| Product Description | Model/Product Number | Stock Identifiers | Volume | Recall ID |
| HeartStart XL Defibrillator Monitor. | M4735A. | Units with software versions A.02.00 or greater. | 16,736 units total. | Z-1226-03. |
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AED Recalls
| Alert Details for #2003090132 (Released 9/29/2003 0:00 EDT) | |
| Description: | Defibrillator Monitor (Philips Medical Systems). |
|---|---|
| Manufacturer: | Philips Medical Systems, Andover, MA. |
| Reason: | Instructions for use include additional information on configuration for selecting Power on Lead. |
| Alert Type: | Recall | Source Alert Type: | FDA Recall Class II |
|---|---|---|---|
| Domain: | Biomedical Devices | Source Type: | FDA Enforcement Report |
| Distribution: | Nationwide and Internationally. | Source Date: |
| Product Information |