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Class 2 Device Recall Symphony DR and ELA Rhapsody DR |
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Date Initiated by Firm |
October 25, 2005 |
Date Posted |
December 02, 2005 |
Recall Status1 |
Terminated 3 on January 28, 2007 |
Recall Number |
Z-0266-06 |
Recall Event ID |
34003 |
PMA Number |
P950029S017 |
Product Classification |
Implantable Pacemaker Pulse-Generator - Product Code DXY
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Product |
Symphony DR model 2550 and ELA Rhapsody DR model 2510. A dual chamber rate-responsive pacemaker that uses both minute ventilation and accelerometer sensors. Sterilization with Ethylene Oxide Gas. Sorin Group, ELA medical, 98, rue Maurice Amoux, 92120 Montrouge - France. Made in France. |
Code Information |
Symphony DR 2250 serial numbers: 238WG020, 243WG055, 246WG094, 246WG109, 250WG029, 303WG027, 303WG038, 303WG074, 303WG078, 306WG073, 309WG262, 314WG057, 315WG188 and 320WG220. Rhapsody DR 2510 Serial numbers: 318WJ010, 318WJ060 and 318WJ061 |
Recalling Firm/ Manufacturer |
ela Medical Llc 2950 Xenium Ln N Ste 120 Plymouth MN 55441-2623
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Manufacturer Reason for Recall |
Through post-market surveillance, ELA Medical has observed that a no-output condition could occur in a limited number of Symphony or rhapsody pacemakers. The no-output condition could occur due to metal migration caused by a specific manufacturing process.
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FDA Determined Cause 2 |
Other |
Action |
A Dear Doctor letter, dated 10/25/05, was sent to all affected doctors. The letter describes the failures and mentions that pacemaker depend patients implanted with devices manufactured in the first group could require prophylactic replacement. |
Quantity in Commerce |
17 |
Distribution |
Devices distributed with the US to AZ, CA, FL, IL, LA, MA, ME, MO, MS, SC, |
Total Product Life Cycle |
TPLC Device Report
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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.
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PMA Database |
PMAs with Product Code = DXY and Original Applicant = MicroPort CRM USA Inc.
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