Intelli-C AccessoryRecalls & reported problems across all models
Nrt - Nordisk Røntgen Teknik A/S · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one Intelli-C Accessory model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of Intelli-C Accessory by Nrt - Nordisk Røntgen Teknik A/S in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jan 21, 2022 and Jan 21, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Slipped” (1 report).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Intelli-C Accessory recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- Jan 21, 2022Open, Classified
Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.
Z-0526-2022 · Root cause: Process control · names 2 of these models · Recall details · FDA record ↗
Most reported Intelli-C Accessory problems
Device problems
- Device Slipped1
Patient problems
- Insufficient Information1
Intelli-C Accessory models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Intelli-C Accessory 03282000Interventional Fluoroscopic X-Ray System1 recall1 report
- Intelli-C Accessory 03283000Interventional Fluoroscopic X-Ray System1 recall0 reports
Recent Intelli-C Accessory adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJan 21, 2022Device Slipped
IT WAS REPORTED THAT THE FOOTREST SLID DOWN ALONG THE PATIENT TABLE WHILE IN USE WITH A PATIENT. THE PATIENT GRABBED THE PATIENT TABLE AND DID NOT FALL.
Patient problems: Insufficient Information
MAUDE report 13318352 ↗
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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