Respironics California, Inc., a division of Philips Healthcare announced
today that it has completed notifying its United States customers of a voluntary recall of
116 Respironics V60 Ventilators in the United States and has confirmed that 33 have
already been updated. The recall was initiated on July 31, 2012 to address a
manufacturing issue that may have affected these ventilators.
This is a summary of a recall issued by the Food and Drug Administration (FDA). The link below will take you to the original recall press release containing complete information, including instructions about what to do if you are affected by this recall.