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Baxter Healthcare Corporation recall records

273 reported ongoing

306 records in this archive. Latest source date Aug 17, 2026.

FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

Records and reported status

Oct 21, 2024FDA device enforcement

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

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 hemodialy...

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 21, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: Worldwide Distribution (US Nationwide distribution)

Official source

Oct 16, 2024FDA device enforcement

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

Class IReported ongoing

Distribution: US Nationwide distribution and worldwide

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn HScribe Holter System; ambulatory monitoring

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 mismat...

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn Q-Stress Cardiac Stress Testing System; cardiac stress test

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System; Electrocardiograph

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn Diagnostic Cardiology Suite (formerly Connex Cardio); Diagnostic spirometer

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 11, 2024FDA device enforcement

Hillrom Welch Allyn XScribe Cardiac Stress Testing System; Programmable Diagnostic Computer

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Oct 2, 2024FDA device enforcement

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

The door on the Spectrum IQ Infusion pump may not be able to fully close.

Class IIReported ongoing

Distribution: GA, ID

Official source

Sep 19, 2024FDA device enforcement

Baxter Operating table TruSystem 7000 U (MB), Product codes: a) REF 1604786; b) REF 1604788; c) REF 1723633

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Sep 19, 2024FDA device enforcement

Baxter Operating Table TruSystem 7000, Product code REF 1841046

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Sep 19, 2024FDA device enforcement

Baxter Operating Table TruSystem 7000 (MBW), Product code REF 1841048

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Sep 19, 2024FDA device enforcement

Baxter Operating Table TruSystem 7000 (dV), Product code REF 1841049

The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

Class IIReported ongoing

Distribution: Worldwide distribution.

Official source

Reasons in these listed records

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.
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 ...
The door on the Spectrum IQ Infusion pump may not be able to fully close.
The firm received customer reports stating that the batteries and their connectors experienced electrical short-circuits and/or emitted smoke.

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This archive contains 306 records, including 273 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product.

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Use monthly archives or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page.

Records and reported status

Reasons in these listed records

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