Philips Respironics, Inc. 2024-04-24 Health critical FDA
Health · FDA · Recall #FDA-Z-1505-2024
Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for… Recall
Issued April 24, 2024 · Philips Respironics, Inc.
In April 2024, Philips Respironics, Inc. recalled the Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential for sudden loss of ventilation due to Battery Depleted or Loss of Power alarm while unit has sufficient power.
What you should do
- 1 Stop using Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips Respironics, Inc. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Philips Respironics, Inc.
- Category
- Health
- Recall date
- April 24, 2024
- Units affected
- Not reported
- Sold at
- Domestic: Nationwide Distribution; Foreign: AE, AR, AT, AU, BD, BE, BG, BO, BR, BS, CA, CH, CL, CN, CO, CZ, DE, DK, DZ, EC, EE, EG, ES, FI,
- Recall number
- FDA-Z-1505-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips Respironics, Inc. has 7 recalls in our database, including 7 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.