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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.
December 4, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; 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 5C4483; 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 5C4482S; 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 5C4482EJ; 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 5C4482; 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.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp EX Short, Part Number T5C4484; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number T5C4482; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4484; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4483; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482E; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number R5C4482; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4483; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482S; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 27, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 20, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Hazard: The door on the Spectrum IQ Infusion pump may not be able to fully close.
November 20, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is
Hazard: Baxter is aware of several recalls by other manufacturers related to the potential risk of exposure to non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs) and NDL polychlorinated biphenyls (PCBs) when using certain peritoneal dialysis and hemodialysis devices.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn XScribe Cardiac Stress Testing System; Programmable Diagnostic Computer
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn Diagnostic Cardiology Suite (formerly Connex Cardio); Diagnostic spirometer
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System; Electrocardiograph
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Hillrom Welch Allyn HScribe Holter System; ambulatory monitoring
Hazard: There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS)) relies solely on the UID to accept exams, this could lead to a mismatch of the patients identification with their physiological data.
November 13, 2024DrugsFDA
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 Ph
Hazard: Labeling: Missing Label
November 6, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed, Product codes: P7900B000001, P7900B100010, P7900B100024, P7
Hazard: The beds have a potential for an interface issue with the Rauland Responder 5 Nurse Call System where the bed exit system will alert at the bed, but may fail to send a remote alert through the nurse call system.
October 30, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 U14 (MBW) V, Product code REF 2065386
Hazard: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
October 30, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 U14 (MBW), Product code REF 2065385
Hazard: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
October 30, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
Hazard: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
October 30, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 (MBW) V, Product code REF 1841082
Hazard: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.
October 30, 2024Medical DevicesFDA
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 V, Product code REF 1841050
Hazard: The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.