[Recalled] Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 Product Usage: The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. Th
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Philips HeartStart MRx monitor/defibrillators Models: M3535A, M3536A, M3536M4, M3536M5, and M3536M6 Product Usage: The Heartstart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the opera |
|---|---|
| Brand / manufacturer | Philips Healthcare Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1896-2012 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 20 June 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: HeartStart MRx Unexpected Pads/Paddles ECG Failure
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Philips Healthcare Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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