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 BayerLabelled 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. See the Bayer group view.
As of Nov 14, 2026, FDA's public records list Medrad MR with 1 device recall. The most recent is a device recall dated Nov 21, 2013: Medrad Veris MR Monitor units The system is intended to monitor physiological parame….
| Date | Record | Source |
|---|---|---|
| Nov 21, 2013 | Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. Class II · The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected 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
