% |
| Air/gas in device | 9 | 4% | 0.6% |
| Failure to advance | 8 | 3.6% | 1.1% |
| Difficult to insertthe device was hard to insert | 6 | 2.7% | 1.4% |
| Component missing | 5 | 2.2% | 1.2% |
| Device contaminated during manufacture or shipping | 5 | 2.2% | 0.3% |
| Improper or incorrect procedure or method | 5 | 2.2% | 0.6% |
| Difficult to removethe device was hard to remove | 4 | 1.8% | 2.9% |
| Material deformation | 4 | 1.8% | 0.6% |
| Material puncture/hole | 4 | 1.8% | 0.9% |
| Material integrity problema problem with the device material | 3 | 1.3% | 0.8% |
| Nonstandard device | 3 | 1.3% | 0.3% |
FDA's device problem codes as entered on the report; one report can carry several. Generic codes such as "no apparent adverse event" are left out.
Patient problems coded
| Patient problem (FDA code) | Reports | Share |
|---|---|---|
| Appropriate clinical signs, symptoms and conditions term/code not available | 24 | 10.7% |
| Extravasation | 10 | 4.4% |
| Painpain, site not specified | 10 | 4.4% |
| Swelling/ edema | 7 | 3.1% |
| Injurya physical injury | 3 | 1.3% |
| Thrombosis/thrombus | 3 | 1.3% |
| Discomfortdiscomfort | 2 | 0.9% |
| Erythemaskin redness | 2 | 0.9% |
| Foreign body in patientpart of a device left in the patient | 2 | 0.9% |
| Device embedded in tissue or plaque | 1 | 0.4% |
| Fungal infectiona fungal infection | 1 | 0.4% |
| Hypersensitivity/allergic reaction | 1 | 0.4% |
| Neck painneck pain | 1 | 0.4% |
| No patient involvement | 1 | 0.4% |
| Perforation of vessels | 1 | 0.4% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Power Port isp M.R.I., 8Fr Groshong | Product code LJT | All MAUDE reports |
|---|---|---|---|
| Reports | 225 | 22,475 | 26,136,888 |
| Share of that pool | — | 1% | 0% |
| Classified as death, per 1,000 reports | 0 | 18 | 9 |
| Classified as injury | 24.4% | 57.7% | 36.2% |
| Classified as malfunction | 75.6% | 38.6% | 62.3% |
| Filed by the manufacturer | 100% | 83.8% | 94.9% |
Shares are of reports, not of devices in use. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data."
Other brands with product code LJT
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| PowerPort ClearVUE isp Implantable Port, ChronoFlex Single-Lumen, 8F | 1,327 | 656 | 4.7% |
| PowerPort isp M.R.I. Implantable Port, Groshong Single-Lumen, 8F | 1,043 | 211 | 1.3% |
| PowerPort M.R.I. Implantable Port, ChronoFlex Single-Lumen, 8F | 689 | 341 | 4.2% |
| PowerPort isp M.R.I. Implantable Port, ChronoFlex Single-Lumen, 8F | 669 | 350 | 4.6% |
| Lifeport Vascular Access System | 609 | 0 | 0.5% |
| PowerPort isp MRI 6F CHRONW/OS | 456 | 183 | 0% |
| Celsite | 452 | 51 | 0.9% |
| Unknown Port | 435 | 16 | 0.7% |
| Implanted Port | 400 | 368 | 4.3% |
| Smart Port CT | 332 | 192 | 4.2% |
| PowerPort ClearVUE Slim Implantable Port, ChronoFlex Single-Lumen, Kit, 8F | 295 | 164 | 5.4% |
| Unknown Power Port | 293 | 5 | 1.7% |
| PowerPort duo M.R.I. Implantable Port, ChronoFlex Dual-Lumen, 9.5F | 279 | 74 | 3.2% |
| PowerPort isp MRI 6CF Int w SP, ATT, SL | 277 | 140 | 0% |
| M.R.I. Implantable Port, Hickman Single-Lumen, 9.6F | 213 | 62 | 2.3% |
Ordered by report count for navigation only. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA also states that "common products may have a higher number of adverse events due to the higher total number of people using the product."
Questions about Power Port isp M.R.I., 8Fr Groshong reports
How many FDA reports name Power Port isp M.R.I., 8Fr Groshong?
225 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 36 in the latest 12 months.
What kinds of events are reported?
malfunction (75.6%) and injury (24.4%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fracture (64.4%), deformation due to compressive stress (37.8%), naturally worn (28%), fluid/blood leak (26.2%) and material separation (25.3%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (100%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Power Port isp M.R.I., 8Fr Groshong was at fault?
No. FDA states that "MDR data alone cannot be used to establish rates of events, evaluate a change in event rates over time or compare event rates between devices. The number of reports cannot be interpreted or used in isolation to reach conclusions about the existence, severity, or frequency of problems associated with devices." It adds that the reporting system "has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data." FDA adds that "a causal relationship cannot be established between product and reactions listed in a report."
How do I report a problem with a medical device?
Through FDA MedWatch (Form FDA 3500 for health professionals and consumers), or to the manufacturer. See the guide on how to report.
Where this comes from. Counts are built from the openFDA Device Adverse Event (MAUDE) bulk export released 28 Sep 2026, which holds reports FDA received through 31 Aug 2026. Brand, generic and manufacturer names are as written on the reports; product code names come from FDA's device classification. A report counts here when any device it lists carries this brand name after punctuation and capitalisation are normalised. No report narrative, lot number, patient detail or reporter identity is published. See the methodology and sources; FDA's record is authoritative, and corrections are handled within five working days.
Drug data (FAERS) through 30 Jun 2026; device data (MAUDE) through 31 Aug 2026. Not medical advice.