Manufacturer
29 recalls in our database name Ossur H / F as the manufacturing or recalling firm.
Of the 29 recalls from Ossur H / F we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1 (3%) 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.
Ossur Americas is recalling various medical devices, including knee braces and walkers, due to unspecified product issues.
Ossur Americas is recalling various medical devices, including knee shields and walkers, because the packaging is defective.
Ossur is recalling two Rheo Knee bionic prosthetic units because they were released for distribution without completing the full assembly process.
Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.