Philips Respironics V680 Ventilator Recall: Risk of Stopping Operation
Philips Respironics V680 Ventilators with certain model numbers may stop working due to an internal electrical circuit issue. Affected units are distributed outside the US and require action.
Use caution until it’s fixed
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.
Contact the company
What happened, in plain English
Philips Respironics V680 Ventilators with specific model numbers have an internal electrical circuit issue that could cause the device to stop working. This poses a risk to users who rely on the ventilator for breathing support. Read more at govinfonow.com/recall/61015-philips-respironics-v680-ventilator-recall-risk-of-stopping-operation.
Source Summary by GovInfoNow · govinfonow.com/recall/61015-philips-respironics-v680-ventilator-recall-risk-of-stopping-operation · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0909-2022
Cite this page
“Philips Respironics V680 Ventilator Recall: Risk of Stopping Operation.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61015-philips-respironics-v680-ventilator-recall-risk-of-stopping-operation. Based on FDA recall #Z-0909-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0909-2022%22&limit=1).
Why it’s dangerous
The ventilator has an internal electrical circuit issue that could cause it to stop working unexpectedly. This might happen during use when the patient needs continuous support, potentially leading to breathing difficulties.
Who’s affected
People using Philips Respironics V680 Ventilators with the specified model numbers are affected. Those who rely on ventilators for medical breathing support are most at risk.
How to tell if you have this one
Check for model numbers including P/N 1103044 (850011) on the ventilator. The product was distributed outside the United States and may have been sold globally.
- Brand
Respironics- Category
Medical device
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Ongoing- Distribution
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, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of Afghanistan, Albania, Algeria, American Samoa, Andorra, Argentina, Australia, Austria, Bahrain, Bangladesh, Belgium, Bhutan, Bolivia, Brazil, Bulgaria, Cambodia, Canada, Chile, China, Colombia, Comoros, Croatia, Cyprus, Czech Republic, Denmark, Ecuador, Egypt, Ethiopia, Finland, France, French Guiana, French Polynesia, Germany, Ghana, Gibraltar, Greece, Guadeloupe, Guam, Guatemala, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, Jersey, Jordan, Kazakhstan, Kenya, Kosovo, Kuwait, Latvia, Lebanon, Libya, Luxembourg, Malaysia, Maldives, Mali, Malta, Martinique, Mauritius, Mexico, Monaco, Mongolia, Morocco, Myanmar, Namibia, Nepal, Netherlands, New Caledonia, New Zealand, Nigeria, Norway, Oman, Pakistan, Palestine, Panama, Paraguay, Peru, Philippines, Poland , Portugal, Puerto Rico, Qatar, R¿union, Romania, Russian Fed., Saudi Arabia, Singapore, Slovenia, South Africa, South Korea, Spain, St. Pier, Miquel., Sweden, Switzerland, Taiwan, Tanzania, Thailand, Turkey, Ukraine, United Kingdom, Utd. Arab. Emir., Venezuela, Vietnam, Wallis, Futuna, Zambia, Japan.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| Z-0907-2022 | Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618, 1076709, 1076716, 1076717, 1137292, DU1053617, U1053617, R1053618, R1076709); All Lots & Serial Numbers. V60 UDI-DI: 00884838009844, 00884838009851, 00884838020054, 00884838025776, 00884838089280, 00884838090996. | 87,138 units |
| Z-0908-2022 | Philips Respironics V60 Plus Ventilator (All Models, including: 1138747, 1137276); All Lots & Serial Numbers | 12,145 units |
| Z-0909-2022 | Philips Respironics V680 Ventilator (All Models, including: P/N 1103044 (850011)), *Distributed outside the United States; All Lots & Serial Numbers ; *Distributed outside the Untied States | — |
What to do — step by step
Check Device Status
Ensure the ventilator is operating normally and not stopping unexpectedly.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 49 states.
FDA distribution: “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, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 58 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-0909-2022 (February 28, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0909-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.