Replacement process

The manufacturer Philips is proceeding to replace the devices affected by the recall it launched on June 14.

The following models has begun being replaced by Philips:

• DreamStation1 PRO
• DreamStation1 Auto
• DreamStation1 Expert
• Bipap Auto DreamStation1
• Bipap AVAPS/ST DreamStation1
• One Pro Series 50 system
• One Auto 50 series system
• One Pro 60 series system
• One Auto series 60 system

Details: 

1. DreamStation 1 devices are being replaced with a DreamStation 2 or a refurbished DreamStation 1 featuring new sound-absorbing foam approved by the Food and Drug Administration (FDA).
2. Philips determines which devices are replaced with a DreamStation 2 and which ones are replaced with a refurbished DreamStation 1. Biron is not informed of Philips’ decision-making process in this regard.
3. The devices will be replaced in the order in which they were registered for recall.

The patients concerned will receive a letter inviting them to proceed with the exchange, along with instructions for doing so. 

IMPORTANT: Philips has not yet provided information on when it will exchange, replace or repair the other affected devices. When we receive instructions in this regard, we will contact the patients concerned.