Devices › Interventional fluoroscopic x-ray system
Device brand name · Interventional fluoroscopic x-ray system
Base Sys Bi70002000 O-Arm Sys O2: medical device reports filed with FDA
336 reports name it, 2018–2020. Manufacturer given most often on reports: Medtronic Navigation Littleton. Product code OWB.
- 336
- device reports naming the brand
- 0% of all MAUDE reports · about 43 a year
- 0
- reports, 12 months to August 2026
- 0 in the 12 months before
- 99.4%
- classified as malfunction
- 98.5% across the product code
- 0%
- classified as death, as reported
- 0 reports · not verified by FDA
336 medical device reports received by FDA name the brand "Base Sys Bi70002000 O-Arm Sys O2" (interventional fluoroscopic x-ray system); the manufacturer given most often on reports is Medtronic Navigation Littleton; received from October 2018 to August 2020. 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 (99.4%) and injury (0.6%); across all interventional fluoroscopic x-ray system reports (product code OWB) death is recorded in 0.2% and malfunction in 98.5%. Event type is the reporter's classification of the report, not a verified outcome.
The device problems coded most often are application program freezes or fails to launch (47.3%), noise, audible (10.4%) and positioning problem (10.1%). The patient problems coded most often are no patient involvement, radiation exposure, unintended and tissue damage. 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 Base Sys Bi70002000 O-Arm Sys O2 was received in the five years to August 2026; the latest was received in August 2020.
By year received
Event type and report source
Event type, as classified on the report
Who filed the report
Grey bar: all 50,356 reports carrying product code OWB. 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 |
|---|---|---|---|
| Application program freezes or fails to launch | 159 | 47.3% | 8.6% |
| Noise, audible | 35 | 10.4% | 1.6% |
| Positioning problem | 34 | 10.1% | 2.4% |
| Communication or transmission problemthe device could not communicate or transmit | 30 | 8.9% | 1.7% |
| Failure to power up | 21 | 6.3% | 1.9% |
| Device sensing problem | 18 | 5.4% | 1.3% |
| Failure to charge | 14 | 4.2% | 0.3% |
| Failure to run on battery | 14 | 4.2% | 0.5% |
| Wireless communication problema wireless connection problem | 13 | 3.9% | 0.2% |
| Poor quality image | 8 | 2.4% | 1.2% |
| Calibration problem | 6 | 1.8% | 0.5% |
| Image display error/artifact | 6 | 1.8% | 0.7% |
| Imprecision | 6 | 1.8% | 0.5% |
| Material deformation | 6 | 1.8% | 0.5% |
| Power problem | 5 | 1.5% | 0.3% |
| Physical resistance/sticking | 4 | 1.2% | 0.3% |
| Device damaged prior to usethe device was damaged before use | 3 | 0.9% | 0.1% |
| Unexpected shutdown | 3 | 0.9% | 0.7% |
| No display/image | 2 | 0.6% | 4.3% |
| Unintended movement | 1 | 0.3% | 0.4% |
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 |
|---|---|---|
| No patient involvement | 213 | 63.4% |
| Radiation exposure, unintended | 3 | 0.9% |
| Tissue damage | 2 | 0.6% |
| Iatrogenic source | 1 | 0.3% |
| Staphylococcus aureus | 1 | 0.3% |
Patient problem codes are present mainly in reports filed since 2019 and are often blank.
In context
| Measure | Base Sys Bi70002000 O-Arm Sys O2 | Product code OWB | All MAUDE reports |
|---|---|---|---|
| Reports | 336 | 50,356 | 26,136,888 |
| Share of that pool | — | 0.7% | 0% |
| Classified as death, per 1,000 reports | 0 | 2 | 9 |
| Classified as injury | 0.6% | 1.2% | 36.2% |
| Classified as malfunction | 99.4% | 98.5% | 62.3% |
| Filed by the manufacturer | 100% | 99.6% | 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 OWB
| Brand | Reports | Latest 12 months | Classified as death |
|---|---|---|---|
| Allura Xper FD | 20,061 | 5,580 | 0.1% |
| Azurion | 10,988 | 3,673 | 0.1% |
| O-Arm O2 Imaging System | 10,979 | 681 | 0.1% |
| Allura Xper FD20 | 2,179 | 676 | 0.6% |
| Allura Xper FD20/10 & Allura Xper FD20/20 | 400 | 130 | 0.3% |
| O2 | 352 | 0 | 0.3% |
| Artis zee floor | 232 | 6 | 3.4% |
| Artis Zee Ceiling | 209 | 4 | 0.5% |
| O2 O-Arm Imaging System | 154 | 0 | 0% |
| O-Arm | 386 | 0 | 0% |
| Artis zee biplane | 182 | 7 | 1.1% |
| Allura Xper FD10/10 | 327 | 111 | 0.3% |
| O-Arm Imaging System | 396 | 44 | 1.5% |
| Allura Xper FD10 | 1,328 | 404 | 1.3% |
| Innova | 868 | 32 | 0.7% |
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 Base Sys Bi70002000 O-Arm Sys O2 reports
How many FDA reports name Base Sys Bi70002000 O-Arm Sys O2?
336 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 (99.4%) and injury (0.6%). "Event type" is how the report was classified when filed: death, injury, malfunction or other.
What device problems are coded?
application program freezes or fails to launch (47.3%), noise, audible (10.4%), positioning problem (10.1%), communication or transmission problem (8.9%) and failure to power up (6.3%). 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 Base Sys Bi70002000 O-Arm Sys O2 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.