FDA Device recall Z-1439-2014
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator
- FDA Device
- Class II
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class II recall of Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator by Philips Medical Systems, citing A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1439-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-31 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Philips Medical Systems |
| Distribution | IN, WA |
Product
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Reason
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
Identifiers
| code_info | Serial Numbers: USN1307680 USD1309181 USD1308456 USD1309182 USD1309167 USD1309184 USD1309168 USD1309194 USD1309180…Serial Numbers: USN1307680 USD1309181 USD1308456 USD1309182 USD1309167 USD1309184 USD1309168 USD1309194 USD1309180 USD1309195 USD1309196 USD1309274 USD1309197 USD1309286 USD1309227 USD1309301 USD1309264 US11409686 USD1309269 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1439-2014%22
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