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Bair Hugger FAW Device Lawsuits


The manufacturers of the Bair Hugger forced air warming (FAW) device, used to supply warm air to patients during surgery, are facing multiple lawsuits after use of the device has been linked to an increased risk of bacterial infection to patients.

Originally intended to help regulate body temperature during surgery to prevent hypothermia, the device has been widely used in hospitals throughout the country since its release in 1987. Now, even the inventor of the FAW device, Dr. Scott D. Augustine, is warning hospitals to cease use during certain surgical procedures because of potential risks. Among those especially vulnerable to complications from the device are joint replacement patients and those receiving artificial heart valves.

For a complimentary Bair Hugger case evaluation, call (678) 394-3531. Schneider Hammers is currently reviewing cases from victims nationwide.

The Bair Hugger FAW Device Can Cause Patients to Develop Serious Infections

The Bair Hugger device is a blanket that is placed over patients during surgical procedures to keep the patient warm during surgery. This is supposed to decrease the risk of complications associated with even mild hypothermia, which can lead to blood loss, infections, and prolonged hospital stays. Unfortunately, however, use of the device has been shown to actually increase a patient’s risk of exposure to bacteria, leading to a number of serious and highly contagious infections including Methicillin-resistant Staphylococcus aureus (MRSA). These infections can be highly difficult to treat and, in some cases, have even led to additional surgeries and/or limb amputations after a patient has contracted the bacteria.

The Bair Hugger device is still in use in over 80 percent of U.S. hospitals, with 50,000 units throughout the country. Current lawsuits allege that there have been no efforts to sufficiently warn healthcare providers of the dangers it poses, nor have there been any redesigns to make the device safe to use. In addition, the Bair Hugger FAW has been found to remove less than 65 percent of airborne particles .30 microns or larger when the current High-Efficiency Particulate Air (HEPA) standards require all air-filtration devices to remove 99.97 percent of all airborne particles.

Call Our Award-Winning Atlanta Product Liability Lawyers for a FREE Case Review

If you or a loved one have had a joint replacement or other implant surgery where the Bair Hugger FAW device was used, you may have cause for legal action. We encourage you to get in touch with an Atlanta personal injury lawyer at Schneider Hammers if you experienced a serious infection within one year of your procedure. You may be entitled to pursue compensation in a lawsuit against the maker of this dangerous medical device.

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Schedule a complimentary, no obligation consultation with a member of our team to learn more about how we can help: (678) 394-3531.

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