Manufacturer
5 recalls in our database name Salter Labs as the manufacturing or recalling firm.
Of the 5 recalls from Salter Labs 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.
Salter Labs is recalling 70 T-piece Nebulizers because the T-piece does not fit on the nebulizer. The devices were distributed in six US states and China.
Salter Labs is recalling specific NebuTech nebulizer models because the inspiratory valve cap may detach during treatment.
Salter Labs is recalling 584 units of Model No. 8120-7 oxygen masks because the insert label incorrectly identifies the device as a non-rebreather instead of a partial rebreather.
Salter Labs is recalling specific lots of 15-foot CO2 sample lines because they may contain 30-foot tubes instead.
Salter Labs is recalling 242 cases of adult divided cannulas because some units labeled with male luer lock connectors actually contained female luer lock connectors.