Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of General ElectricLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list General Electric Med Systems LLC with 3 device recalls. The most recent is a device recall dated May 31, 2006: GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188….
| May 31, 2006 | GE Healthcare Revolution XR/d; GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model numbers: 2259988-2 & 2351505. The RevolutClass II · An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Pr | Device recalls |
| May 31, 2006 | GE Healthcare Definium 8000 Digital Radiographic Systems : GE Healthcare, 3000 North Grandview , Waukesha, WI, 53188 Model Number: 513107Class II · An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Pr | Device recalls |
| May 31, 2006 | GE Proteus XR/a Radiographic System. GE Medical Systems-Americas Milwaukee, WI. Model Number: 2259988. Product is indicated for use in Class II · An incident was reported that an operator's finger was pinched between the fixed roller and the gliding tabletop of a Pr | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
