Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The… — Class II medical device recall Z-0871-2013
Terminated recall by Philips Healthcare Inc., reported 2013-02-27, distributed nationwide. Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use
| Recall number | Z-0871-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Healthcare Inc., Andover, MA, United States |
| Recall initiated | 2013-01-28 |
| Classified | 2013-02-21 |
| Reported by FDA | 2013-02-27 |
| Terminated | 2020-09-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BE, BG, BH, CH, CO, CY, CZ, DE, DK, DO, DZ, EE, EG, ES, FI, FR, GB, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, KE, KR, KW, LB, LK, LT, LV, MA, MT, MY, NL, NO, NZ, OM, PL, PT, RO, SA, SE, SG, SI, SK, TH, TN, TR, TT, VN, ZA |
| Quantity | 3,785 units |
| Model numbers | 861290 |
Product
Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation
Reason for recall
Philips HeartStart XL+ Defibrillator/Monitor may become locked out of clinical use
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-0871-2013. 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.