Manufacturer
279 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.
Baxter Healthcare recalls Novum IQ infusion pumps due to software anomalies that may cause blank display screens or false motor movement alerts. 43,922 units affected.
Baxter Healthcare is issuing an urgent correction for the Novum IQ Syringe Pump due to software anomalies that may display a blank run screen or generate false motor movement errors. The correction affects 10,101 units distributed in the US, Puerto Rico, and Canada.
Baxter is recalling six Spectrum IQ Infusion Pumps distributed to Arizona and Florida due to potential grease breakdown in the motor mechanism, which could result in excessive medication delivery.
Baxter Healthcare Corporation is voluntarily recalling acetaminophen injection due to discoloration observed in the product. The recall affects 13,000 containers distributed nationwide.
Baxter Novum IQ Large Volume Pumps may infuse medication at incorrect rates during flow-rate transitions or due to improper tubing loading. The 36,705 affected units worldwide should be checked per safety instructions.
Baxter Healthcare recalls 14 SIGMA Spectrum Infusion Pump V6 units due to incorrect software version. The recalled units were distributed to 10 US states.
Baxter Healthcare is recalling 28 SIGMA Spectrum Infusion Pump V8 units due to incorrect software versions. Affected facilities should contact Baxter immediately.
Hillrom LikoScale adapter kits for patient lifts have false-latching defects in the Quick-Release Hook that can cause improper attachment and unexpected detachment, risking patient falls.
The Hillrom Q-Link 13 quick-release hook component used in mobile patient lifts may improperly latch, potentially causing it to detach and result in patient falls.
Baxter is recalling certain Novum IQ syringe pumps due to a design flaw that may cause false syringe detection, resulting in the user interface becoming stuck on the 'Remove Syringe' screen.
Baxter Healthcare is recalling 277 rechargeable batteries used in Hillrom WELCH ALLYN PocketScope handles because they can short circuit and overheat, creating a risk of user burns. The affected lot is 25-043 with expiration August 2027.
Affinity 4 Birthing Beds may have improper signal wire crimps that could prevent lowering the bed or foot section. 164 units have been recalled worldwide.
Baxter is recalling the Novum IQ LVP Infusion System due to potential underinfusion when using standby mode or when powered off with the set loaded. The recall involves 34,524 units in the US and Canada.
Baxter Healthcare is recalling approximately 4,881 units of the Welch Allyn Life2000 Ventilation system worldwide due to a cybersecurity vulnerability discovered through internal testing. No injuries have been reported.
Baxter Healthcare Corporation is recalling approximately 4,174 Welch Allyn Life2000 Compressor units (FDA Class I) due to a cybersecurity vulnerability discovered through internal testing.
Baxter is recalling all 114,202 units of Welch Allyn CONNEX Power Management Stands due to battery-related fires when third-party batteries are used. Only Baxter-approved batteries should be used with these devices.
Baxter Healthcare is recalling 228,412 Welch Allyn Connex Vital Signs Monitors worldwide after customer reports of battery-related fires caused by third-party, non-approved batteries.
Baxter Healthcare is recalling certain Welch Allyn Connex Spot Monitor configurations due to undeclared natural rubber in packaging. Approximately 70,627 units distributed worldwide are affected. Natural rubber presents a latex allergen hazard.
Baxter Healthcare is recalling Welch Allyn Connex Vital Signs Monitors (40,166 units across multiple configurations) due to undeclared natural rubber bands in the packaging. The undeclared allergen poses a risk to individuals with natural rubber latex allergies.
Baxter Healthcare is recalling Welch Allyn reusable blood pressure cuff kits worldwide. Certain configurations contain an undeclared natural rubber band in the packaging.
Baxter Healthcare is recalling certain Welch Allyn Green Series 777 reusable blood pressure cuffs due to undeclared natural rubber in the packaging. People with latex or rubber allergies may experience allergic reactions.
Baxter Healthcare is recalling Welch Allyn DuraShock blood pressure cuff gauge sets worldwide because the packaging contains an undeclared natural rubber band.
Baxter Healthcare Corporation is recalling Welch Allyn Spot Vital Signs 4400 blood pressure cuff devices due to an undeclared natural rubber band in the packaging that could trigger allergic reactions in latex-sensitive individuals.
Baxter Healthcare is recalling Welch Allyn CP150 Electrocardiographs due to reports of battery-related fires. The affected devices used unapproved third-party batteries.
Baxter Healthcare is recalling 8,233 units of Welch Allyn Connex Integrated Wall System reusable blood pressure cuffs worldwide due to undeclared natural rubber bands in product packaging that may cause allergic reactions in sensitive individuals.