Devices › Set, administration, intravascular
Device brand name · Set administration intravascular
Clearlink/Continu-Flo/Duo-Vent: medical device reports filed with FDA
772 reports name it, 2017–2026. Manufacturer given most often on reports: Baxter Healthcare. Product code FPA.
- 772
- device reports naming the brand
- 0% of all MAUDE reports · about 81 a year
- 282
- reports, 12 months to August 2026
- 330 in the 12 months before
- 97.2%
- classified as malfunction
- 79.3% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
772 medical device reports received by FDA name the brand "Clearlink/Continu-Flo/Duo-Vent" (set administration intravascular); the manufacturer given most often on reports is Baxter Healthcare; received from January 2017 to August 2026. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
282 reports arrived in the 12 months to August 2026, down 15% from 330 in 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 (97.2%) and injury (2.7%); across all set, administration, intravascular reports (product code FPA) death is recorded in 0.2% and malfunction in 79.3%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are fluid/blood leak (54.4%), detachment of device or device component (16.3%) and break (6.1%). The patient problems coded most often are low blood pressure/ hypotension, appropriate clinical signs, symptoms and conditions term/code not available and chemical exposure. 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 349,387 reports carrying product code FPA. 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 |
|---|---|---|---|
| Fluid/blood leak | 420 | 54.4% | 13.5% |
| Detachment of device or device componentpart of the device came off | 126 | 16.3% | 3.9% |
| Breakthe device broke | 47 | 6.1% | 2.1% |
| Material puncture/hole | 40 | 5.2% | 0.3% |
| Backflow | 36 | 4.7% | 0.5% |
| Material split, cut or torn | 31 | 4% | 0.2% |
| Disconnection | 22 | 2.8% | 1.8% |
| Air/gas in device | 21 | 2.7% | 0.9% |
| Crackthe device cracked | 21 | 2.7% | 1.5% |
| Leak/splashthe device leaked | 21 | 2.7% | 11.2% |
| Material twisted/bent | 11 | 1.4% | 12.2% |
| Device contamination with chemical or other material | 9 | 1.2% | 0.5% |
| No flow | 9 | 1.2% | 1% |
| Component misassembled | 6 | 0.8% | 0% |
| Component missing | 5 | 0.6% | 0.2% |
| Fitting problem | 5 | 0.6% | 0.1% |
| Connection problema connection problem | 4 | 0.5% | 0.5% |
| Incomplete or inadequate connection | 4 | 0.5% | 0.1% |
| Defective devicethe device was defective | 3 | 0.4% | 0.2% |
| Obstruction of flow | 3 | 0.4% | 0.7% |
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 |
|---|---|---|
| Low blood pressure/ hypotension | 8 | 1% |
| Appropriate clinical signs, symptoms and conditions term/code not available | 5 | 0.6% |
| Chemical exposure | 5 | 0.6% |
| Hemorrhage/blood loss/bleeding | 5 | 0.6% |
| Air embolism | 4 | 0.5% |
| Dyspneashortness of breath | 3 | 0.4% |
| Tachycardiafast heart rate | 3 | 0.4% |
| Decreased respiratory rate | 2 | 0.3% |
| Epilepsy | 1 | 0.1% |
| Fever | 1 | 0.1% |
| Foreign body in patientpart of a device left in the patient | 1 | 0.1% |
| High blood pressure/ hypertension | 1 | 0.1% |
| Increased respiratory rate | 1 | 0.1% |
| Obstruction/occlusion | 1 | 0.1% |
| Reaction to medicinal component of device | 1 | 0.1% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Clearlink/Continu-Flo/Duo-Vent | Product code FPA | All MAUDE reports |
|---|---|---|---|
| Reports | 772 | 349,387 | 26,136,888 |
| Share of that pool | — | 0.2% | 0% |
| Classified as death, per 1,000 reports | 0 | 2 | 9 |
| Classified as injury | 2.7% | 20% | 36.2% |
| Classified as malfunction | 97.2% | 79.3% | 62.3% |
| Filed by the manufacturer | 78.6% | 96.3% | 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 FPA
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Inset Guard | 47,276 | 47,222 | 0.1% |
| Inset | 26,405 | 25,656 | 0% |
| Quick Set | 23,351 | 23,028 | 0.4% |
| Autosoft Xc | 20,328 | 49 | 0% |
| Autosoft 90 | 12,143 | 15 | 0% |
| Access | 14,160 | 0 | 0% |
| Other Accessories | 10,429 | 10,425 | 1.7% |
| Alaris Pump Module Administration Set | 8,492 | 0 | 0.2% |
| Contact Detach | 6,473 | 6,157 | 0.1% |
| Inset 30 | 3,528 | 3,461 | 0% |
| Cadd | 10,811 | 9 | 0.1% |
| Minimed Quick-Set | 3,101 | 6 | 0% |
| Cleo 90 Infusion Set | 3,006 | 23 | 0% |
| Trusteel | 2,886 | 14 | 0% |
| Autosoft 30 | 2,374 | 1 | 0% |
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 Clearlink/Continu-Flo/Duo-Vent reports
How many FDA reports name Clearlink/Continu-Flo/Duo-Vent?
772 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 282 in the latest 12 months.
What kinds of events are reported?
malfunction (97.2%) and injury (2.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fluid/blood leak (54.4%), detachment of device or device component (16.3%), break (6.1%), material puncture/hole (5.2%) and backflow (4.7%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (78.6%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Clearlink/Continu-Flo/Duo-Vent 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.