Cardiac Science, Inc. FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9143 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9143
Brand
Cardiac Science, Inc.
Lot Codes / Batch Numbers
The recalled Model 9143 Batteries have the following lot numbers: 7851, 7852, and 7856.
Products Sold
The recalled Model 9143 Batteries have the following lot numbers: 7851, 7852, and 7856.
Cardiac Science, Inc. is recalling FirstSave AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9143 due to Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work.
Recommended Action
Per FDA guidance
A recall letter, dated May 10, 2004, stated that a replacement battery is enclosed with the letter, and instructed consignees to install the new battery in their defibrilllator and return the old battery.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026