Every recall we track for Baxter Healthcare Corporation — 405 in all — plus the complaints and injury reports the public filed about them.
Baxter Healthcare recalls Cefazolin injection bags with particulate matter. Affected units contain lot # LD175708, expiring Feb 2027. Consumers should contact Baxter for details.
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.
Hillrom recalls Volara P.Circuit 5Kit (REF M08270) due to air and medication leaks causing oxygen drops. Patients may receive ineffective treatment if nebulizer cup isn't locked properly after adding medication.
Hillrom recalls VOLARA System circuit kits with air and medication leaks that may cause oxygen drops. Affected units sold from 4/28/2025 onward; fix by ensuring nebulizer cup locks properly.
Hillrom recalls VOLARA System P.CIRCUIT 5KIT AC (model REF M08474) due to oxygen leakage during therapy. This may cause low oxygen levels and ineffective treatment. Affected units were distributed starting April 28, 2025.
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.
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.
Baxter recalls head positioning adapter model 1739994 for possible loosening when used with operating table side rails, risking unintended movement during patient positioning.
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.
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 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.
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 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.
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.
Baxter Healthcare Corporation product codes and serial numbers for various medical devices and equipment.
Baxter recalls non-vented CLEARLINK IV solution sets that may leak, risking infection. Affected units have specific product codes and lot numbers. Stop using immediately to prevent contamination.
Baxter Healthcare recalls CLEARLINK SYSTEM EXTENSION SETs with potential leakage. This could cause IV fluids to leak, potentially leading to complications. Affected units have specific product codes and lot numbers.
Baxter recalls non-vented CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. Leaks may cause infections during IV treatments. Affected units have specific product codes and lot numbers.
Baxter recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets with 0.2 micron filters due to potential leaks that could cause infection during IV therapy. Affected units include specific lot numbers and product codes.
Baxter Healthcare recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. Affected units have specific product codes and lot numbers. Stop using immediately to prevent IV leaks.
Baxter recalls specific CLEARLINK IV extension sets with potential leakage. Affected units have product code 2H860: R25C26154 and R25C27079 lot numbers. Stop using if leaks occur.
Baxter Healthcare recalls CLEARLINK SYSTEM EXTENSION SETs with potential leakage. Affected units have specific product codes and lot numbers. Stop using if leaking to prevent IV complications.
Baxter recalls specific IV solution sets that may leak, causing potential complications. Affected units include model 2C6255 with lot numbers R25C26161 and R25D01031.
Baxter recalls specific CLEARLINK System Paclitaxel Sets due to potential leaks. Affected units have polyethylene tubing and specific lot numbers. Stop using immediately to prevent medication errors.
Baxter recalls CLEARLINK SYSTEM NON-DEHP CONTINU-FLO SOLN SETs with possible leaks. Leaks may cause infection. Affected units have Product Code 2H8519 and Lot numbers R25C08147.
Baxter Healthcare recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets due to potential leaks that could cause infection. Affected units have specific product codes and lot numbers. Stop using immediately to prevent health risks.
Baxter recalls certain CLEARLINK SYSTEM CONTINU-FLO Solution Sets due to potential leaks. This could cause IV fluids to leak from the tubing, potentially leading to complications during medical treatments.
Baxter Healthcare recalls CLEARLINK SYSTEM EXTENSION SETs with potential leakage. This could cause IV fluid to leak from the patient's IV line, risking infection or discomfort. Affected units have specific product codes and lot numbers.
Baxter recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. This recall addresses a risk of IV fluid leaks that could cause complications during medical treatments.
Baxter recalls CLEARLINK SYSTEM CONTINU-FLO Solution Sets with potential leakage. Affected units have specific lot numbers and product codes. Stop using if leaks occur to prevent infection risks.
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 Healthcare recalls acetaminophen injection with discoloration risk. Check product details to determine if affected. Stop using if discoloration observed.
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 recalls Novum IQ Syringe Pumps (Product Code 40700BAX) due to software issues that may cause blank run screens or false motor errors. Affected units should be checked for serial numbers.
Baxter recalls Novum IQ Large Volume Pumps due to software issues that may cause blank run screens or false motor errors, affecting patients receiving IV treatments.
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 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.
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.
Baxter recalls Spectrum Infusion Pump V8 Model 35700BAX2 with incorrect software version. Affected units may have safety risks; contact for repair or replacement.
Baxter recalls Spectrum Infusion Pump V6 Model 35700BAX with incorrect software version. Affected units may have safety risks; contact Baxter for details.
Hillrom recalls Q-Link 13 components (Product Code 3156509) used with specific mobile patient lifts due to risk of false latching causing patient falls. Affected units were manufactured between August 2013 and February 2025.
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.
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.
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 Healthcare recalls Affinity 4 Birthing Beds with specific product codes due to potential signal wire crimps causing loss of bed lowering function.
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.
Baxter Healthcare recalls Welch Allyn Life2000 Ventilation systems with specific product codes due to a discovered cybersecurity vulnerability. Affected units may have security risks.
Baxter Healthcare recalls Welch Allyn Life2000 Compressors with specific product codes due to a cybersecurity vulnerability found during internal testing.
Baxter Healthcare recalls Welch Allyn CP150 electrocardiographs with third-party batteries that may cause fires. Check serial numbers listed to determine if your device is affected.
Baxter Healthcare recalls Welch Allyn CONNEX Accessory Power Management Stands with third-party batteries that can cause fires. Affected units have specific serial numbers and product codes.
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.
Recall of Welch Allyn Connex Integrated Wall System blood pressure cuffs with undeclared natural rubber bands in packaging. Affected units include specific product codes and lot numbers. No action needed for safe use.
Welch Allyn recalls Green Series 777 Wall System blood pressure cuffs with undeclared natural rubber bands in packaging that could cause allergic reactions. Affected units include specific model numbers and lot numbers.
Baxter Healthcare recalls Welch Allyn Spot Vital Signs 4400 blood pressure cuffs with undeclared natural rubber bands in packaging that could cause injury during use.
Baxter Healthcare recalls Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits with undeclared natural rubber bands in packaging that could cause injury during use.
Recall of Welch Allyn DuraShock blood pressure cuff sets with undeclared natural rubber bands in packaging. Affected models include specific product codes and lot numbers. Consumers should check their units for the listed identifiers.
Welch Allyn recalls certain Connex Spot Monitor blood pressure cuffs due to undeclared natural rubber bands in packaging that could cause injury during use.
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.
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.
Baxter Healthcare recalls TruSystem 7500 mobile columns with software issue causing upper back section to become unadjustable when emergency mode is enabled. Affected units have specific serial numbers and were sold until November 2024.
