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RecallsAboutBlog

Baxter Healthcare Corporation

Baxter Healthcare Corporation: 18 recalls listed since January 2026 across FDA; 7 rated high risk.

By year

  • 202618

By agency

  • FDA18

By category

  • Medical Device12
  • Drug6

All recalls (18)

Baxter Likorall Overhead Lifts

Patients are at some risk for injury if a significant fall/drop were to occur due to this issue.

Moderate risk, FDA, , Device defect

Baxter Pro+ MRS Surfaces for VersaCare

PRO+ MRS Surface for Versacare has an error in its UDI label that may lead to incorrect product identification.

Moderate risk, FDA, , Labeling error

Baxter Volara System

Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate.

Moderate risk, FDA, , Contamination

Baxter Novum IQ Syringe Pump

The syringe pump has a software issue that may occur during multi-syringe infusion.

Moderate risk, FDA, , Software defect

Baxter Vancomycin, Insulin, Daptomycin and Other Injections

Vancomycin Injection, USP in 5% Dextrose has CGMP deviations.

Moderate risk, FDA, , Manufacturing problem

Baxter Dextrose Injection

Dextrose Injection contains stainless steel particles that may cause serious health consequences.

High risk, FDA, , Foreign object

Baxter 0.9% Sodium Chloride Injection

0.9% Sodium Chloride Injection contains fiberglass particulate matter that may cause serious health consequences.

High risk, FDA, , Foreign object

Baxter Anticoagulant Sodium Citrate Solution

Anticoagulant Sodium Citrate Solution may contain fiberglass particles that can cause adverse health consequences.

High risk, FDA, , Foreign object

Baxter Duo-Vent Solution Set and Male Luer Lock Adapter

The Baxter Duo-Vent Solution Set and Male Luer Lock Adapter can have air bubbles in the drip chamber and tubing.

High risk, FDA, , Device defect

Baxter Cefazolin in Dextrose Injection

Cefazolin in Dextrose Injection may contain particulate matter, which can cause pulmonary emboli, blood vessel occlusions, and phlebitis.

High risk, FDA, , Foreign object

Hillrom Volara Circuit Kits

There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.

High risk, FDA, , Device defect

Baxter Adapter for Head Positioning

The Adapter for Head Positioning may become loose and move during patient positioning.

Moderate risk, FDA, , Device defect

Exacta Mix Vented Micro-Volume Inlet

Exacta Mix Vented Micro-Volume Inlet tubing sets may contain incorrect filters, causing reduced flow and clinical effects.

Moderate risk, FDA, , Device defect

Baxter Volara Ventilator Adapter Modules

The Blue Ventilator Adapter Module may cause unawareness of oxygen desaturation or barotrauma in home care.

High risk, FDA, , Device defect

Welch Allyn Spot Vision Screener VS100

The Welch Allyn Spot Vision Screener VS100 may have a flickering display that can cause seizures in susceptible people.

Moderate risk, FDA, , Software defect

Spectrum IQ Infusion Pump

The Spectrum IQ Infusion Pump was released without full testing, including occlusion alarm testing.

Moderate risk, FDA, , Device defect

Baxter Sterile Water for Irrigation

Sterile Water for Irrigation contains plastic particles from the bottle rim that can float into the solution.

Moderate risk, FDA, , Foreign object

Baxter SIGMA Spectrum Infusion Pump

The SIGMA Spectrum Infusion Pump has defective grease that may cause over-infusion or free-flow.

Moderate risk, FDA, , Device defect
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