Baxter Healthcare Corporation recalls
Every recall we track for Baxter Healthcare Corporation — 431 in all, from 2015–2026 — plus the complaints and injury reports the public filed about them. 25 are rated “stop using now”.
Recalls per year, by danger level
Recalls from Baxter Healthcare Corporation peaked in 2024 (87); 428 since 2017. 5% rated “stop using now”.
All FDA recall records for Baxter Healthcare Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 1 | 3 | 5 | 3 | 12 |
| 2018 | 1 | 15 | 15 | 6 | 37 |
| 2019 | 3 | 10 | 4 | 1 | 18 |
| 2020 | 1 | 6 | 25 | 2 | 34 |
| 2021 | 0 | 6 | 11 | 1 | 18 |
| 2022 | 2 | 21 | 44 | 7 | 74 |
| 2023 | 3 | 8 | 32 | 3 | 46 |
| 2024 | 4 | 38 | 36 | 9 | 87 |
| 2025 | 5 | 30 | 25 | 5 | 65 |
| 2026 (to date) | 3 | 8 | 9 | 17 | 37 |
Baxter Healthcare Corporation recalls before 2017
Recalls on record by year.
Most common reasons for Baxter Healthcare Corporation recalls
What to do if you have a recalled Baxter Healthcare Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Baxter Healthcare Corporation recalls
60 shown- Use cautionMedical device
Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product
Baxter Healthcare recalls Likorall Overhead Lifts with potential motor shaft breakage causing uncontrolled drop. Affected models include LIKORALL 200, 242, 243, and 250 series. Stop using immediately if you own these lifts.
Baxter HealthcareSep 14, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls PRO+ 40" MRS SURFACE, mattress with Advanced Microclimate Technology (AMT) uses a non-powered system of intake and
Baxter Healthcare recalls PRO+ 40" MRS SURFACE mattresses with AMT technology due to UDI label errors that may cause incorrect bed frame selection. Affected units have specific serial numbers and model numbers.
Baxter HealthcareAug 18, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA,
Baxter recalls 2000mL dextrose injection bags with stainless steel particles. Stop using immediately due to potential serious injury from particulate matter in IV solutions.
Baxter HealthcareAug 17, 2026 - Stop using nowDrug
Baxter Healthcare Corporation recalls 0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare
Baxter recalls 500mL saline injections in VIAFLEX plastic containers due to fiberglass particulates. Stop using if you have these containers with specific lot numbers.
Baxter HealthcareAug 17, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
Baxter recalls Novum IQ Syringe Pump model 40800BAXUSL due to software issue that may cause infusion errors when syringes are replaced during multi-syringe infusions. Affected units have specific serial numbers.
BaxterAug 11, 2026 - UnratedDrug
Baxter Healthcare Corporation recalls Pantoprazole Sodium in 0.9% Sodium Chloride Injection, 80 mg/100 mL (0.8 mg/mL) Single-Dose Infusion Bag in 100 mL
Baxter recalls Pantoprazole Sodium 80mg/100mL injection due to CGMP deviations. Affected lots may have quality issues affecting safety. Contact for details.
BaxterAug 6, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Brand Name: VOLARA System Product Name: VOLARA, HC, NA A Model/Catalog Number: M08594A Software Version: N/A Product
Baxter recalls VOLARA System (model M08594A) due to potential contamination affecting nebulizer flow rate accuracy. Affected units were tested and confirmed safe after return.
BaxterAug 3, 2026 - Use cautionDrug
Baxter Healthcare Corporation recalls Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL) Single-Dose Infusion Bag in 100mL GALAXY Plastic
Baxter Healthcare recalls Cefazolin injection bags with particulate matter. Affected units contain lot # LD175708, expiring Feb 2027. Consumers should contact Baxter for details.
BaxterJul 24, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Baxter recalls Duo-Vent Solution Sets with air bubbles in drip chamber when pressure cuff is used or tubing flushed fully open. Affected units have specific product codes and expiration dates.
