Zoll Lifecor Corporation Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit assembly (PCA) within the monitor. The LifeVest is indicated for adult patients who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit assembly (PCA) within the monitor. The LifeVest is indicated for adult patients who are at risk for sudden cardiac arrest and are not candidates for or refuse an implantable defibrillator.
Brand
Zoll Lifecor Corporation
Lot Codes / Batch Numbers
model numbers WCD3000 and WCD3100
Products Sold
model numbers WCD3000 and WCD3100
Zoll Lifecor Corporation is recalling Monitor portion of the LifeVest device - specifically the Defibrillator printed circuit assembly (PC due to The charging circuit will not shut down properly.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The charging circuit will not shut down properly.
Recommended Action
Per FDA guidance
Physicians with active patients were notified of the product removal by letter via first-class mail dated 10/21/2008. The letter describes the problem and the potential risk. For additional information, contact ZOLL Lifecor Corporation at 1.800.543.3267.
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