Device manufacturer, as written on reports

Icu Medical Costa Rica: medical device reports filed with FDA

4,594 reports name it as the manufacturer of the device involved, 2018–2026.

Read first · FDA's statement on these data

Adverse event reports submitted to FDA do not undergo extensive validation or verification. Therefore, a causal relationship cannot be established between product and reactions listed in a report. While a suspected relationship may exist, it is not medically validated and should not be the sole source of information for clinical decision making or other assumptions about the safety or efficacy of a product. Additionally, it is important to remember that adverse event reports represent a small percentage of total usage numbers of a product. Common products may have a higher number of adverse events due to the higher total number of people using the product. openFDA, FDA

FDA adds: "Although MDRs are a valuable source of information, this passive surveillance system has limitations, including the potential submission of incomplete, inaccurate, untimely, unverified, or biased data. In addition, the incidence or prevalence of an event cannot be determined from this reporting system alone due to potential under-reporting of events and lack of information about frequency of device use." And: "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."

Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated.

Not medical advice. This site counts what was reported to FDA. Questions about a medicine or device belong with a pharmacist or clinician.

4,594
reports naming it as manufacturer: 0% of all MAUDE reports; 1,130
reports, 12 months to August 2026: 693 in the 12 months before; 96.1%
classified as malfunction: 62.3% across all reports; 1%
classified as death, as reported: 0.9% across all reports

4,594 medical device reports received by FDA give Icu Medical Costa Rica as the manufacturer of the device involved, 0% of the MAUDE database, from November 2018 to August 2026. Manufacturer names are as written on the report; subsidiaries and spelling variants may appear as separate names.

1,130 reports arrived in the 12 months to August 2026, up 63% from 693 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 (96.1%), injury (2.9%) and death (1%). Manufacturers are required to report events they learn of, so a large manufacturer with many products in use files many reports. 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."

Brands named most often

Brand	Device type	Reports	Latest 12 months	Classified as death
Primary PLUM Set, CLAVE Secondary Port, CLAVE Y-Site, Secure Lock, 103 Inch	Set, administration, intravascular	554	161	0.4%
PLUM 360 Infuser	Pump, infusion	504	79	3.2%
Plum 360 Driver New	Pump, infusion	255	20	1.6%
PLUM 150 mL Burette Set, CLAVE Injection Site, 2 CLAVE Y-Sites, SL, 114in	Set, administration, intravascular	204	48	0%
Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, CLAVE	Set, administration, intravascular	192	56	0.5%
Ls Pri Plum 15 Micron Cl 0 2m Pe 272cm	Set, administration, intravascular	159	0	0%
Plma Dvc V11 51 1 N	Pump, infusion	9	0	0%

Brands with a page on this site, 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."

Device types

Product code	Device type	Reports	Share
FPA	Set, administration, intravascular	2,912	63.4%
FRN	Pump, infusion	1,552	33.8%
KPE	Container, i.v.	53	1.2%
MRZ	Accessories, pump, infusion	26	0.6%
GBX	Catheter, irrigation	23	0.5%
MEA	Pump, infusion, pca	19	0.4%
DXQ	Blood pressure cuff	2	0%
FMG	Stopcock, i.v. set	2	0%
FPK	Tubing, fluid delivery	2	0%
ONB	Closed antineoplastic and hazardous drug reconstitution and transfer system	2	0%

Reports by month, five years

FDA releases MAUDE data monthly; reports can arrive months after an event, so the newest months grow in later releases.

Event type

Death1%46

Injury2.9%133

Malfunction96.1%4,413

Other0%2

Not given0%0

Grey bar: all 26,136,888 MAUDE reports. Event type is the filer's classification and is not verified by FDA.

Questions about Icu Medical Costa Rica reports

How many FDA device reports name Icu Medical Costa Rica as manufacturer?

4,594 reports through August 2026, 1,130 of them in the latest 12 months.

Which of its brands appear most often?

Primary PLUM Set, CLAVE Secondary Port, CLAVE Y-Site, Secure Lock, 103 Inch (554), PLUM 360 Infuser (504), Plum 360 Driver New (255), PLUM 150 mL Burette Set, CLAVE Injection Site, 2 CLAVE Y-Sites, SL, 114in (204) and Primary PLUM Set, 15 Micron Filter in Sight Chamber, CLAVE Secondary Port, CLAVE (192).

Which device types does it report on?

set, administration, intravascular (63.4%), pump, infusion (33.8%), container, i.v. (1.2%) and accessories, pump, infusion (0.6%).

Does a high count say something about the manufacturer?

Not by itself. Manufacturers must file a report for every event they become aware of, so report volume follows the number 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."

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. Manufacturer names are pooled after company suffixes (Inc., LLC, GmbH and similar) are dropped; names that read as a person rather than an organisation are never published. 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.