Image-intensified fluoroscopic x-ray system, mobile: medical device reports filed with FDA

10,994 reports carry this product code, 2012–2026; 10 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.

10,994
reports with this product code: 0% of all MAUDE reports; 65
reports, 12 months to August 2026: 155 in the 12 months before; 97.2%
classified as malfunction: 62.3% across all reports; 0.1%
classified as death, as reported: 0.9% across all reports

Product code OXO is FDA's classification for "Image-intensified fluoroscopic x-ray system, mobile" (radiology panel), a class 2 device. 10,994 medical device reports carry this product code, 0% of the MAUDE database, from August 2012 to August 2026.

65 reports arrived in the 12 months to August 2026, down 58% from 155 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%), injury (2.6%) and death (0.1%). 10 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
O-Arm 1000 Imaging System	7,003	2	0%	98.6%
O-Arm 1000 Imaging System 3rd Edition	2,612	4	0%	99.1%
O-Arm Imaging System	354	44	1.5%	63.9%
O-Arm	251	0	0%	98.7%
Medtronic Navigation	19	69	6.7%	30.4%
O-Arm O2 Imaging System	3	681	0.1%	99%
C-Arm	1	4	0%	98.5%
Cart 9734056 S7 Staff Shrt 100-120v Intl	1	4	0%	95.1%
Stealthstation	1	0	0%	97.9%
Stenoscop	1	0	0%	100%

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
Medtronic Navigation Littleton	10,640	96.8%
Medtronic Navigation	109	1%
Siemens Healthcare	25	0.2%
Medtronic Navigation Louisville	19	0.2%
Ge Oec Medical Systems	6	0.1%
Sanmina -Sci Systems	6	0.1%
Hologic	5	0%
Philips Healthcare	2	0%
Philips Medical Systems Nederland	2	0%
Ge Medical Systems	1	0%
Ge Oec Medical Systems Slc	1	0%
Medtronic Cryocath	1	0%
Siemens Medical Solutions USA	1	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 and report source

Event type

Death0.1%8

Injury2.6%287

Malfunction97.2%10,687

Other0%5

Not given0.1%7

Who filed

Manufacturer report99.6%10,951

Voluntary report0.2%21

User facility report0%0

Distributor report0%0

Not given0.2%22

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

Device problems coded

Device problem (FDA code)	Reports	Share
Device operates differently than expectedthe device behaved unexpectedly	3,479	31.6%
Electrical /electronic property probleman electrical or electronic problem	1,835	16.7%
Application program freezes or fails to launch	1,769	16.1%
Device displays incorrect message	1,169	10.6%
Communication or transmission problemthe device could not communicate or transmit	1,092	9.9%
Device inoperablethe device could not be used	1,085	9.9%
Computer software problema software problem	504	4.6%
Poor quality image	406	3.7%
Difficult to open or close	386	3.5%
Positioning problem	383	3.5%
Mechanical problema mechanical problem	362	3.3%
Unexpected shutdown	270	2.5%
Device stops intermittentlythe device stopped now and then	258	2.3%
Failure to run on battery	255	2.3%
Material deformation	253	2.3%
Application interface becomes non-functional or program exits abnormally	241	2.2%
Failure to power up	240	2.2%
Imprecision	231	2.1%
Noise, audible	201	1.8%
Display or visual feedback problem	200	1.8%

Questions about image-intensified fluoroscopic x-ray system, mobile reports

What is product code OXO?

FDA's classification code for "Image-intensified fluoroscopic x-ray system, mobile", class 2, reviewed by the radiology panel. Every device report carries the product code of the device involved.

How many reports carry this code?

10,994 reports through August 2026, 65 of them in the latest 12 months.

Which brands appear most often?

O-Arm 1000 Imaging System (7,003), O-Arm 1000 Imaging System 3rd Edition (2,612), O-Arm Imaging System (354), O-Arm (251) and Medtronic Navigation (19). 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.