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Terminated

DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor.

FDA Recall Z-0971-04 · Posted 2004-07-20

Recalling FirmMedtronic Physio Control Corp
Recall StatusTerminated
Product CodeLDD
Date Initiated2004-05-05
Date Terminated2005-01-06
Product Quantity1689

Reason for Recall

The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.

Firm Action

On 5/5/04 the firm issued a letter to consignees advising of the problem and that a service representative will contact them regarding replacement of the DC Power Adapter.

Root Cause

Other

Distribution Pattern

The firm distributed devices to medical facilities, fire departments (first responders).

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K012274MEDTRONIC PHYSIO-CONTROL LIFEPAK 20 DEFIBRILLATOR/MONITOR/PACEMAKERMedtronic Physio-Control Corp. · 2002-02-05

Official Source

View FDA Recall →

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

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