Reported Oct 20, 2021 · Ongoing
Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A
Philips North America LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips North America LLC · 22100 Bothell Everett Hwy · Bothell, WA · 98021-8431
Is this the product you have?
PhilipsHeartStart FR2 + DefibrillatorModel # M3860A and M3861A
- Lot codes and dates
- Model M3860A affected serial numbersA09G-04198 and 510800626
- Model M3861A affected serial numbersA09H-00436 and A07J-03514
- Amount recalled
- 4 units
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
Why it was recalled
Customers were not notified of previous recalls associated with various defibrillator models.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new Philips North America LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.