Reported Apr 16, 2014 · Terminated
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Philips Medical Systems, Inc.
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 Medical Systems, Inc. · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
- Philips HeartStart XL+
- Defibrillator/Monitor Model number861290, automatic external defibrillator
- Lot codes and dates
- Serial Numbers
USN1307680USD1309181USD1308456USD1309182USD1309167USD1309184USD1309168USD1309194USD1309180USD1309195USD1309196USD1309274USD1309197USD1309286USD1309227USD1309301USD1309264US11409686USD1309269
- Serial Numbers
- Amount recalled
- 19 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
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 Medical Systems, Inc. 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.