Manufacturer
5 recalls in our database name Moller Vital as the manufacturing or recalling firm.
Of the 5 recalls from Moller Vital we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3 (60%) 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.
Moller Vital is recalling Molift 2-Point sling bars because broken hooks may cause the sling to slip and patients to fall.
Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.
Moller Vital is recalling Molift Air ceiling hoists because the suspension coupling bolt may come loose, posing a risk of patient falls.
Moller Vital is recalling 7,555 Molift Smart 150 units because the leg spreading mechanism may fail to hoist and collapse if assembled incorrectly.
Moller Vital is recalling 1,460 Molift Smart 150 patient lifts because the leg spreading mechanism may fail to hoist and collapse if assembled incorrectly.