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 10 critical, 40 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 47 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 (48), FDA Drug (2). The date window on this page runs from Jan 22, 2025 to Feb 25, 2026.

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 Moderate Feb 25, 2026

Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product Description: Infusion Pump, one u…

FDA Drug Moderate Feb 4, 2026

Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL 60015 NDC: 0338-0004-02.

FDA Devices Moderate Jan 28, 2026

SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2

FDA Devices Moderate Dec 10, 2025

Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn Two-Piece Blood Pressure Cuff.

FDA Devices Moderate Oct 29, 2025

Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and 01690-400) Thermometers and Welch…

FDA Devices Moderate Oct 22, 2025

CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product code 2C8419

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-i…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 104-inch…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 14-inch (35 centimete…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, Retractable Collar, 10 drops/mL, 120-i…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 120-inch (3.0 meters), No…

FDA Devices Moderate Oct 22, 2025

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

FDA Devices Moderate Oct 22, 2025

CLEARLINK System Paclitaxel Set, Non-Vented with Polyethylene Lined Tubing and CLEARLINK Luer Activated Valve, 0.2 Micron Filter, CLEARLINK Luer Acti…

FDA Devices Moderate Oct 22, 2025

CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, Plus 4-Way Stopcock Extension Set with two CLEARLINK Luer…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 44-inch (111 centime…

FDA Devices Moderate Oct 22, 2025

CLEARLINK System Non_DEHP Extenstion Set, Straight-Type Extension Set, Standard Bore, 1.2 Micron Filter, CLEARLINK Luer Activated Valve, 19-inch (47…

FDA Devices Moderate Oct 22, 2025

CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 112-inch (2.8 meters), Prod…

FDA Devices Moderate Oct 1, 2025

Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8 m), Product Code REF 2C8519; …

FDA Devices Critical Sep 10, 2025

Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump

FDA Devices Critical Sep 10, 2025

Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump

FDA Drug Moderate Sep 3, 2025

Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, …

FDA Devices Moderate Sep 3, 2025

Spectrum IQ Infusion Pump, Product Code 3570009

FDA Devices Critical Aug 20, 2025

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

FDA Devices Critical Jul 23, 2025

Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX

FDA Devices Critical Jul 23, 2025

Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2

FDA Devices Critical Jul 16, 2025

Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product C…

FDA Devices Moderate Jun 18, 2025

2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600

FDA Devices Moderate Jun 18, 2025

Baxter Novum IQ Syringe Pump, product code 40800BAXUS,

FDA Devices Moderate Jun 4, 2025

Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435, P3700E100436, P3700E100437, P3700E100438…

FDA Devices Critical May 28, 2025

Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS

FDA Devices Critical May 21, 2025

Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5) RMS010093CP.

FDA Devices Moderate Apr 23, 2025

Welch Allyn Connex Vital Signs Monitor (CVSM):

FDA Devices Moderate Apr 23, 2025

Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) ) Product Code/Part # 67MXTX-B; …

FDA Devices Moderate Apr 23, 2025

Welch Allyn Welch Allyn Connex Spot Monitor, Product Code/ Part Numbers: 1) 73WT-B; 2) 74CE-B; 3) 74CT-B; 4) 74CX-B; 5) 74ME-B; 6) 74MT-…

FDA Devices Moderate Apr 23, 2025

Welch Allyn CONNEX Accessory Power Management Stand:

FDA Devices Moderate Apr 23, 2025

Welch Allyn DuraShock Aneroid Gauge Sets with a Reusable Blood Pressure Cuff labeled as: 1) WELCH ALLYN DURASHOCK Aneroid Gauge Sets with a Reusab…

FDA Devices Moderate Apr 23, 2025

Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits labeled as: 1. WELCH ALLYN 2-Piece Reusable Blood Pressure Cuff Kits, Product Code/Part Numb…

FDA Devices Moderate Apr 23, 2025

Welch Allyn Spot Vital Signs 4400 Device, Product Code/Part Numbers: 1) 44WT-2; 2) 44WT-3; 3) 44WT-4; 4) 44WT-6; 5) 44WT-B; 6) 44XT-2; …

FDA Devices Moderate Apr 2, 2025

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

FDA Devices Moderate Apr 2, 2025

Baxter Mobile column TruSystem 7500 U, Product Code 1730720

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500, Product Code 4091000

FDA Devices Moderate Apr 2, 2025

Baxter Stationary column TruSystem 7500, Product Code 1717020

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (MC), Product Code 1773204

FDA Devices Moderate Apr 2, 2025

Baxter TruSystem 7500 Hybrid (SC), Product Code 1854086

FDA Devices Moderate Apr 2, 2025

Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS

FDA Devices Critical Mar 12, 2025

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

FDA Devices Moderate Jan 29, 2025

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

FDA Devices Moderate Jan 29, 2025

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

FDA Devices Moderate Jan 29, 2025

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

FDA Devices Critical Jan 22, 2025

Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002

Nearby Manufacturers

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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