Class 2 Device Recall Respironics V60 Ventilator

• Date Initiated by Firm: July 02, 2010
• Date Posted: November 24, 2010
• Recall Status: Terminated on December 01, 2010
• Recall Number: Z-0457-2011
• Recall Event ID: 56147
• 510(K)Number: K082660
• Product Classification: Ventilator, continuous, minimal ventilatory support,facility use - Product Code MNT
• Product: Respironics V60 Ventilator, manufactured by Respironics California Inc. in Carlsbad, CA.
• Code Information: Serial Numbers: SS093803N, 100013661, 100009972, 100010387, 100010388, 100009963, SS093901A, SS093901E, SS0939033, 100009502, 100009676, 100009818, 100009815, 100009909, 100009813, SS093903A, SS093904Z, SS093902N, SS093901W, SS0939027, SS093902J, SS0939046, SS093904N, 100003864, 100009411, SS0938074, 100010234, 100009735, 100009002, 100010019, 100009967, 100010060, 100010101, 100013675, 100009858, 100011301, 100012282, SS0938075, 100009124, 100004133, 100009499, 100011303, 100009563, 100009852, 100009913, SS093800V, SS093802M, SS093802R, SS093805R, 100009917, 100012696, 100004549, SS0938017, 100009665, 100009341, 100009094, 100009765, 100009328, 100012706, 100010204, 100009088, 100010389, 100009667, 100009414, SS093901K, 100013477, 100009087, 100009960, SS093802D, 100009675, 100009004, 100010311, 100010406, SS093801E, 100011744, 100009817, 100009669, 100010052, 100010015, 100010065, 100010386, 100009968, 100009962, 100009941, 100011800, 100009939, 201000202, 100009761, 100009762, 100009679, 100012262, SS093901C, 100010515, 100010231, SS0938026, 100009732, 100012264, 100003665, 100009816, 100009854, 100012769, 100009329, 100009097, 100009856, 100009566, 100009501, 100011308, 100011343, 100010160, SS093806S, 100009424, 100010408, 100009125, 100008995, 100009415, 100009326, 100009674, 100009730, 100010054, 100010512, 100009859, 100009961, 100009971, 100009934, 100009964, 100010016, 100010017, 100010100, 100010383, 100010401, 100010403, 100010510, 100009670, 100010164, 100010057, 100010139, 100009729, 100009731, 100010316, 100009091, 100009671, 100009767, 100009811, 100010018, 100011330, 100011334, 100009734, 100009810, 100009766, 100009938, 100011268, 100011272, 100009943, 100010058, 100010317, 100010384, 100010391, 100010402, 100010511, 100009763, SS0939050, 100009428, 100009423, 100012464, 100010243, 100010518, 100010230, 100009427, 100010315, 100010509, 100010407, 100010504, 100010507, 100010506, 100011339, 100011302, SS093805C, 100009850, 100011329, 100009422, 100003911, 201000493, 100009565, 100009937, 100011269, 100011307, 100009977, 100009936, SS093802P, 100009819, 100009664, 100011263, 100011325, 100010390, 100010519, 100008996, 100010162, 100008799, 100009416, 100009413, 100009005, 100012545, 100009090, 100009092, 100010014, 100009430, 100009412, 100009345, 100009851, 100015074, 100009342, 100009661, 100009337, 100009668, 100009966, 100009247, 100010410, 100010405, 100010409, 100010314, 100010503, 100010505, 100009733, SS093904P, 100011337, 100009673, 100011336, 100011309, 100011338, 100011340, 100009420, 100009672, 100009666, 100009245, 100009419, 100009418, 100009340, 100009332, 100003668, 100008998, 100011306, 100009855, 100008790, 100011341, 100011326, 100011265, 100011335, 100010272, SS0938071, SS0938042, 100014139, 100009662, 100010209, 100010241, 100010240, 100010244, 100010064, 100010270, 100010277, 100010278, 100010309, 100010310, 100009085, 100009678, 100009764, SS093806B, 100009814, 100009677, 100011328, 100011266, 100011270, 100011267, SS093800Y, SS093806W, 100009857, 100010404, SS0938036, 100008797, 100012765, 100012762, 100012654, 100003683, 100009975, 100010313, 100010279, 100010308, 100009264, 100009327, 100009335, 100009812, 100012775, 100010508, 100009970, 100010166, 100010312, 100010513, 100009003, 100009912, 100009916, 100009343, 100010520, 100011271, 100011300, 100010385, 100010382, 100009093, 100012658, 100009246, 100009429, 100009089, 100008796, 100010275, 100012648, 100009330, 100009120, 100010517, 100012267, 100012265, 100011331, 100011342, 100010276, 100009122, 100008795, 100008798, 100009096, 100009338, 100009001, 100009098, 100012652, 100012661, 100012166, 100012690. 100009853, 100009931, 100011264, 100011333, 100011327, 100005394, 100009123, 100009344, 100008997, 100009932, 100009000, 100008999, 100004130, 100009564, 100009086, 100011304, 100010514, 100010274, 100010516, 100010169, 100008437
• FEI Number: 2518422
• Recalling Firm/ Manufacturer: Respironics California Inc; 2271 Cosmos Ct; Carlsbad CA 92011
• For Additional Information Contact: 760-918-7300
• Manufacturer Reason for Recall: Respironics California Inc has received customer complaints of an odor or burning smell coming from the V60 Ventilator, and identified a component on the Power Management PCB that exhibited thermal damage.
• FDA Determined Cause: Device Design
• Action: Phililps Healthcare issued an Urgent Medical Device Field Correction letter dated July 2, 2010 concerning the RespironicsV60 Ventilator issue. Customers will be contacted by US Field Service Technicians and international distributors to schedule and perform inspections and replacement of the affected component. The unit may continue to be used pending completion of the field inspection. Customers may contact Respironics US Customer Service about this action at 1 800 345 6443, option #5, then option #1.
• Quantity in Commerce: 504
• Distribution: Worldwide Distribution: Throughout the US and Puerto Rico,, and to the countries of: Australia, Austria, Belgium, Canada, Denmark, France, Germany, Hong Kong, India, Italy, Kenya, Kuwait, Libya, Malaysia, Oman, Netherlands, Norway, the United Kingdom, Saudi Arabia, and Spain.
• Total Product Life Cycle: 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 = MNT