| Product Description | Model/Product Number | Stock Identifiers | Volume | Recall ID |
| LIFEPAK 20 Defbrillator/Monitor | Part numbers: 3202487-xxxd and 3202488-xxx | Various, noncontiguous serial numbers. | 3,924 units total. | Z-0984-05 |
 |
AED Recalls
| Alert Details for #2005070424 (Released 7/20/2005 17:50 EDT) | |
| Description: | Update to RASMAS Alert #2005060180 of 6/24/05 (One additional part number) LIFEPAK 20 Defbrillator/Monitor. |
|---|---|
| Manufacturer: | Medtronic Emergency Response Systems, Inc., Redmond, WA |
| Reason: | The device defibrillator may not operate if the device is turned on during an AC loss alert. |
| Analyst Comments: | Confirm receipt of manufacturer's notice dated June 17, 2005. If this device is in your inventory, please contact Medtronic Emergency Response Systems, Inc., 1-800-442-1142. http://www.medtronic-ers.com/index.cfm |
| Alert Type: | Recall | Source Alert Type: | FDA Recall Class II |
|---|---|---|---|
| Domain: | Biomedical Devices | Source Type: | FDA Enforcement Report |
| Distribution: | Nationwide and Internationally | Source Date: | 7/20/2005 |
| Links: |
|---|
| http://www.fda.gov/po/enforceindex/2005enforce.html |
| Product Information |