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FDA Medical Device Recalls (openFDA)

Cardiac Science, Inc.: Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9142

Recall number
Z-0990-04
Recalling firm
Cardiac Science, Inc.
Product
Power Heart AED G3 Automated External Defibrillator IntelliSense (Lithium) Battery, Model 9142
Status
Terminated
Initiated
2004-05-04
Posted
2004-07-20
Terminated
2005-11-18
Reason
Some of the recalled defibrillator batteries contain an incorrect fuse which could open resulting in a defibrillator which will not work.
Root cause
Other
Action
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.
Quantity
not on file
Distribution
The batteries were distributed with the defibrillators nationwide in the United States and to foreign consignees in Europe, Asia, Latin America, the Middle East and Africa.
Lot, serial or model codes
The recalled Model 9142 Batteries have the following lot numbers: 7848, 7849, 7850, 7853, 7854, 7855, 7857, 7858, 7859, 7860, 7861, 7863, 7866, 7867, 7868, 7870, 7871, 7872, and 7874.
510(k) numbers
["K031987"]
PMA numbers
not on file
Product code
MKJ
Firm FEI
2112020
Firm city
Irvine
Firm state
CA
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

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Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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