Manufacturer
4 recalls in our database name Sedecal S.A. as the manufacturing or recalling firm.
Of the 4 recalls from Sedecal S.A. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (25%) are Severe.
The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.
Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.
Sedecal S.A. is recalling 145 NOVA FA DR diagnostic radiography systems because installation or maintenance issues could cause support cables to break, leading to equipment falling.
Sedecal S.A. is recalling 349 mobile X-ray systems because static electricity and other issues can cause uncommanded movements.
Sedecal S.A. is recalling RadPro 40kW Digital X-Ray systems because electrostatic energy may cause uncontrolled movements that could bump into users or patients.
Sedecal S.A. is recalling 283 MobileDiagnost wDR motorized portable diagnostic X-ray systems due to reports of unexpected movement.