Manufacturer
3 recalls in our database name Baxa Corporation as the manufacturing or recalling firm.
Of the 3 recalls from Baxa Corporation 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.
Baxter Healthcare is voluntarily recalling one lot of Baxa Vial Adapters due to an incorrect expiry date.
Baxter Healthcare is recalling ExactaMix 1200 and 2400 compounders because a battery failure causes the internal clock to reset to midnight on December 31, 2010.
Baxa Corporation is recalling Repeater Pump models 095, 099, and 099R because the included Technical Manual contradicts the Operator Manual regarding multiple source container use.