Manufacturer
3 recalls in our database name Suntech Medical, Inc. as the manufacturing or recalling firm.
Of the 3 recalls from Suntech Medical, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) 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.
Suntech Medical is recalling Oscar 2 blood pressure monitors because the display may show an incorrect decimal point for three-digit readings in mmHg.
Suntech Medical is recalling 384 Model 250D Ambulatory Blood Pressure Monitors due to a user safety issue involving the misuse of rechargeable batteries.
Suntech Medical is recalling 80 neonate blood pressure cuffs because size #3 cuffs were packaged with size #4 labels.