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  1. #1
    Deal GURU
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    Default RECALL OF LIFEPAK CR Plus and LIFEPAK EXPRESS AUTOMATED DEFIBRILATORS

    Product Description The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators.

    Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.

    Recall Number Z-1082-2013

    Classification Class II


    Product Distributed Qty 54,197 units in US and 78,627 units internationally (total 132, 824 units) -> Please refer to the FDA Enforcement Report for the week of April17, 2013 for specific serial numbers

    Reason For Recall LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.

    Event Detail

    Event Id 64427

    Product Type Devices

    Status Ongoing

    Recalling Firm Physio Control, Inc., Redmond, WA, USA

    Voluntary / Mandated
    Voluntary: Firm Initiated

    Recall Initiation Date 2013-02-08

    Initial Firm Notification of Consignee or Public
    Letter

    Distribution Pattern Worldwide Distribution

  2. #2
    Deal GURU
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    Default Re: RECALL OF LIFEPAK CR Plus and LIFEPAK EXPRESS AUTOMATED DEFIBRILATORS

    I struggled with whether or not this recall might affect the readers of this forum before posting.

    LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) may be used by AED Certification courses, EMT classes, Health professions training courses or by local government in first response multiple casualty disaster training.

    I have seen them in airports, and workplaces.

    If you have one in your workplace or training center help spread the word and have the battery replaced. These devices save lives, but only if they are charged.

 

 

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