| Product Description | Model/Product Number | Stock Identifiers | Volume | Recall ID |
| LIFEPAK 500 automated external defibrillator. | Part numbers 3005380-000 through 3005380-006 and 3005380-014. | Serial numbers may be obtained from the firm or from Seattle District Recall Coordinator. All battery date codes prior to 0013. | 7,028 units | Z-0886-04 |
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AED Recalls
| Alert Details for #2004050034 (Released 5/05/2004 9:29 EDT) | |
| Description: | LIFEPAK 500 automated external defibrillator. |
|---|---|
| Manufacturer: | Medtronic Physio Control Corp, Redmond, WA |
| Reason: | Potential for batteries to malfunction due to battery cell rupture. |
| Analyst Comments: | Customer Service: (800) 328-2518 |
| Alert Type: | Recall | Source Alert Type: | FDA Recall Class II |
|---|---|---|---|
| Domain: | Biomedical Devices | Source Type: | FDA Enforcement Report |
| Distribution: | Nationwide and Internationally | Source Date: | 5/05/2004 |
| Product Information |