Urgent Field Safety Notice For Astral 100, Astral 150 By Resmed Ltd.
Recall Summary ResMed Ltd. has issued an urgent safety notice for Astral 100 and Astral 150 devices distributed in Germany and the EU. The specific reason for the notice is not detailed in the available information. This is classified as a Class I recall, which is the most serious classification for medical devices.
- Recalling firm
- ResMed Ltd.
- Product
- Astral 100, Astral 150
- Reason
- Urgent Field Safety Notice for Astral 100, Astral 150 by ResMed Ltd.
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-06-25
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/173aee73-ccad-4b02-a29d-bbed1d2a2192