Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 — Class II medical device recall Z-1439-2014
Terminated recall by Philips Medical Systems, Inc., reported 2014-04-16, distributed in IN, WA. A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver
| Recall number | Z-1439-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems, Inc., Andover, MA, United States |
| Recall initiated | 2014-03-31 |
| Classified | 2014-04-09 |
| Reported by FDA | 2014-04-16 |
| Terminated | 2015-10-21 |
| Distributed | IN, WA |
| Countries outside the US | CN, DE, FR, GB, IT, MY, PA, SA, TR |
| Quantity | 19 units |
| Reason classes | device malfunction |
| Serial numbers | US11409686, USD1308456, USD1309167, USD1309168, USD1309180, USD1309181, USD1309182, USD1309184, USD1309194, USD1309195, USD1309196, USD1309197, USD1309227, USD1309264, USD1309269, USD1309274, USD1309286, USD1309301, USN1307680 |
| Model numbers | 861290 |
Product
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290, automatic external defibrillator.
Reason for recall
A component on the HeartStart XL+ Therapy Board could malfunction potentially affecting the ability to deliver therapy
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1439-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.