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Help for victims who’ve developed severe infections from the 3M Bair Hugger® warming system used during joint replacement surgeries

Help for victims who’ve developed severe infections from the 3M Bair Hugger® warming system used during joint replacement surgeries

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Consumer remarks against the 3M Bair Hugger® warming system are on the rise.

These comments primarily focus on the infections caused by the 3M Bair Hugger® warming system that led to amputations and deaths.

Victims are developing serious infections after surgeries involving the use of these devices, with some victims losing limbs to infection–plus, many families had a loved one die.

Many of the victims affected had knee and/or hip replacement surgeries resulting in deep-joint infections that were difficult and expensive to treat.

Victims of the most serious 3M Bair Hugger® warming system complications say they developed methicillin-resistant Staphylococcus aureus (MRSA).

MRSA is an antibiotic-resistant infection that can lead to skin infection, sepsis, pneumonia, and bloodstream infections.

Models named as particularly troublesome 3M Bair Hugger® warming systems included:

-Model 500

-Model 505

-Model 750

-Model 775

The letter said the FDA reviewed medical research and data–and the agency also pledged to “actively monitor this situation.”

Since approving the first 3M Bair Hugger® warming system in 1987, the FDA has issued 14 or more additional clearances for changes or newer, improved versions of the devices.

Shield Justice Team believes victims of 3M Bair Hugger® warming system injuries should have every opportunity to address the manufacturers and get the help they deserve.

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