Baxter Healthcare Corporation Recalls
36 recalls on record in the United States
Baxter Healthcare Corporation recalls Blue Ventilator Adapter Module, single-patient use circuit,
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 decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use.
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Baxter Healthcare Corporation recalls Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spo
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
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Baxter Healthcare Corporation recalls Brand Name: Exacta Mix Product Name: Vented Micro-Volume In
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 efficiency, incomplete or slower transfers of ingredients, or system alarms. This issue may lead to clinical effects such as electrolyte imbalance, metabolic instability, delayed recovery, etc.
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Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use C
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 oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.
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Baxter Healthcare Corporation recalls Adapter for Head Positioning, Model/Catalog Number: 1739994,
The Adapter for Head Positioning accessory may become loose during patient positioning and unintentionally move when used in conjunction with the side rails of the Upper Back Section H V U component on Baxter operating tables.
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Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use
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 oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.
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Baxter Healthcare Corporation recalls Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circ
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 oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.
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Baxter Healthcare Corporation recalls Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Cir
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 oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.
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Baxter Healthcare Corporation recalls Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Pro
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 position.
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Baxter Healthcare Corporation recalls Cefazolin in Dextrose, Injection, USP, 2g / 100mL (20mg / mL
Presence of Particulate Matter
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Baxter Healthcare Corporation recalls Clindamycin Injection USP in 5% Dextrose, 900 mg per 50 mL (
CGMP Deviations
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Baxter Healthcare Corporation recalls Vasopressin, in 0.9% Sodium Chloride Injection, 20 units per
CGMP Deviations
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Baxter Healthcare Corporation recalls Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per
CGMP Deviations
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Baxter Healthcare Corporation recalls CARDENE IV (Nicardipine Hydrochloride) in 0.83% Sodium Chlor
CGMP Deviations
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Baxter Healthcare Corporation recalls Pantoprazole Sodium in 0.9% Sodium Chloride Injection, 80 mg
CGMP Deviations
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Baxter Healthcare Corporation recalls Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50
CGMP Deviations
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Baxter Healthcare Corporation recalls Nexterone (amiodarone HCI), 360 mg/200 mL (1.8 mg/mL) in GAL
CGMP Deviations
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Baxter Healthcare Corporation recalls Clindamycin Injection USP in 5% Dextrose, 600 mg per 50 mL (
CGMP Deviations
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Baxter Healthcare Corporation recalls Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Inject
CGMP Deviations
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Baxter Healthcare Corporation recalls Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 m
CGMP Deviations
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Baxter Healthcare Corporation recalls MYXREDLIN, Insulin Human in 0.9% Sodium Chloride Injection,
CGMP Deviations
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Baxter Healthcare Corporation recalls Famotidine Injection in Sodium Chloride Injection, 20 mg, 50
CGMP Deviations
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Baxter Healthcare Corporation recalls Vancomycin Injection, USP, in 0.9% Sodium Chloride, 1g per 2
CGMP Deviations
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Baxter Healthcare Corporation recalls Vasopressin, in 0.9% Sodium Chloride Injection, 40 units per
CGMP Deviations
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Baxter Healthcare Corporation recalls Clindamycin Injection USP in 5% Dextrose, 900 mg/50 mL (18 m
CGMP Deviations
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Baxter Healthcare Corporation recalls Vancomycin Injection, USP in 5% Dextrose, 1 g per 200mL (5 m
CGMP Deviations
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Baxter Healthcare Corporation recalls Clindamycin Phosphate in 0.9% Sodium Chloride Injection, 600
CGMP Deviations
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Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS
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 (VTBI) remains.
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Baxter Healthcare Corporation recalls Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXU
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 (VTBI) remains.
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Baxter Healthcare Corporation recalls Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
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Showing 30 of 36 recalls. See all →