Update On Product Correction A40/30 Bipap Series
Philips is recalling A30 and A40 series BiPAP devices across Australia due to ongoing problems with the devices. The company is contacting affected users to arrange replacements or discuss other options. This is a Class I recall, which indicates a serious safety issue.
- Product
- Due to ongoing problems with their A30 and A40 series BiPAP devices, Philips is now contacting those affected to organise replacement devices or discuss alternative options.
- Reason
- Due to ongoing problems with their A30 and A40 series BiPAP devices, Philips is now contacting those affected to organise replacement devices or discuss alternative options.
- Classification
- Class I
- Category
- consumer product recall
- Country
- Australia
- Agency
- Therapeutic Goods Administration
- Recall date
- 2025-07-03
- Status
- Ongoing
- Distribution
- Australia-wide
Official recall notice from Therapeutic Goods Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/9cab06fc-a600-489b-8b92-de3edd394f37