Cios SelectRecalls & reported problems across all models
Siemens Shanghai Medical Equipment Ltd. · 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 Cios Select 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 Cios Select by Siemens Shanghai Medical Equipment Ltd. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Nov 22, 2023 and Nov 22, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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
Reports received per month, all models
Cios Select 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.
- Jun 5, 2023Open, Classified
Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of liquid following the plexiglass dropping off, at the same time the user or operator happens to touch the liquid on the cover which is connected to the internal live parts).
Z-2240-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Most reported Cios Select problems
Device problems
- Improper or Incorrect Procedure or Method1
- Use of Device Problem1
Patient problems
- Bone Fracture(s)1
Cios Select models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Cios Select 11020806Interventional fluoroscopic x-ray system1 recall0 reports
- Cios Select 10893686Image-intensified fluoroscopic x-ray system, mobile1 report
Recent Cios Select adverse event reports
The 1 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2023Use of Device Problem; Improper or Incorrect Procedure or Method; Use of Device Problem; Improper or Incorrect Procedure or Method
IT WAS REPORTED TO SIEMENS THAT AN ADVERSE EVENT OCCURRED WHILE OPERATING THE CIOS SELECT SYSTEM. DURING A PROCEDURE, WHILE THE DOCTOR WAS ROTATING THE C-ARM, THE TECHNICIAN GRABBED ROTATING PARTS OF THE C-ARM, RESULTING IN A DISTAL PHALANX FRACTURE. THERE IS NO REPORT OF IMPACT TO ANY PATIENT INVOLVED.
Patient problems: Bone Fracture(s)
MAUDE report 18189748 ↗
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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