Baxter Healthcare Corporation recalls
39 recalls.
- Likorall Overhead Lifts Product Code: 3121001 Product Description: LIKORALL 200 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported October 21, 2026 · Potential issue involving motor shaft breakage combined with reduced performance of the Single Fault Safety (SFS) system may lead to instances where the lift... - PRO+ 40" MRS SURFACE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - PRO+ 36" MRS SURFACE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - PRO+ MRS SURFACE FOR VERSACARE recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the approved... - Brand Name: VOLARA System Product Name: VOLARA recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 30, 2026 · Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to firm and... - Dextrose Injection recall (Baxter Healthcare Corporation)
DrugClass IReported September 16, 2026 · Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution. - 0.9% Sodium Chloride Injection USP 500 mL recall (Baxter Healthcare Corporation)
DrugClass IReported September 9, 2026 · Presence of particulate matter: Particulates identified as fiberglass - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Phosphate in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Nexterone recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - CARDENE IV recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Pantoprazole Sodium in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vasopressin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Famotidine Injection in Sodium Chloride Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Clindamycin Injection USP in 5% Dextrose recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Daptomycin recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - MYXREDLIN recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Vancomycin Injection recall (Baxter Healthcare Corporation)
DrugClass IIReported September 9, 2026 · CGMP Deviations - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Baxter Novum IQ Syringe Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported September 9, 2026 · A software issue that may occur during a Volume/Time (VOT) multi-syringe infusion when a syringe reaches empty and is replaced while a Volume To Be Infused... - Cefazolin in Dextrose recall (Baxter Healthcare Corporation)
DrugClass IReported August 19, 2026 · Presence of Particulate Matter - Baxter Duo-Vent Solution Set and Male Luer Lock Adapter recall (Baxter Healthcare Corporation)
Medical deviceClass IReported August 19, 2026 · Baxter received customer reports of air bubbles in the drip chamber and tubing when a pressure cuff is in use or when the tubing is flushed at the fully open... - Adapter for Head Positioning recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported July 8, 2026 · The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA P.CIRCUIT 5KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported June 10, 2026 · Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow... - Blue Ventilator Adapter Module recall (Baxter Healthcare Corporation)
Medical deviceClass IReported April 8, 2026 · Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible... - Brand Name: Welch Allyn recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported March 25, 2026 · Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible... - Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 ... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported February 25, 2026 · Pumps were released without full testing being performed, including occlusion alarm testing. - Sterile Water for Irrigation recall (Baxter Healthcare Corporation)
DrugClass IIReported February 4, 2026 · Presence of particulate matter: plastic particles from the bottle rim were observed floating into the solution - SIGMA Spectrum Infusion Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported January 28, 2026 · Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective...