FDA Medical Device Recalls (openFDA)
Respironics California Inc: Respironics V60 Ventilator, manufactured by Respironics California Inc. in Carlsbad, CA.
- Recall number
- Z-0457-2011
- Recalling firm
- Respironics California Inc
- Product
- Respironics V60 Ventilator, manufactured by Respironics California Inc. in Carlsbad, CA.
- Status
- Terminated
- Initiated
- 2010-07-02
- Posted
- 2010-11-24
- Terminated
- 2010-12-01
- Reason
- 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.
- Root 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
- 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.
- Lot, serial or model codes
- 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
- 510(k) numbers
- ["K082660"]
- PMA numbers
- not on file
- Product code
- MNT
- Firm FEI
- 2518422
- Firm city
- Carlsbad
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28