HeartSine 350P US Device, US English (American Airlines) - 2 Min CPR
HeartSine 350P US Device, US English (American Airlines) - 2 Min CPR
Lower-risk recall
Due to a damaged (over stretched) membrane tail that causes an intermittent fault.
What happened, in plain English
HeartSine 350P US Device, US English (American Airlines) - 2 Min CPR Read more at govinfonow.com/recall/1009728-heartsine-350p-us-device-us-english-american-airlines-2-min.
Source Summary by GovInfoNow · govinfonow.com/recall/1009728-heartsine-350p-us-device-us-english-american-airlines-2-min · Updated September 23, 2026 · FDA enforcement record: FDA #Z-3120-2026
Cite this page
“HeartSine 350P US Device, US English (American Airlines) - 2 Min CPR.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/1009728-heartsine-350p-us-device-us-english-american-airlines-2-min. Based on FDA recall #Z-3120-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3120-2026%22&limit=1).
Why it’s dangerous
This is a low risk item. The device is a standard defibrillator used by American Airlines for CPR training. It is not a security threat.
Who’s affected
American Airlines
How to tell if you have this one
This device is a standard defibrillator used for CPR training. It is not a security threat.
- Brand
HeartSine- Category
Medical device
What to do — step by step
1
The device is a standard defibrillator used by American Airlines for CPR training. It is not a security threat.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 37 states.
FDA distribution: “Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME MI, MN, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SD,TN, TX, UT, VA, WA, WI, WV and WY. The countries of…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Alaska, Arizona, California, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Maine, Maryland, Massachusetts, Michigan, Minnesota, Nevada, New Jersey, New Mexico, New York, North Carolina, Ohio, Oklahoma, Oregon, Pennsylvania, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin, Wyoming.
Recall timeline
FDA published this recall 51 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
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-3120-2026 (July 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3120-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 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.