Siemens Medical Solutions USA, Inc recalls ARTIS Pheno VE30A and VE40A, Model 10849000
See all recalls from Siemens Medical Solutions USA, Inc →Recalled Product
ARTIS Pheno VE30A and VE40A, Model 10849000
Hazard / Issue
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.
Issued by
FDA
Distribution: U.S. and O.U.S.
Lot/Code Info: UDI 04056869046877
✅ 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 VE30A and →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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