BaxterJun 30, 2026 - Use cautionMedical device
Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung
Hillrom recalls Volara System circuit kits with potential air leaks causing oxygen drops. Affected units have model REF M08473 and were sold starting April 28, 2025. Stop using if leaks occur.
HillromMay 21, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number: H938175 Product Description:
Baxter Healthcare recalls Exacta Mix Vented Micro-Volume Inlet model H938175 with incorrect 0.8-micron filters that may cause incomplete or slower transfers of ingredients, leading to clinical effects like electrolyte imbalance.
Exacta MixApr 22, 2026 - Use cautionMedical device
Baxter Healthcare Corporation recalls Adapter for Head Positioning, Model/Catalog Number: 1739994, when used in conjunction with the side rails of the Upper
Baxter recalls head positioning adapter model 1739994 for possible loosening when used with operating table side rails, risking unintended movement during patient positioning.
BaxterApr 21, 2026 - Use cautionMedical device
Baxter Healthcare Corporation recalls Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software
Welch Allyn recalls VS100 Spot Vision Screener software version 3.2.0.1 due to potential flickering that could trigger photosensitive seizures in susceptible individuals. Affected units sold with specific model and software version.
Welch AllynFeb 18, 2026 - Stop using nowMedical device
Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory
Baxter recalls Blue Ventil: single-patient use circuit for oxygen desaturation or lung injury risk in home care. Affected units have Product Code M07937. Contact for remedy.
Baxter HealthcareFeb 18, 2026 - Lower riskMedical device
Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 Software Version: N/A Product
Baxter Healthcare recalls Spectrum IQ Infusion Pump model 3570009 due to untested occlusion alarms, which may lead to inaccurate medication dosing. Affected units have specific serial numbers and lot codes.
Spectrum IQJan 13, 2026 - Lower riskDrug
Baxter Healthcare Corporation recalls Sterile Water for Irrigation, 250 mL, Single-Dose Plastic Bottle, Rx Only, Baxter Healthcare Corporation Deerfield, IL
Baxter Healthcare recalls 250mL single-dose sterile water bottles due to plastic particles floating into the solution. This may cause infection or injury during medical use.
Baxter HealthcareDec 22, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls SIGMA Spectrum Infusion Pump, Model/Catalog Number: 35700BAX2
Baxter recalls SIGMA Spectrum Infusion Pump Model 35700BAX2 with defective grease that may cause pump failure. Affected units have serial numbers listed in the recall notice.
BaxterNov 28, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Welch Allyn INF BAG, Thigh 1-Tube, Model/Catalog Number: REF 5089-18; Product replacement bladder for the Welch Allyn
Welch Allyn recalls replacement bladders for blood pressure cuffs that may be the wrong size, risking inaccurate readings. Affected units include specific model and lot numbers.
Welch AllynOct 28, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Oral Probe (Product code 02893-000), accessory used with Welch Allyn SureTemp Plus 690 (Product codes 01690-200 and
Baxter Healthcare Corporation product codes and serial numbers for various medical devices and equipment.
Baxter Healthcare CorporationSep 17, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls CLEARLINK System Solution Set, DUO-VENT, CLEARLINK Luer Activated Valve, 10 drops/mL, 92-inch (2.3 meters), Product
Baxter Healthcare recalls CLEARLINK System Solution Sets with potential leakage. Affected units have specific product codes and lot numbers. Stop using if leaks occur to prevent IV fluid loss.
Baxter HealthcareAug 29, 2025 - Lower riskDrug
Baxter Healthcare Corporation recalls Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare
Baxter Healthcare recalls acetaminophen injection with discoloration risk. Check product details to determine if affected. Stop using if discoloration observed.
Baxter HealthcareAug 20, 2025 - Stop using nowMedical device
Baxter Healthcare Corporation recalls Baster Continu-Flo Solution Set, Non-Vented, 2 Clearlink Luer Activated Valves, Backcheck Valve. 10 drops/mL. 112" (2.8
Baxter Healthcare recalls Continu-Flo solution sets with tubing separation risk. Affected units have specific lot numbers and expiration dates. Stop using immediately to prevent medical complications.
