Manufacturer
285 recalls in our database name Baxter Healthcare Corporation as the manufacturing or recalling firm.
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.
Pending LLM rewrite. Source: FDA_DEVICE Z-0201-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0196-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0199-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0204-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2594-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2333-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2334-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2332-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2415-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0596-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2173-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2096-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2095-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2031-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2032-2025.
Baxter Healthcare is recalling 2.5V rechargeable batteries for Welch Allyn PocketScope handles due to potential short circuits that can cause excessive heat and user burns.
Baxter is recalling certain Novum IQ Syringe Pumps manufactured or repaired after July 4, 2023, due to a design issue that may falsely detect a syringe flange when none is loaded, causing the pump interface to become stuck or display a System Error 21502.
Baxter Healthcare is recalling Affinity 4 Birthing Beds due to improper crimps on actuator signal wires that could prevent the bed or foot section from lowering. The defect affects 164 units distributed worldwide.
Baxter Healthcare is recalling the Novum IQ LVP Infusion System because the device may deliver less medication than intended when using standby mode or after being powered off with the set loaded.
Baxter Healthcare Corporation is recalling Welch Allyn Life2000 Compressor units due to a cybersecurity vulnerability discovered during internal testing.
Baxter Healthcare Corporation is recalling the Welch Allyn Life2000 Ventilation system due to a cybersecurity vulnerability discovered through internal testing. The recall affects 4,881 units distributed worldwide.
Baxter Healthcare is recalling Welch Allyn CP150 Electrocardiographs worldwide due to reports of battery-related fires. The fires occurred when devices used non-approved, third-party aftermarket batteries.
Baxter Healthcare is recalling the Welch Allyn CONNEX Accessory Power Management Stand due to reports of battery-related fires caused by unapproved third-party batteries.
Baxter Healthcare is recalling Welch Allyn Connex Vital Signs Monitors because some units experienced battery-related fires caused by unapproved third-party after-market batteries.
Baxter Healthcare Corporation is recalling certain Welch Allyn Connex Vital Signs Monitors due to an undeclared natural rubber band in the packaging of reusable blood pressure cuffs. The undeclared rubber may pose an allergen risk to individuals with natural rubber latex sensitivity.