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Baxter Healthcare Recalls
556 recalls on record · June 20, 2012 to August 19, 2026 · Drugs, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Floor mounting column TS 7500 U, Product Code 1730732
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Stationary column TruSystem 7500 U, Product Code 1730731
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Mobile column TruSystem 7500 U, Product Code 1730720
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Mobile column TruSystem 7500, Product Code 1717023
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Floor mounting column TruSystem 7500, Product Code 1717021
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Stationary column TruSystem 7500, Product Code 1717020
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
April 2, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating table column TS7500 MOBIUS, Product Code 1704695
Hazard: There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
March 12, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Hazard: There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
March 12, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Hazard: There is the potential for missing motor mounting screws, which may have occurred during the servicing process.
January 29, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519
Hazard: Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
January 29, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538
Hazard: Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
January 29, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Hazard: Specific lots of Solution Sets with Duo-Vent Spike have the potential for inverted side clamps causing the tubing to be unusable.
January 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP
Hazard: There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
January 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002AP
Hazard: There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
January 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A
Hazard: There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
January 22, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
Hazard: There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.
January 8, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Hazard: Devices were identified as released after repair without full testing being performed, which includes flow testing.
January 8, 2025Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Hazard: Devices were identified as released after repair without full testing being performed, which includes flow testing.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialy
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialys
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
Hazard: There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.