Respironics California, LLC 2022-04-27 Health critical FDA
Health · FDA · Recall #FDA-Z-0909-2022
Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)),… Recall
Issued April 27, 2022 · Respironics California, LLC
In April 2022, Respironics California, LLC recalled the Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)),…, 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
Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some cases could result in the ventilator ceasing to operate.
What you should do
- 1 Stop using Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)),… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Respironics California, LLC 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
- Respironics California, LLC
- Category
- Health
- Recall date
- April 27, 2022
- Units affected
- Not reported
- Sold at
- Worldwide distribution US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA,
- Recall number
- FDA-Z-0909-2022
- Made in
- United States
- Issuing agency
- FDA
In context
- Respironics California, LLC has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 870th Health recall we've logged in 2022.