FDA Issues Letter To Pro-Thermoregulation Device Users

The FDA is reminding health care providers that using thermoregulation devices during surgery, including forced air thermoregulating systems, have been demonstrated to result in less bleeding, faster recovery times, and decreased risk of infection for patients. The study was taken up when it was noticed that forced air thermal regulating systems were being avoided by health care providers during surgeries to bypass the chances of increased risk of surgical site infection. Moreover, it reported that the avoidance could lead to the development of adverse health consequences for patients during the post-operative and recovery process. The letter stated clearly that the FDA was unable to identify a consistently reported association between the use of forced air thermal regulating systems and surgical site infection. This is surely a good news for manufacturers of forced air thermal regulating systems like the 3M's Bair Hugger System who is currently facing thousands of lawsuits in the U.S. District Court, District of Minnesota under MDL No. 2666.


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