Ventilator Correction

2 recalls on record · Last recall: Jul 31, 2026

Read the history in context

Records, not a safety rating.

Recall counts do not account for sales volume, exposure or differences in reporting. Agency records can overlap. A low count does not establish that a brand or product is safe.

View source coverage →

Severity Breakdown

Class I — Serious

Class II — Moderate

Class III — Low Risk

Unclassified

Recall Timeline

FDAJul 31, 2026

Ventilator Correction: Resmed Issues Correction for Astral Ventilator

Failure of an electrical component in certain Astral ventilators may cause an interruption or failure in therapy which may result in serious injury or death.

FDAMay 28, 2026

Ventilator Correction: Philips Issues Correction for Trilogy Evo Platform Ventilators

Philips Trilogy Evo Ventilators may not function as intended if used with certain nebulizers.

Track Ventilator Correction recalls automatically

Get an alert when a matching Ventilator Correction recall turns up.

Start Free Trial