PlainRecalls

Baxter Healthcare Corporation

286 recalls on record · Latest: Feb 25, 2026

Baxter Healthcare Corporation Recall Insight

Baxter Healthcare Corporation appears on 286 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.341% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Feb 25, 2026, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 13 critical, 37 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 3 distinct product categories, with issuing agencies dominated by FDA Devices (47), FDA Drug (3). The date window on this page runs from Apr 10, 2024 to Jan 22, 2025.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Critical Jan 22, 2025

Breathe Technologies, Inc., Life2000 Ventilation System, REF BT-20-0002AP

FDA Devices Moderate Jan 8, 2025

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

FDA Devices Moderate Jan 8, 2025

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

FDA Devices Moderate Dec 4, 2024

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

FDA Devices Moderate Dec 4, 2024

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

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set (short) with Titanium Spike, Part Number T5C4326K; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

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

FDA Devices Moderate Dec 4, 2024

Baxter MiniCap Extended Life PD Transfer Set (long) with Titanium Spike, Part Number T5C4325K; use in Peritoneal Dialysis

FDA Devices Moderate Dec 4, 2024

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

FDA Devices Critical Nov 27, 2024

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

FDA Devices Critical Nov 27, 2024

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

FDA Devices Critical Nov 27, 2024

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

FDA Devices Critical Nov 27, 2024

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

FDA Devices Critical Nov 27, 2024

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

FDA Devices Moderate Nov 20, 2024

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

FDA Drug Moderate Nov 13, 2024

Regadenoson Injection, 0.4 mg/5 mL (0.08 mg/mL), 5mL Single-Dose Pre-filled Syringe, Rx only, Manufactured by: Baxter Pharmaceutical Solutions, LLC, …

FDA Devices Moderate Nov 13, 2024

Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph

FDA Devices Moderate Nov 13, 2024

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

FDA Devices Moderate Nov 13, 2024

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

FDA Devices Moderate Nov 6, 2024

a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed, Product codes: P7900B000001, P7900B100010, P7900B100024, P7900B100208, P7900B100273, P79…

FDA Devices Moderate Oct 30, 2024

Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083

FDA Devices Moderate Oct 30, 2024

Baxter Operating Table TruSystem 7000 U14 (MBW), Product code REF 2065385

FDA Devices Moderate Oct 30, 2024

Baxter Operating Table TruSystem 7000 (MBW) V, Product code REF 1841082

FDA Devices Critical Oct 30, 2024

Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A, 3) BT-20-0002AP, 4) BT-20-0007…

FDA Devices Moderate Oct 30, 2024

Baxter Operating Table TruSystem 7000 V, Product code REF 1841050

FDA Devices Moderate Oct 30, 2024

Baxter Operating Table TruSystem 7000, Product code REF 1841046

FDA Devices Moderate Oct 30, 2024

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

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, High Volume Inlet, REF H938174, for use in a pharmaceutical compounding device

FDA Devices Critical Sep 25, 2024

Baxter EXACTAMIX Inlet, Vented, Micro-Volume Inlet, REF H938175, for use in a pharmaceutical compounding device

FDA Drug Critical Sep 11, 2024

Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile Single Dose Container, Rx Only, Ba…

FDA Devices Moderate Aug 28, 2024

Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8 infusion pump) and 3570009 (S…

FDA Devices Moderate Aug 28, 2024

Baxter Spectrum Wireless Battery Modules A/B/G/N, product code 35223, used with either of the following: 35700BAX2 (Spectrum V8 infusion pump) or 35…

FDA Devices Moderate Aug 14, 2024

Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2

FDA Devices Moderate Aug 14, 2024

Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300

FDA Devices Critical Jul 24, 2024

Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit kit for Volara. Intermittent positive pressure …

FDA Drug Moderate Jul 17, 2024

Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration Only, 6000 mL per bag, Rx Only, B…

FDA Devices Moderate Jul 17, 2024

Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools that clinicians us…

FDA Devices Moderate Jul 17, 2024

Braun Thermoscan¿ PRO 6000 Ear Thermometer

FDA Devices Moderate Jul 17, 2024

Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)

FDA Devices Moderate Jul 17, 2024

iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Sur…

FDA Devices Moderate Jul 17, 2024

VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgica…

FDA Devices Critical Jul 3, 2024

Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and B…

FDA Devices Moderate Jun 26, 2024

Centrella Max - The Centrella Smart+ Bed is intended for use in healthcare environments as a patient support system to prevent and/or treat pressure …

FDA Devices Moderate May 1, 2024

Baxter Seprafilm Adhesion Barrier 1 Half Sheet, 5-PK, REF 664103, for use in abdominal and pelvic surgery

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

FDA Devices Moderate Apr 24, 2024

Surgical Tools and Cardiovascular Specialty marketing brochures, Reference numbers: US-AS18-210002 Surgical Tools Brochure 2021, US-AS18-210004 Surg…

FDA Devices Moderate Apr 17, 2024

Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models: a) PROBP 3400, SUREBP, BLUETOOTH, MOBILE…

FDA Devices Moderate Apr 10, 2024

Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or treatment of pressure in…

Nearby Manufacturers

Other firms with recall activity tracked in the PlainRecalls index.

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds