Philips Healthcare Inc. Recall: Philips HeartStart XL+ Defibrillator/Monitor Model number:
Philips Healthcare Inc. Recall: Philips HeartStart XL+ Defibrillator/Monitor Model number: is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Healthcare Inc.; Product: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hos
| Recalling firm | Philips Healthcare Inc. |
|---|---|
| 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 |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - USA (nationwide) and Internationally to ALGERIA, ANGOLA, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, BULGARIA, COLOMBIA, CROATIA (LOCAL NAME HYVATSKA), CYPRUS, CZECH REPUBLIC, DENMARK, DOMINICAN REPUBLIC, EGYPT, ESTONIA, FINLAND, FRANCE, GABON, GERMANY, HONG KONG, HUNGARY, ICELAND |
| Recall initiated | 20130128 |
| Recall number | Z-0871-2013 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
Try RecallGuard →