Enteroscope and accessories: medical device reports filed with FDA

825 reports carry this product code, 2002–2026; 8 brands with a page.

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.

825
reports with this product code: 0% of all MAUDE reports; 259
reports, 12 months to August 2026: 79 in the 12 months before; 57.8%
classified as malfunction: 62.3% across all reports; 1.2%
classified as death, as reported: 0.9% across all reports

Product code FDA is FDA's classification for "Enteroscope and accessories" (gastroenterology, Urology panel), a class 2 device. 825 medical device reports carry this product code, 0% of the MAUDE database, from May 2002 to August 2026.

259 reports arrived in the 12 months to August 2026, up 228% from 79 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 (57.8%), injury (40.2%) and death (1.2%). 8 brand names with a page on this site carry this code; the brands table is 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."

Brands with this product code

Brand	Reports	Latest 12 months	Classified as death	Classified as malfunction
Evis Lucera Small Intestinal Videoscope	153	43	0%	47.7%
Other Accessories	18	10,425	1.7%	49.1%
8100 Alaris Pump Module	7	0	0%	100%
Inset Guard	5	47,222	0.1%	73.1%
8110 Alaris Syringe Pump	1	0	0%	100%
8300 Alaris Etco2 Module	1	0	0%	100%
CADD Extension Set	1	177	0.1%	96.8%
Motiva Implants	1	1,729	0%	4.6%

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."

Manufacturers named

Manufacturer (as written on reports)	Reports	Share
Aizu Olympus	420	50.9%
Olympus Medical Systems	75	9.1%
Unomedical Devices De C V	15	1.8%
Unomedical A/S	10	1.2%
Carefusion Sd	9	1.1%
Olympus Optical	3	0.4%
Given Imaging	2	0.2%
Establishment Labs	1	0.1%
Olympus Medical System	1	0.1%

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 and report source

Event type

Death1.2%10

Injury40.2%332

Malfunction57.8%477

Other0.4%3

Not given0.4%3

Who filed

Manufacturer report96.7%798

Voluntary report0.5%4

User facility report0%0

Distributor report2.3%19

Not given0.5%4

Grey bar: all 26,136,888 MAUDE reports.

Device problems coded

Device problem (FDA code)	Reports	Share
Failure to clean adequately	165	20%
Microbial contamination of device	46	5.6%
Insufficient device problem information	36	4.4%
Device reprocessing problem	34	4.1%
Poor quality image	27	3.3%
No display/image	25	3%
Contamination	16	1.9%
Erratic or intermittent display	16	1.9%
Residue after decontamination	14	1.7%
Melted	13	1.6%
Loss of or failure to bond	12	1.5%
Premature separation	12	1.5%
Corrodedthe device corroded	11	1.3%
Pressure problem	11	1.3%
Device operates differently than expectedthe device behaved unexpectedly	10	1.2%
Inflation problem	8	1%
Mechanical problema mechanical problem	7	0.8%
Thermal decomposition of device	7	0.8%
Use of incorrect control/treatment settings	7	0.8%
Detachment of device or device componentpart of the device came off	6	0.7%

Questions about enteroscope and accessories reports

What is product code FDA?

FDA's classification code for "Enteroscope and accessories", class 2, reviewed by the gastroenterology, Urology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

825 reports through August 2026, 259 of them in the latest 12 months.

Which brands appear most often?

Evis Lucera Small Intestinal Videoscope (153), Other Accessories (18), 8100 Alaris Pump Module (7), Inset Guard (5) and 8110 Alaris Syringe Pump (1). Widely used products collect more reports because more people use them.

Can the brands table be used to rank the devices?

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." Brands differ in how many are in use, how long they have been sold and how reports are collected.

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. 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.