Manufacturer
1 recall in our database name ZIEHM-ORTHOSCAN INC as the manufacturing or recalling firm.
Of the 1 recalls from ZIEHM-ORTHOSCAN 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.
Ziehm-Orthoscan is recalling 55 Orthoscan VERSA Accessory Carts and Versa Mini C-Arm Systems because a weld defect may cause the monitor arm to separate from the cart.