Baxter HealthcareAug 8, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump
Baxter Healthcare recalls Novum IQ Syringe Pumps with software anomalies that may cause blank run screens or false motor errors. Affected units include Product Code 40800BAXUS with specific serial numbers.
Baxter HealthcareAug 4, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Spectrum IQ Infusion Pump, Product Code 3570009
Baxter recalls Spectrum IQ Infusion Pumps with Product Code 3570009 due to potential grease breakdown causing premature wear and ineffective therapy. Affected units have specific serial numbers.
BaxterJul 14, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter Novum IQ Large Volume Pump, Product Code REF 40700BAXUS
Baxter recalls Novum IQ Large Volume Pumps due to potential underinfusion when changing flow rates. This may cause incorrect medication delivery. Affected units have specific product codes and serial numbers.
BaxterJul 14, 2025 - UnratedMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
Baxter recalls Spectrum Infusion Pump V6 Model 35700BAX with incorrect software version. Affected units may have safety risks; contact Baxter for details.
BaxterJun 20, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale
Baxter Healthcare recalls Hillrom LikoScale component (Product Code 3156232) used with specific adapter kits for patient lifts due to risk of patient falls from improper attachment of Quick-Release Hook.
HillromMay 30, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, product code 40800BAXUS,
Baxter recalls Novum IQ syringe pumps with design flaw causing 'Remove Syringe' screen to stay on after infusion. Only affects models made or repaired after July 4, 2023. No remedy specified in recall notice.
BaxterMay 12, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls 2.5 V replacement rechargeable batteries for Hillrom WELCH ALLYN PocketScope handles, Product Code 72600
Baxter Healthcare recalls 2.5V rechargeable batteries for Welch Allyn PocketScope handles that may cause short circuits and burns. Product code 72600, lot 25-043, expires August 2027.
Baxter HealthcareMay 9, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Affinity 4 Birthing Bed, Product Codes P3700E100429, P3700E100432, P3700E100433, P3700E100434, P3700E100435,
Baxter Healthcare recalls Affinity 4 Birthing Beds with specific product codes due to potential signal wire crimps causing loss of bed lowering function.
Baxter HealthcareMay 6, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter Novum IQ LVP INFUSION SYSTEM, REF 40700BAXUS
Baxter recalls Novum IQ LVP Infusion System (REF 40700BAXUS) due to potential underinfusion if standby mode is used or device is powered off with set loaded. All units affected.
BaxterApr 24, 2025 - UnratedMedical device
Baxter Healthcare Corporation recalls Welch Allyn Life2000 Compressor, Product Codes: 1) BT-80-0004; 2) BT-80-0004A; 3) BT-80-0008; 4) BT-80-0008A; 5)
Baxter Healthcare recalls Welch Allyn Life2000 Compressors with specific product codes due to a cybersecurity vulnerability found during internal testing.
Welch AllynApr 7, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor (CVSM):
Baxter Healthcare recalls Welch Allyn Connex Vital Signs Monitors with third-party batteries that can cause fires. All units with specific serial numbers and product codes are affected.
Welch AllynMar 24, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitor, Product Code/Part Numbers: 1) ) Product Code/Part # 67MXTP-B-ECG3A; 2) )
Baxter Healthcare Corporation recalls Welch Allyn Connex Vital Signs Monitors with certain blood pressure cuff models due to undeclared natural rubber bands in packaging that could cause injury.
Welch AllynMar 21, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter NovumIQ Syringe INFUSION SYSTEM , REF 40800BAXUS
Baxter recalls NovumIQ syringe pumps with serial numbers starting 02A220600103 due to an incorrectly installed gasket that could allow fluid to enter the pump during cleaning or IV spills.
