AXIOM Artis dBA, Model Number 7555357
Class I - DangerousWhat Should You Do?
- Check if you have this product: Serial Numbers: 53181 53023 53167 53104 53067 53093 53162 53706 53058 53098 53253 53016 53188 53209 53223 53700 53017 53114 53063 53219 53033 53142 53116 53002 53086 53195 53165 53076 53064 53124 53176 53078 53111 53227 53202 53133 53140 53047 53710 53190 53180 53128 53185 53170 53187 53019 53141 53084 53074 53225 53215 53189 53056 53166 53149 53020 53096 53009 53147 53070 53049 53261 53122 53065 53031 53085 53026 53222 53090 53075 53256 53045 53057 53103 53182 53012 53022 53175 53194 53102 53109 53260 53043 53160 53117
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Siemens Medical Solutions USA, Inc
- Reason for Recall:
- A tolerance issue in the power supply of the generator control above a specific value may cause generator A100 failure. As a result, the X-ray tube will not be supplied with the required voltage and X-ray will not be possible. The issue occurs sporadically; however, it may occur during an on-going procedure.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
AXIOM Artis dBA, Model Number 7555357
Product Codes/Lot Numbers:
Serial Numbers: 53181 53023 53167 53104 53067 53093 53162 53706 53058 53098 53253 53016 53188 53209 53223 53700 53017 53114 53063 53219 53033 53142 53116 53002 53086 53195 53165 53076 53064 53124 53176 53078 53111 53227 53202 53133 53140 53047 53710 53190 53180 53128 53185 53170 53187 53019 53141 53084 53074 53225 53215 53189 53056 53166 53149 53020 53096 53009 53147 53070 53049 53261 53122 53065 53031 53085 53026 53222 53090 53075 53256 53045 53057 53103 53182 53012 53022 53175 53194 53102 53109 53260 53043 53160 53117
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2022-2019
Related Recalls
ARTIS Icono biplane, floor and ceiling.: ARTIS icono biplane Model 11327600. ARTIS icono ceiling Model 11328100. ARTIS icono floor Model 11327700. interventional fluoroscopic x-ray system
Siemens Medical Solutions USA
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.
ARTIS pheno, Model 10849000. interventional fluoroscopic x-ray system
Siemens Medical Solutions USA
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.
ARTIS Pheno VE30A and VE40A, Model 10849000
Siemens Medical Solutions USA
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.