Philips Respironics, Inc. 2024-05-29 Health critical FDA
Health · FDA · Recall #FDA-Z-1812-2024
BiPAP V30 Auto Ventilator, Part Number 1111178 Recall
Issued May 29, 2024 · Philips Respironics, Inc.
In May 2024, Philips Respironics, Inc. recalled the BiPAP V30 Auto Ventilator, Part Number 1111178, 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 devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.
What you should do
- 1 Stop using BiPAP V30 Auto Ventilator, Part Number 1111178 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
- May 29, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution. US Nationwide including PR and GU; Austria, Belgium, Cyprus, Czech Republic, Denmark, France, Germany, Hungary, Ital
- Recall number
- FDA-Z-1812-2024
- 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.