BaxterMar 3, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Progressa Bed Surfaces, intended to be used to treat or prevent pulmonary or other complications associated with
Baxter Healthcare recalls Progressa Bed Surfaces with product codes P7520A19 to P7520A4S. Air bladders may move out of position when the head of the bed is elevated, causing a dip in the mattress. Consumers should check if their unit has the listed serial numbers or product codes.
Baxter HealthcareFeb 25, 2025 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter TruSystem 7500 Hybrid Plus (FC), Product Code 1854087
Baxter recalls TruSystem 7500 Hybrid Plus (FC) with software issue where emergency mode makes upper back section unadjustable. Affected units have product code 1854087 and serial numbers up to 11/14/2024.
BaxterFeb 25, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Baxter recalls Sigma Spectrum Infusion System (V6 Platform) with Product Code 35700BAX due to potential missing motor mounting screws during servicing. Affected units have specific serial numbers.
BaxterFeb 5, 2025 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519
Baxter recalls specific lots of Continu-Flo Solution Sets with Duo-Vent Spike due to inverted side clamps that can make tubing unusable. Affected units have lot numbers DR24B21017 (expiring 02/28/2026).
BaxterDec 20, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Welch Allyn, Inc., Life 2000 Ventilation System, REF BT-20-0002
Welch Allyn Life 2000 Ventilation System with specific serial numbers recalled due to battery charger alarm malfunction that can disable ventilator operation.
Welch AllynDec 20, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Baxter recalls SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) due to potential flow testing issues after repair. Affected units may have safety risks.
BaxterNov 19, 2024 - Use cautionDrug
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
Baxter Healthcare recalls 60,594 units of Regadenoson Injection syringes because the label is missing. Check lot numbers and expiration dates.
BaxterOct 30, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482EJ; use in Peritoneal Dialysis
Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (part 5C448: 5C4482EJ) for potential female connector separation during peritoneal dialysis use.
BaxterOct 23, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, Part Number 5C4482; use in Peritoneal Dialysis
Baxter recalls MiniCap Extended Life PD Transfer Sets with Twist Clamp (Part 5C4482) used in peritoneal dialysis due to potential PCB exposure risks. Affected units include all lots manufactured after H19I2:6088.
BaxterOct 21, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter AK 98 Dialysis Machine, Hemodialysis Delivery System, Product Code 955607. As of February 2025, the firm name is
Baxter recalls AK 98 Dialysis Machines with specific serial numbers due to potential exposure to PCBs during use. Affected units have runtime under 500 hours.
BaxterOct 16, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System; Electrocardiograph
Baxter Healthcare Corporation recalls Hillrom Welch Allyn Vision Express Holter Analysis System software versions V6.1.0 to V6.4.1 due to potential duplicate patient ID assignments in medical records, which could cause misidentification of patient data.
Hillrom Welch AllynOct 11, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Baxter recalls Spectrum IQ Infusion System with Dose IQ Safety Software (Product Code 3570009) due to door not closing fully, which could lead to infusion errors.
BaxterOct 2, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter Operating Table TruSystem 7000 (dV) V, Product code REF 1841083
Baxter Healthcare recalls TruSystem 7000 operating tables with battery short circuits and smoke emission risks. Affected units may cause fire or injury. Contact for return or repair.
Baxter HealthcareSep 19, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls a. Hillrom Centrella Smart+ Medical-Surgical Hospital Bed, Product codes: P7900B000001, P7900B100010, P7900B100024,
Hillrom recalls Centrella Smart+ hospital beds with specific product codes due to potential interface failure with nurse call systems, risking missed alerts. Affected units may need verification.
HillromSep 18, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Welch Allyn Life2000 Ventilation System, REF MS-01-0118, within exterior carton codes: 1) BT-20-0002, 2) BT-20-0002A,
Baxter Healthcare recalls Welch Allyn Life2000 Ventilation Systems with specific carton codes and software versions due to potential failure to trigger low gas pressure alarms if gas source isn't connected before use.
