| Product Description | Model/Product Number | Stock Identifiers | Volume | Recall ID |
| a) Powerheart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery | Model 9142 | a) Lot numbers: 7848, 7849, 7850, 7853, 7854, 7855, 7857, 7858, 7859, 7860, 7861, 7863, 7866, 7867, 7868, 7870, 7871, 7872, and 7874 | 4730 batteries total | Z-0990-04 |
| b) FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery | Model 9143 | b) Lot numbers: 7851, 7852, and 7856. | 4730 batteries total | Z-0991-04 |
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AED Recalls
| Alert Details for #2004060122 (Released 6/09/2004 17:38 EDT) | |
| Description: | Automated External Defibrillator batteries |
|---|---|
| Manufacturer: | Cardiac Science, Inc., Irvine, CA |
| Reason: | Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work. |
| Analyst Comments: | Action: Remove from service. For further information contact Cardiac Science at: 1.800.991.5465 (USA ONLY) E-mail: powerheart@cardiacscience.com |
| Alert Type: | Recall URGENT | Source Alert Type: | FDA Recall Class II |
|---|---|---|---|
| Domain: | Biomedical Devices | Source Type: | FDA Enforcement Report |
| Distribution: | Nationwide and Internationally | Source Date: | 6/09/2004 |
| Links: |
|---|
| http://www.fda.gov/opacom/Enforce.html |
| Product Information |