Manufacturer
33 recalls in our database name Philips Medical Systems Gmbh, DMC as the manufacturing or recalling firm.
Of the 33 recalls from Philips Medical Systems Gmbh, DMC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 4 (12%) 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.
Philips is recalling DigitalDiagnost 4.1 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost 4.1 units because a defective hook allows the footplate to fall, posing a risk of injury to patients or operators.
Philips is recalling DigitalDiagnost 4 High Performance units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Single Detector units because a defective hook allows the footplate to fall or swing, posing a risk of injury to patients or operators.
Philips is recalling DigitalDiagnost Dual-Detector units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling BuckyDiagnost Ceiling Systems because the footplate hook may fail to hold the plate securely, posing a risk of injury to patients or operators.
Philips is recalling DigitalDiagnost Classic units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.
Philips is recalling DigitalDiagnost Single-Detect units because a defective hook allows the footplate to fall or swing, posing an injury risk to patients and operators.