Devices › Catheter, intravascular, therapeutic, short-term less than 30 days
Device brand name · Injection site
Interlink Injection Site: medical device reports filed with FDA
150 reports name it, 1994–2009. Manufacturer given most often on reports: Baxter Healthcare Pte. Product code FOZ.
- 150
- device reports naming the brand
- 0% of all MAUDE reports · about 5 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 92%
- classified as malfunction
- 83.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
FDA's MAUDE database holds 150 reports that name the brand "Interlink Injection Site" (injection site), received between January 1994 and September 2009; the manufacturer given most often on reports is Baxter Healthcare Pte. Spellings of one product vary from report to report.
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 (92%), injury (6%) and other (0.7%); across all catheter, intravascular, therapeutic, short-term less than 30 days reports (product code FOZ) death is recorded in 0.3% and malfunction in 83.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are dislodged (29.3%), leak/splash (15.3%) and other (for use when an appropriate device code cannot be identified) (11.3%). The patient problems coded most often are bleeding, exposure to body fluids and therapy/non-surgical treatment, additional. 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
No report naming Interlink Injection Site was received in the five years to August 2026; the latest was received in September 2009.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 49,301 reports carrying product code FOZ. 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 |
|---|---|---|---|
| Dislodged | 44 | 29.3% | 0.2% |
| Leak/splashthe device leaked | 23 | 15.3% | 21.4% |
| Other (for use when an appropriate device code cannot be identified) | 17 | 11.3% | 0.3% |
| Detachment of device component | 13 | 8.7% | 1.6% |
| Material separation | 12 | 8% | 4.2% |
| Replace | 11 | 7.3% | 0.8% |
| Loose | 10 | 6.7% | 0.1% |
| Crackthe device cracked | 9 | 6% | 2.1% |
| Misassembled | 9 | 6% | 0.1% |
| Breakthe device broke | 4 | 2.7% | 10.9% |
| Disconnection | 4 | 2.7% | 0.7% |
| Burst container or vessel | 3 | 2% | 0.1% |
| Contamination | 3 | 2% | 1% |
| Displacement | 3 | 2% | 0% |
| Fluid/blood leak | 3 | 2% | 6.7% |
| Loose or intermittent connection | 3 | 2% | 0.4% |
| Material rupture | 3 | 2% | 0.5% |
| Backflow | 2 | 1.3% | 0.2% |
| Component(s), broken | 2 | 1.3% | 0.2% |
| Design/structure problem | 2 | 1.3% | 0.1% |
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 |
|---|---|---|
| Bleeding | 17 | 11.3% |
| Exposure to body fluids | 10 | 6.7% |
| Therapy/non-surgical treatment, additional | 7 | 4.7% |
| Treatment with medication(s) | 3 | 2% |
| Blood loss | 2 | 1.3% |
| Allergic reactionan allergic reaction | 1 | 0.7% |
| Confusion/ disorientation | 1 | 0.7% |
| Contamination, chemical | 1 | 0.7% |
| Cramp(s) | 1 | 0.7% |
| Dizzinesslight-headedness or unsteadiness | 1 | 0.7% |
| Foreign body, removal of | 1 | 0.7% |
| Inflammationinflammation | 1 | 0.7% |
| Missed dose | 1 | 0.7% |
| Other (for use when an appropriate patient code cannot be identified) | 1 | 0.7% |
| Surgical procedure | 1 | 0.7% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Interlink Injection Site | Product code FOZ | All MAUDE reports |
|---|---|---|---|
| Reports | 150 | 49,301 | 26,136,888 |
| Share of that pool | — | 0.3% | 0% |
| Classified as death, per 1,000 reports | 0 | 3 | 9 |
| Classified as injury | 6% | 13.1% | 36.2% |
| Classified as malfunction | 92% | 83.5% | 62.3% |
| Filed by the manufacturer | 93.3% | 89.6% | 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 FOZ
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Insyte AUTOGUARD | 1,314 | 1,050 | 0% |
| BD Insyte Autoguard | 1,246 | 55 | 0% |
| Introcan Safety | 1,255 | 45 | 0.1% |
| Bd Insyte Autog Bc | 695 | 0 | 0% |
| Arrow Cvc Set 3-Lumen 7 Fr X 20 Cm | 1,110 | 123 | 0.1% |
| Arrow Cvc Set 2-Lumen 7 Fr X 20 Cm | 1,406 | 170 | 0.1% |
| Nexiva | 385 | 304 | 0% |
| Mahurkar | 1,046 | 6 | 1.1% |
| BD Nexiva | 372 | 14 | 0% |
| Jelco | 363 | 34 | 0% |
| Arrow Pi Cvc Kit 3-L 7 Fr X 20 Cm Agb | 286 | 63 | 1% |
| Arrow Cvc Set 16 Ga X 8 20 Cm | 551 | 0 | 0% |
| Arrow Cvc Set 3-Lumen 7 Fr X 30 Cm | 338 | 12 | 0% |
| Bd Nexiva Single Port | 224 | 0 | 0% |
| Unspecified Bd Catheter | 251 | 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 Interlink Injection Site reports
How many FDA reports name Interlink Injection Site?
150 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 (92%), injury (6%) and other (0.7%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
dislodged (29.3%), leak/splash (15.3%), other (for use when an appropriate device code cannot be identified) (11.3%), detachment of device component (8.7%) and material separation (8%). These are FDA's device problem codes as entered on the report.
Who files these reports?
manufacturer reports (93.3%) and voluntary reports (6.7%). Manufacturers and user facilities are required to report; voluntary reports come from health professionals and the public.
Do these reports show that Interlink Injection Site 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.