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Philips Respironics, Inc. Updates Use Instructions for BiPAP V30, BiPAP A30, BiPAP A40 Due to Interruptions and/or Loss of Therapy

Philips Respironics, Inc. is updating the use instructions for V30, A30, and A40 ventilators due to a failure in the Ventilator Inoperative alarm, which can cause therapy interruption or loss.

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death if you continue to use it without following the updated instructions. 

Questions?

If you have questions about this recall, contact Philips Respironics, Inc. at 1-800-345-6443, prompts 4, 5 or email at respironics.clinical@philips.com.