| Product Description | Model/Product Number | Stock Identifiers | Volume | Recall ID |
| LIFEPAK 12 defibrillator/monitor | Part numbers VLP12, UVLP12, EVLP12, DVLP12, AVLP12, and any of these may have five to eight digits after the base number. Serial numbers can be obtained from the firm or FDA's Seattle District Recall Coordinator. | 2,885 devices. | Z-0938-04 |
 |
AED Recalls
| Alert Details for #2004050294 (Released 5/24/2004 15:52 EDT) | |
| Description: | UPDATED ALERT: LIFEPAK 12 defibrillator/monitor. |
|---|---|
| Manufacturer: | Medtronic Physio Control Corp, Redmond, WA |
| Reason: | Potential for display to go blank due to an electrical component that may fail due to mechanical shock of vibration of the defibrillator. |
| Analyst Comments: | This recall is an update of RASMAS alert #2004040147. |
| Alert Type: | Recall | Source Alert Type: | FDA Recall Class II |
|---|---|---|---|
| Domain: | Biomedical Devices | Source Type: | FDA Enforcement Report |
| Distribution: | Nationwide and Internationally | Source Date: | 5/12/2004 |
| Links: |
|---|
| http://www.fda.gov/opacom/Enforce.html |
| Product Information |