Devices › System, hypothermia, intravenous, cooling
Device brand name · Central venous catheter
Zoll Ivtm Icy Catheter: medical device reports filed with FDA
429 reports name it, 2013–2024. Manufacturer given most often on reports: Zoll Circulation. Product code NCX.
- 429
- device reports naming the brand
- 0% of all MAUDE reports · about 33 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 90%
- classified as malfunction
- 92.9% across the product code
- 1.9%
- classified as death, as reported
- 8 reports · not verified by FDA
429 medical device reports received by FDA name the brand "Zoll Ivtm Icy Catheter" (central venous catheter); the manufacturer given most often on reports is Zoll Circulation; received from May 2013 to June 2024. Brand names are as the reporter or manufacturer wrote them, so one product can appear under several spellings.
0 reports arrived in the 12 months to August 2026, and none 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 (90%), injury (8.2%) and death (1.9%); across all system, hypothermia, intravenous, cooling reports (product code NCX) death is recorded in 1% and malfunction in 92.9%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are fluid/blood leak (50.6%), material integrity problem (49.9%) and leak/splash (19.6%). The patient problems coded most often are thrombosis/thrombus, cardiac arrest and thrombosis. 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 4,407 reports carrying product code NCX. 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 | 217 | 50.6% | 17.7% |
| Material integrity problema problem with the device material | 214 | 49.9% | 16.9% |
| Leak/splashthe device leaked | 84 | 19.6% | 5.5% |
| Device operates differently than expectedthe device behaved unexpectedly | 61 | 14.2% | 11.8% |
| Difficult to advance | 9 | 2.1% | 0.7% |
| Device issuea problem with the device | 7 | 1.6% | 3.2% |
| Difficult to removethe device was hard to remove | 5 | 1.2% | 1% |
| Difficult to insertthe device was hard to insert | 4 | 0.9% | 0.5% |
| Insufficient cooling | 4 | 0.9% | 1.8% |
| Temperature problem | 2 | 0.5% | 1.7% |
| Crackthe device cracked | 1 | 0.2% | 0% |
| Detachment of device or device componentpart of the device came off | 1 | 0.2% | 0.1% |
| Device operational issue | 1 | 0.2% | 1.2% |
| Failure to deflate | 1 | 0.2% | 0% |
| Infusion or flow problema problem with flow or infusion | 1 | 0.2% | 0% |
| Insufficient heating | 1 | 0.2% | 1% |
| Material twisted/bent | 1 | 0.2% | 0% |
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 |
|---|---|---|
| Thrombosis/thrombus | 8 | 1.9% |
| Cardiac arrestthe heart stopped | 7 | 1.6% |
| Thrombosis | 7 | 1.6% |
| Hemorrhage/blood loss/bleeding | 5 | 1.2% |
| Pulmonary embolisma blood clot in the lung | 3 | 0.7% |
| No patient involvement | 2 | 0.5% |
| Swelling/ edema | 2 | 0.5% |
| Thrombus | 2 | 0.5% |
| Abdominal painstomach or belly pain | 1 | 0.2% |
| Air embolism | 1 | 0.2% |
| Bacterial infectiona bacterial infection | 1 | 0.2% |
| Deaththe patient died; cause not stated by this term | 1 | 0.2% |
| Ecchymosis | 1 | 0.2% |
| Inflammationinflammation | 1 | 0.2% |
| Not applicable | 1 | 0.2% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Zoll Ivtm Icy Catheter | Product code NCX | All MAUDE reports |
|---|---|---|---|
| Reports | 429 | 4,407 | 26,136,888 |
| Share of that pool | — | 9.7% | 0% |
| Classified as death, per 1,000 reports | 19 | 10 | 9 |
| Classified as injury | 8.2% | 5.9% | 36.2% |
| Classified as malfunction | 90% | 92.9% | 62.3% |
| Filed by the manufacturer | 100% | 96.9% | 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 NCX
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Zoll Ivtm Thermogard Xp | 2,238 | 0 | 0.1% |
| Zoll Ivtm Quattro Catheter | 399 | 0 | 4.8% |
| Thermogard XP | 331 | 163 | 0% |
| Zoll Ivtm Solex 7 Catheter | 195 | 0 | 2.1% |
| Invisalign System | 534 | 0 | 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 Zoll Ivtm Icy Catheter reports
How many FDA reports name Zoll Ivtm Icy Catheter?
429 medical device reports in the openFDA MAUDE release of 28 Sep 2026, covering reports received through August 2026; 0 in the latest 12 months.
What kinds of events are reported?
malfunction (90%), injury (8.2%) and death (1.9%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
fluid/blood leak (50.6%), material integrity problem (49.9%), leak/splash (19.6%), device operates differently than expected (14.2%) and difficult to advance (2.1%). 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 Zoll Ivtm Icy Catheter 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.