# FDA device recall: Resmed Astral 100/150    Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilator

> recall · VERIFIED · 2026-06-25

Firm: ResMed Ltd. · Class I · Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.

- Company: ResMed Ltd.
- Sector: medical devices
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.