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Potential Financial Risks for Buyers of Vyaire Medical AirLife Manual Resuscitators

Attention to all hospitals, healthcare facilities, EMS services, and institutions that acquired Vyaire Medical AirLife Manual Resuscitators made in or before 2017: potential financial risks may have been involved.

Recall Alert: Vyaire Medical AirLife Manual Resuscitators

Have you purchased or kept Vyaire AirLife Manual Resuscitators in stock for your hospital, healthcare facility, ambulance service, or organization?

Vyaire Medical has initiated a recall for specific models of its AirLife Manual Resuscitators, associated with a collection of severe injuries and two fatalities.

The presence of faulty resuscitators may have exposed medical facilities and service providers to serious financial liabilities.

Details On The Recall Issued for Vyaire Medical AirLife Manual Resuscitators

Vyaire Medical Inc., in conjunction with the U.S. Food and Drug Administration, has declared a Class I recall on several models of AirLife Manual Resuscitators due to a manufacturing flaw, a defect that could lead to insufficient ventilation in emergencies.

AirLife Manual Resuscitators are single-use bag-valve masks emergency responders use during resuscitation efforts to deliver air into the lungs of patients experiencing breathing difficulties or respiratory arrest.

Approximately 6.6 million units of these devices were manufactured on or before 2017, and they may have been present in hospital stocks, healthcare facilities, and ambulance inventories.

Warning: AirLife Manual Resuscitator Failures Pose Severe Risks

The FDA has received reports of 37 incidents related to AirLife Manual Resuscitators, resulting in two injuries and two tragic deaths.

This recall by Vyaire Medical of the AirLife Manual Resuscitators has been labeled as Class I, indicating the potential for serious injuries or fatalities due to device usage.

The identified flaw in the recalled AirLife units could hinder their ability to deliver sufficient ventilation to patients relying on these devices to prevent oxygen deprivation that could cause severe harm or loss of life.

Beyond the financial burden of replacing recalled inventory, these devices could lead to ongoing treatment failures, potentially exposing healthcare providers to financial risks such as legal action brought by patients who suffered damages.

We encourage hospitals, healthcare facilities, emergency service providers, and other medical institutions that acquired Vyaire Medical AirLife Manual Resuscitators made in or before 2017 to request a free, private case review to potentially qualify for compensation.

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The Recall of Vyaire Medical AirLife Manual Resuscitators Due To Manufacturing Flaws

Hospitals, healthcare facilities, emergency service providers, and medical institutions should have every opportunity to address the manufacturers who left them open to significant financial risk in court and get the compensation and justice they deserve.

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Hospitals, Healthcare Facilities, And EMS Services That Purchased Recalled Vyaire Medical Airlife Manual Resuscitators May Be Eligible For Justice And Compensation

For those exposed to serious financial risks that aren’t satisfied with the manufacturer’s response to your claim, we offer a free, private case review with our experienced legal team to determine the potential compensation value of your case.

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We’ll ask specific questions to understand the situation, the damages, and other vital info to help determine the next steps.

Receive a confidential case evaluation

A qualified legal team led by a personal injury attorney will consider the facts of the case and the potential for compensation.

Have an individual claim filed for compensation

Those that qualify will have an individual claim filed in a court of law for the justice and compensation they deserve.

Our attorneys are experienced in medical and healthcare litigation and know how to encourage stubborn companies to make a real offer of compensation to cover financial exposure, especially any injuries or fatalities resulting from the manufacturer's negligence.

Details On The Recall Issued for Vyaire Medical AirLife Manual Resuscitators

How did the Vyaire Medical AirLife Manual Resuscitator recall begin?

Vyaire Medical Inc., in conjunction with the U.S. Food and Drug Administration declared a Class I recall on several models of AirLife Manual Resuscitators due to a manufacturing flaw with the potential to lead to insufficient ventilation in emergencies.

Models subject to the recall include:

  • AirLife™ Adult Manual Resuscitator, 40″ (1.0 m) Oxygen Reservoir Tubing, Adult Mask, CO2 Detector, 2K8005C2
  • AirLife™ Adult Manual Resuscitator, 40″ (1.0m) Oxygen Reservoir Tubing, Adult Mask, 2K8004
  • AirLife™ Adult Manual Resuscitator, 40″ (1.0m) Oxygen Reservoir Tubing, Adult Mask, 2K8005
  • AirLife™ Adult Manual Resuscitator, 40″ (1.0m) Oxygen Reservoir Tubing, Adult Mask, Expiratory Filter, 2K8005F

Additional models subject to the recall include:

  • AirLife™ Adult Manual Resuscitator, 40″ (1.0m) Oxygen Reservoir Tubing, without Mask, 2K8001
  • AirLife™ Adult Manual Resuscitator, Oxygen Reservoir Bag, Adult Mask, CO2 Detector, 2K8004C2
  • AirLife™ Adult Manual Resuscitator, Oxygen Reservoir Bag, Expiratory Filter, 2K8004F
  • AirLife™ Adult Manual Resuscitator, Oxygen Reservoir Bag, without Mask, 2K8000
  • AirLife™ Adult Manual Resuscitator, Variable Volume Oxygen Reservoir Tubing, Adult Mask, 2K8017

Compensation Begins With A Free Online Case Review

We encourage hospitals, healthcare facilities, emergency service providers, and other medical institutions that acquired Vyaire Medical AirLife Manual Resuscitators made in or before 2017 to request a free, private case review to qualify for potential compensation.

Vyaire Medical AirLife Manual Resuscitator Recall FAQ: Questions About The Recall Details

What are AirLife Manual Resuscitators?

AirLife Manual Resuscitators are single-use bag-valve masks emergency responders use during resuscitation efforts to deliver air into the lungs of patients experiencing breathing difficulties or respiratory arrest.

What damages have resulted from the use of AirLife Manual Resuscitators?

The FDA has received reports of 37 incidents related to AirLife Manual Resuscitators—specifically two injuries and two tragic deaths—directly resulting from their inability to prevent oxygen deprivation in an emergency.

What are any additional damages possible from the use of AirLife Manual Resuscitators?

Beyond the financial burden of replacing recalled inventory, these devices could lead to ongoing treatment failures, potentially exposing healthcare providers to financial risks such as legal action brought by patients who suffered damages.

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