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Medtronic Lifepak Cr Plus User Manual Guide
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![Lifepak Lifepak](/uploads/1/2/6/3/126391539/669029595.jpg)
The Physio-Control LIFEPAK CR® Plus defibrillator combines best-in-class technology with the simplicity and portability required for use by the general public in a sudden cardiac arrest emergency. Windows 8.1. It puts the advantages and advanced technology emergency medical professionals have come to trust and rely on squarely in the hands of anyone ready to save a life in the event. View and Download Medtronic LIFEPAK 500 instructor manual online. LIFEPAK 500 Medical Equipment pdf manual download. Medical Equipment Medtronic MiniMed 508 User Manual. Insulin pump (77 pages) Medical Equipment Medtronic 5392 Technical Manual. Dual chamber temporary external pacemaker (106 pages) Medical Equipment Medtronic 5392 User. LIFEPAK® CR Plus Defibrillator User’s Checklist CHARGE-PAK™ charger and electrode pads need to be replaced ORCHARGE-PAK charger is not installed Service needed Internal battery not fully charged Notify:. Use AED if needed. Immediately notify:.
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Employee error | |||||||||||||||||||||||||||
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On 8/28/08 the firm began contacting consignees by telephone and stating that the LIFEPAK CR Plus defibrillators were discomfiture as semi-automatic, and that a responder is unable to press the shock button to deliver therapy when instructed by the AED voice prompt because the shock button is covered and not visible. The consignee was instructed that the unit(s) would be replaced immediately. This phone contact was followed by a letter flagged 'URGENT - MEDICAL DEVICE RECALL' dated August 2008 that was f axed or e-mailed the same day. The letter repeated the information provided in the telephone contact and stated to 'Immediately perform one of the following actions: Remove the affected AEDs from service or Remove and discard the shock button cover (see enclosed illustration). Enclosed with the letter is an illustration providing instructions for removal of the auto shock button cover. Customer notification was completed by 9/2/08. | |||||||||||||||||||||||||||
249 units | |||||||||||||||||||||||||||
Worldwide Distribution including USA, and countries of Canada, Germany, and Hong Kong. | |||||||||||||||||||||||||||
TPLC Device Report | |||||||||||||||||||||||||||
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls. 2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall. 3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55. | |||||||||||||||||||||||||||
510(K) Database | 510(K)s with Product Code = MJK and Original Applicant = MEDTRONIC PHYSIO-CONTROL CORP. |