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 Siemens HealthineersLabelled 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 Leibel-Flarsheim Company with 1 device recall. The most recent is a device recall dated Apr 25, 2013: Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem Company. The Sy….
| Date | Record | Source |
|---|---|---|
| Apr 25, 2013 | Hydra Vision DR 60/80 System, Models 700539 and 700540, Liebel-Flarshiem Company. The System is used in radiologic imaging procedures.Class II · A complaint was received in which a hospital physicist indicated the dosage was too high on the HUT system. During the s | 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
