Baxter Healthcare Corporation recalls

125 recalls on record · latest: February 18, 2026

Official U.S. recall history for Baxter Healthcare Corporation, compiled from official government records.

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Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory…

February 18, 2026 · Medical device recalls High risk Urgent Medical Device Correction for the Volara system single-patient use circu…

Baxter Healthcare Corporation recalls Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software…

February 18, 2026 · Medical device recalls Moderate risk Display screen may unintentionally flicker due to a software issue. Exposure to…

Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Descrip…

January 13, 2026 · Medical device recalls Moderate risk Pumps were released without full testing being performed, including occlusion a…

Baxter Healthcare Corporation recalls Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL…

December 22, 2025 · Drug & medication recalls Moderate risk Presence of particulate matter: plastic particles from the bottle rim were obse…

Baxter Healthcare Corporation recalls SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2

November 28, 2025 · Medical device recalls Moderate risk Certain pumps have potentially been released from service with defective grease…

Baxter Healthcare Corporation recalls Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn T…

October 28, 2025 · Medical device recalls Moderate risk Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure c…

Baxter Healthcare Corporation recalls Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 016…

September 17, 2025 · Medical device recalls Moderate risk Affected oral/axillary probes were inadvertently programmed with the rectal pro…

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Pro…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 m…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activated Valves, Backch…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/m…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Filter, CLEARLINK Luer…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock Extensi…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micr…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SET, 96" (2,4 m), Product Code: 2H8519

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retracta…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activated Valves, Backchec…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retracta…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product cod…

August 29, 2025 · Medical device recalls Moderate risk IV sets may leak.

Baxter Healthcare Corporation recalls Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corp…

August 20, 2025 · Drug & medication recalls Moderate risk Discoloration

Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8…

August 8, 2025 · Medical device recalls Moderate risk Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for on…

Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump

August 4, 2025 · Medical device recalls High risk Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction fo…

Baxter Healthcare Corporation recalls Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

August 4, 2025 · Medical device recalls High risk Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction fo…

Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

August 4, 2025 · Medical device recalls High risk Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction fo…

Baxter Healthcare Corporation recalls Spectrum IQ Infusion Pump, Product Code 3570009

July 14, 2025 · Medical device recalls Moderate risk Baxter has identified that certain pumps have potentially been released with th…

Baxter Healthcare Corporation recalls Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS

July 14, 2025 · Medical device recalls High risk Baxter is issuing an Urgent Medical Device Correction for the Novum IQ large vo…

Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2

June 20, 2025 · Medical device recalls High risk Certain Spectrum infusion pumps may have an incorrect version of software.

Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX

June 20, 2025 · Medical device recalls High risk Certain Spectrum infusion pumps may have an incorrect version of software.

Baxter Healthcare Corporation recalls Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile l…

May 30, 2025 · Medical device recalls High risk The Q-link 13 could allow for an improper attachment (false latching) of the Qu…

Baxter Healthcare Corporation recalls Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale…

May 30, 2025 · Medical device recalls High risk The Q-link 13 could allow for an improper attachment (false latching) of the Qu…

Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, product code 40800BAXUS,

May 12, 2025 · Medical device recalls Moderate risk Baxter has identified a design issue which may cause the pump to detect the pre…

Baxter Healthcare Corporation recalls 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600

May 9, 2025 · Medical device recalls Moderate risk The replacement rechargeable batteries inserted into the Welch Allyn PocketScop…

Baxter Healthcare Corporation recalls Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E1004…

May 6, 2025 · Medical device recalls Moderate risk There is a potential for improper crimps on the signal wires of the actuators w…

Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

April 24, 2025 · Medical device recalls High risk There is a potential for the Novum IQ LVP due to the potential for underinfusio…

Baxter Healthcare Corporation recalls Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5)…

April 7, 2025 · Medical device recalls High risk A cybersecurity vulnerability was discovered through internal testing.

Baxter Healthcare Corporation recalls Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010…

April 7, 2025 · Medical device recalls High risk A cybersecurity vulnerability was discovered through internal testing.

