Baxter Healthcare Corporation
413 recalls on record · Latest: Aug 19, 2026
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Agency notice ledger
Federal filing book Baxter Healthcare Corporati… HEAVY-BOOK · MULTI-AGENCY
#21 of 14,151 · 413 notices · 0.396% archive
- BOOK 413 notices
- RANK #21 of 14,151
- SHARE 0.396% archive
- AGENCY FDA Devices (376)
- CAT medical devices
- CATS 3 categories
- LATEST Aug 19, 2026
- PHOTO Olympus Corporation
Nearest notice-volume peer: Olympus Corporation of the Americas (1 notice gap)
Baxter Healthcare Corporation accounts for about 0.396% of the 104,423-notice archive on 413 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →
Baxter Healthcare Corporati…'s standing among 14,151 recalling firms
Baxter Healthcare Corporation ranks 21st of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.
Baxter Healthcare Corporati… vs all firms by recall-notice count
Where this firm's archive sits among every tracked recalling manufacturer
413 21st of 14151 higher than 14,130 of 14,151 firms
Firms, banded by distinct federal recall-event inventory
Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-14
Baxter Healthcare Corporati… in the notice-volume neighbourhood
Distinct federal recall events among this firm and nearest nationwide peers
- Biomerieux Inc
Biomerieux Inc
422 notices
- Olympus Corpo…
Olympus Corporation of the Americas
414 notices
- Baxter Health… (this)
Baxter Healthcare Corporation
413 notices
- Fresh Ideatio…
Fresh Ideation Food Group, LLC dba Fresh Creative Cuisine
409 notices
- Philips North…
Philips North America Llc
404 notices
- Bmw
Bmw
400 notices
What this shows Baxter Healthcare Corporation holds about 0.396% of archive notices alongside 413 distinct filings.
How the 413 notices break down
Same federal filing book as the hero total — split by issuing agency, no new counts.
FDA Drug Critical Aug 19, 2026
Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic Container, Frozen Premix, Sterile, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-3508-41.
FDA Devices Critical Aug 19, 2026
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
FDA Devices Critical Jul 8, 2026
Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion Therapy, positive pressure breathing device
FDA Devices Moderate Jul 8, 2026
Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper Back Section H V U component (product code 1909813) on Baxter operating tables
FDA Devices Critical Jul 8, 2026
Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device
FDA Devices Critical Jul 8, 2026
Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device
FDA Devices Critical Jul 8, 2026
Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; Oscillation Lung Expansion Therapy, positive pressure breathing device
FDA Devices Moderate Jun 10, 2026
Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description: Tubing sets with push-on connector on one end (to attach to the Fluid Selector Valve) and a spike or other appropriate connector on the opposite end to attach the source container.
FDA Devices Critical Apr 8, 2026
Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.
FDA Devices Moderate Mar 25, 2026
Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit per package
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 unit per carton Component: N/A
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 Allyn SureTemp Plus 692 (01692-200) thermometers
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-inch (3.0 meters), Product Code 2C8541
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 (2.6 meters), Product Code 2C8571
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 centimeters), Product Code 2C8632
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-inch (3.0 meters), Product Code 2C8537
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), Non-DEHP, Product Code 2R8537
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 Activated Valve, 10 drops/mL, 107-inch (2.7 meters), Product Code 2R8858
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 Activated Valve, Pfoduct code 2C6255
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 centimeters), Product code 2C8610
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 centimeters), Product Code 2H8603
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), Product Code 2C8519
FDA Devices Moderate Oct 22, 2025
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, 0.2 Micron Filter, three CLEARLINK Luer Activated Valves, Backcheck Valve, 10 drops/mL, 102-inch (2.6 meters), Product Code 2C8593
FDA Devices Moderate Oct 22, 2025
CLEARLINK SYSTEM CONTINU-FLO Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves. 10 drops/mL, 96-inch (2.4 meters). Non-DEHP, Product Code 2R8519
FDA Devices Moderate Oct 22, 2025
CLEARLINK SYSTEM EXTENSION SET, Straight-Type Extension Set, Standard Bore, CLEARLINK Luer Activated Valve, Retractable Collar, 7.9-inch (20 centimeters), Product Code 2C8634
FDA Devices Moderate Oct 22, 2025
CLEARLINK SYSTEM Solution Set, Non-Vented, two CLEARLINK Luer Activated Valves, 10 drops/mL, 100-inch (2.5 meters), Product Code 2C8425
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; intravascular administration set
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 Devices Critical Sep 10, 2025
Novum IQ Syringe Pump, Product Code 40700BAX, 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, Made in Ireland, NDC 36000-306-60.
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 Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.
FDA Devices Critical Jul 16, 2025
Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift - Product Code 2040045A; 5) Viking S Mobile Lift - Product Code 2040006; 6) Viking XS Mobile Lift - Product Code 2040007; 7) LikoLight Mobile lift - Product Code 2030001. .
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, P3700E100439, P3700E100441, P3700E100442, P3700E100443, P3700E100444, P3700E100445, P3700E100446, P3700E100448, P3700E100449, P3700E100450, P3700E100453, P3700E100455, P3700E100456, P3700E100457, P3700E100459, P3700E100463, P3700E100468, P3700E100472, P3700E100476, and P3700E100477
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 Critical May 21, 2025
Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.
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; 3) ) Product Code/Part # 67MXXP-B; 4) ) Product Code/Part # 67MXXX-B; 5) ) Product Code/Part # 67NCTP-B; 6) ) Product Code/Part # 67NCTP-B-ECG3A; 7) ) Product Code/Part # 67NCTX-B; 8) ) Product Code/Part # 67NXEX-B; 9) ) Product Code/Part # 67NXTP-B; 10) ) Product Code/Part # 67NXTP-B-ECG3A; 11) ) Product Code/Part # 67NXTX-B; 12)
Baxter Healthcare Corporati… carries an outsized archive share
Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.
Similar recall count
Nearest multi-notice firms by distinct-event totals (413 here — heavy-book).
Similar medical devices volume
Nearest multi-notice firms that share this firm's dominant product category.
Frequently Asked Questions
How many federal recall notices name Baxter Healthcare Corporati…? ▼
PlainRecalls indexes 413 distinct federal recall events naming Baxter Healthcare Corporation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Baxter Healthcare Corporati… sit among other recalling firms? ▼
Baxter Healthcare Corporation ranks #21 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Baxter Healthcare Corporati…'s notices? ▼
FDA Devices accounts for 376 of this firm's 413 indexed notices across 2 issuing agencies.
What product category dominates Baxter Healthcare Corporati…'s filing book? ▼
Filings for Baxter Healthcare Corporation span 3 product categories, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Baxter Healthcare Corporation: 413 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.
Firm-level totals aggregate distinct federal recall events naming Baxter Healthcare Corporation; individual notices remain authoritative on each linked recall page.
Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026