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Terminated

Zoll M Series Automated Defibrillator (AED)

FDA Recall Z-1472-04 · Posted 2004-09-17

Recalling FirmZoll Medical Corporation
Recall StatusTerminated
Product CodeMKT
Date Initiated2004-08-02
Date Terminated2017-02-13
Product Quantity5649 units

Reason for Recall

Visual Sreen display and audible prompt may not advise to 'Press Shock'

Firm Action

Zoll Medical notified consignees by letter on 8/2/04 via Certified Mail. Users are advised of the problem and the softtware upgrade.

Root Cause

Other

Distribution Pattern

Nationwide

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K010257ZOLL M SERIESZoll Medical Corp · 2001-02-28

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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