Zoll Medical Corporation Zoll M Series Automated Defibrillator (AED) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Zoll M Series Automated Defibrillator (AED)
Brand
Zoll Medical Corporation
Lot Codes / Batch Numbers
Software Versions below 34.00
Products Sold
Software Versions below 34.00
Zoll Medical Corporation is recalling Zoll M Series Automated Defibrillator (AED) due to Visual Sreen display and audible prompt may not advise to 'Press Shock'. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Visual Sreen display and audible prompt may not advise to 'Press Shock'
Recommended Action
Per FDA guidance
Zoll Medical notified consignees by letter on 8/2/04 via Certified Mail. Users are advised of the problem and the softtware upgrade.
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