Manufacturer
3 recalls in our database name Vilex In Tennessee Inc as the manufacturing or recalling firm.
Of the 3 recalls from Vilex In Tennessee 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.
Vilex, Inc. is recalling 4 units of FUZE 10.0 mm x 250 mm ankle arthrodesis screws due to a higher-than-expected incidence of breakage.
Vilex, Inc. is recalling 13 units of FUZE 10.0 mm x 150 mm ankle arthrodesis screws because the incidence of breakage is higher than expected.
Vilex, Inc. is recalling FUZE 10.0 mm x 200 mm ankle arthrodesis screws because the incidence of breakage is higher than expected.