Siemens Medical Solutions USA, Inc recalls ARTIS pheno, Model 10849000. interventional fluoroscopic x-r
See all recalls from Siemens Medical Solutions USA, Inc →Recalled Product
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
Hazard / Issue
During patient examinations, the system may sporadically display a 0 x-ray dose administered to the patient. This behavior has only been observed during fluoroscopy and/or single-frame acquisitions. Despite the reported x-ray dose showing 0, an actual x-ray dose is applied to the patient.
Issued by
FDA
Distribution: US and Worldwide
Lot/Code Info: UDI: 4056869046877
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for ARTIS pheno, Model 10849000. →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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