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All product recalls associated with Siemens AG/Siemens Healthcare GmbH Rittigfeld 1 Forchheim Germany.
Total Recalls
1000
Past Year
620
Class I (Serious)
91
Most Recent
Dec 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
A potential issue with ARTIS icono systems equipped with a small detector and a corresponding collimator (model # 10843101) was identified. In very rare situations, the first x-ray release following patient registration may be performed with incorrect copper prefiltration. If the described issue occurs, the applied radiation dose rate may be higher than intended by the user.
The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
Catheters may contain a hole in the catheter tubing, which could result in leakage during the insertion process.