Welch AllynSep 12, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Baxter EXACTAMIX Inlet, Vented, Syringe Inlet, REF H938176, for use in a pharmaceutical compounding device
Baxter recalls EXACTAMIX Inlet syringes (H938176) due to particulate matter in the sterile fluid path. Affected units sold with ExactaMix and ExactaMix Pro compounders. Contact Baxter for details.
BaxterAug 20, 2024 - Use cautionDrug
Baxter Healthcare Corporation recalls Heparin (Heparin Sodium in 0.9% Sodium Chloride Injection), 2,000 units per 1,000 mL (2 units/mL), 1000 mL Sterile
Baxter recalls 1000mL heparin injections with microbial contamination risk. Out of limit endotoxin test results found in specific lots. Stop using if you have this product.
BaxterAug 1, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Spectrum Wireless Battery Modules A/B/G/N, product code 36010, used with either of the following 35700BAX2 (Spectrum V8
Baxter recalls Spectrum Wireless Battery Modules A/B/G/N (product code 36010) used with Spectrum V8 or IQ infusion pumps. These modules may fail to auto-document infusion status to hospital EMR systems, potentially causing data gaps in patient care.
Baxter HealthcareJul 17, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Baxter PST 500 U, Precision Surgical Table, Part number (product code) 4080300
Baxter recalls PST 500 U Precision Surgical Tables with loose spring pins that could cause unexpected tabletop movement during surgery, risking patient safety. Affected units have specific serial numbers.
BaxterJun 28, 2024 - Use cautionDrug
Baxter Healthcare Corporation recalls Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose, For Intraperitoneal Administration
Baxter recalls Dianeal Low Calcium (2.5 mEq/L) peritoneal dialysis solution with 2.5% dextrose due to potential leaks from connector assembly. This could risk infection during dialysis. Check NDC 0941-0457-01 and lot R24B25FA.
Baxter HealthcareJun 17, 2024 - UnratedMedical device
Baxter Healthcare Corporation recalls Baxter SIGMA Spectrum Infusion Pump, Product Code: 35700BAX2
Baxter recalls SIGMA Spectrum Infusion Pumps with product code 3570: improper testing before release may cause safety issues. Affected units have serial number 2158913.
BaxterJun 14, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Braun Thermoscan¿ PRO 6000 Ear Thermometer
Braun recalls Thermoscan PRO 6000 ear thermometers with outdated instructions that could lead to incorrect readings. Affected units have specific product codes and serial numbers.
BraunJun 13, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical
Baxter recalls Trulight 5000/3000 surgical lights with specific model numbers due to reported thermal skin injuries. Affected units include Duo and Trio/Quad models with listed serial numbers.
BaxterJun 4, 2024 - Lower riskMedical device
Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one
Baxter Healthcare recalls Welch Allyn CP150 Electrocardiograph with Spirometry Option (CP150A-1ENB) due to missing EMI absorber during manufacturing, potentially causing device malfunction.
Welch AllynJun 3, 2024 - Use cautionMedical device
Baxter Healthcare Corporation recalls Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit kit for Volara.
Baxter Healthcare recalls Volara System Single Patient Use Circuit kits due to risk of handset plug disconnecting from ventilator adapter, potentially causing improper gas flow. Affected units have specific product codes and lot numbers listed.
Baxter HealthcareMay 30, 2024
Baxter Healthcare Corporation recall questions
How many recalls has Baxter Healthcare Corporation had?
431 recalls from Baxter Healthcare Corporation are on record with U.S. safety agencies, from 2015–2026 (375 medical device, 56 drug).
What is the most recent Baxter Healthcare Corporation recall?
Baxter Healthcare Corporation recalls Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 Product Code: 3122005 Product, dated Sep 14, 2026. Every Baxter Healthcare Corporation recall is listed on this page, newest first.
Why are Baxter Healthcare Corporation products recalled?
The most common reasons on record: CGMP Deviations (18); IV sets may leak. (16); Potential ability to leak once used for compounding. (6); Potential disconnection of tubing set. (4).
What should I do if I have a recalled Baxter Healthcare Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Baxter Healthcare Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.