Welch Allyn CP150 Electrocardiograph recalled over fire hazard

March 24, 2025 · Medical device recalls Moderate risk There were customer reports of devices which experienced battery-related fires.…

Welch Allyn CONNEX Accessory Power Management Stand recalled over fire hazard

March 24, 2025 · Medical device recalls Moderate risk There were customer reports of devices which experienced battery-related fires.…

Welch Allyn Connex Vital Signs Monitor recalled over fire hazard

March 24, 2025 · Medical device recalls Moderate risk There were customer reports of devices which experienced battery-related fires.…

Welch Allyn Connex Integrated Wall System recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Welch Allyn Green Series 777 Wall System recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Welch Allyn Spot Vital Signs 4400 Device recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Welch Allyn Reusable Blood Pressure Cuff Kits labeled as: 1 recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Baxter Healthcare product recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Welch Allyn Welch Allyn Connex Spot Monitor recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Welch Allyn Connex Vital Signs Monitor recalled over undeclared natural

March 21, 2025 · Medical device recalls Moderate risk Undeclared natural rubber band within the packaging of certain configurations o…

Baxter Healthcare Corporation recalls Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

March 3, 2025 · Medical device recalls Moderate risk Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for th…

Baxter Healthcare Corporation recalls Baxter Mobile column TruSystem 7500, Product Code 1717023

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Floor mounting column TS 7500 U, Product Code 1730732

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Floor mounting column TruSystem 7500, Product Code 1717021

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (SC), Product Code 1854088

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (FC), Product Code 1854085

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with immobi…

February 25, 2025 · Medical device recalls Moderate risk The air bladders inside the mattress may move out of position when the head of…

Baxter Healthcare Corporation recalls Baxter Operating table column TS7500 MOBIUS, Product Code 1704695

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid MR IMRIS, Product Code 2067886

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Stationary column TruSystem 7500 U, Product Code 1730731

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Stationary column TruSystem 7500, Product Code 1717020

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500, Product Code 4091000

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Mobile column TruSystem 7500 U, Product Code 1730720

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087

February 25, 2025 · Medical device recalls Moderate risk There is a software issue which causes the upper back section to not be operabl…

Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009

February 5, 2025 · Medical device recalls High risk There is the potential for missing motor mounting screws, which may have occurr…

Baxter Healthcare Corporation recalls Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX

February 5, 2025 · Medical device recalls High risk There is the potential for missing motor mounting screws, which may have occurr…

Baxter Healthcare Corporation recalls Baxter Clearlink System Solution Set with Duo-Vent Spike, REF 2R8538

December 20, 2024 · Medical device recalls Moderate risk Specific lots of Solution Sets with Duo-Vent Spike have the potential for inver…

Baxter Healthcare Corporation recalls Baxter Solution Set with Duo-Vent Spike, REF 2R8404

December 20, 2024 · Medical device recalls Moderate risk Specific lots of Solution Sets with Duo-Vent Spike have the potential for inver…

Baxter Healthcare Corporation recalls Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519

December 20, 2024 · Medical device recalls Moderate risk Specific lots of Solution Sets with Duo-Vent Spike have the potential for inver…

Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A

December 20, 2024 · Medical device recalls High risk There is an issue with the ventilator battery charger that could lead to an aud…

Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002AP

December 20, 2024 · Medical device recalls High risk There is an issue with the ventilator battery charger that could lead to an aud…

Baxter Healthcare Corporation recalls Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP

December 20, 2024 · Medical device recalls High risk There is an issue with the ventilator battery charger that could lead to an aud…

Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002

December 20, 2024 · Medical device recalls High risk There is an issue with the ventilator battery charger that could lead to an aud…

Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX

November 19, 2024 · Medical device recalls Moderate risk Devices were identified as released after repair without full testing being per…

Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2

November 19, 2024 · Medical device recalls Moderate risk Devices were identified as released after repair without full testing being per…

Baxter Healthcare Corporation recalls Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL), 5mL Single-Dose Pre-filled Syringe, Rx only, Manufactured by: Baxter P…

October 30, 2024 · Drug & medication recalls Moderate risk Labeling: Missing Label

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialys…

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialy…

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

October 23, 2024 · Medical device recalls Moderate risk There has been an increase in the number of complaints related to the separatio…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis

October 21, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…

Baxter Healthcare Corporation recalls Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is…

October 16, 2024 · Medical device recalls High risk Baxter is aware of several recalls by other manufacturers related to the potent…