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U.S. Department of Health and Human Services

Class 2 Device Recall

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 Class 2 Device Recallsee related information
Date Initiated by FirmMay 02, 2002
Date PostedSeptember 12, 2003
Recall Status1 Terminated 3 on April 11, 2005
Recall NumberZ-1199-03
Recall Event ID 26579
510(K)NumberK932645 
Product Classification System, Nuclear Magnetic Resonance Imaging - Product Code LNH
ProductGyroscan ACS-NT system
Code Information X1753, X1412, X1595, X1662, 102718, X1757, X1693, X1523, X1740, X1742, 86293, 101206, 86292, X0717, X1602, X1563, X1670, X1648, X1582, 10009, 10353, 86280, 13057, 13056, 4139, 87605, 84700, 86968, 10082, 87604, 86082, 101111, 84899, 87183, 87161, 87146, 86020, 87135, 86121, 86080, 101608, X0083, 87148, 87145, 83306, 83303, 86184, 86147, 84478, 87188, X1759, 86559, 85685, 102095, 83804, 100460, 85433, 83802, 82678, 85119, 83946, 84433, 86019, 83301, 84861, 84860, 87527, 84820, 100786, 84477, 100785, 86083, 101072, 100459, 83325, 84887, 86056, 87147, 83396, 86596, 85684, 62832, 85500, 85688, 86406, 86411, 100916, 85422, 100469, 85686, 86407, 87310, 87309, 86595, 85139, 85172, 63046, 101408, 85141, 86335, 86317, 87033, 85157, 101165, 38317, 86334, 47189,86287, 86288, 101429, 87053
Recalling Firm/
Manufacturer		 Philips Medical Systems
22100 Bothell Everett Highway
Bothell WA 98041
For Additional Information Contact
425-487-7000
Manufacturer Reason
for Recall		Patient burns related to high SAR levels and the combined use of Synergy Body Coil and synergy Flex-M coil
FDA Determined
Cause 2		Other
ActionThe firm issued a Field Change Order to their field personnel instructing them to add new labeling to the User Manual. 05/02/2002 A letter was issued to customers.
Quantity in Commerce112 total for all 3 devices
DistributionThe firm distributed units to hospitals and medical centers nationwide.
Total Product Life CycleTPLC 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) Database510(K)s with Product Code = LNH
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