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| Issued: 07 November 2007 at 14:00 |
Ref: MDA/2007/085
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Immediate action |
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Action |
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Update |
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Information request |
| Device: Automatic external defibrillator - Welch Allyn AED 20. |
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| Problem: Failure to defibrillate. The manufacturer is recalling a specific batch of these defibrillators to correct a malfunction that prevents or delays the delivery of therapy, which can lead to failure to resuscitate a patient. This recall is in addition to a batch of AED 20 defibrillators recalled in July 2006 to correct a similar malfunction (MDA/2006/047). |
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| Action by: All medical, nursing and paramedical staff, resuscitation training officers, community defibrillation officers and technical staff responsible for the use, maintenance and purchase of these devices. |
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Action:
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Distributed to:
* via CE Bulletin |
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| Contacts: Details of manufacturer contacts and MHRA contacts for technical and clinical aspects. Change of address or removal from address list for Healthcare Commission. |
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| Appendix: Serial numbers of affected devices (in pdf only). |
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Action deadlines for the Safety Alert Broadcast System (SABS)
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Deadline (action underway): 21 November 2007
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Deadline (action complete): 07 December 2007
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