FDA Medical Device Recalls (openFDA)
Philips Medical Systems: Gyroscan ACS-NT with software versions R6x, R7x, R8x
- Recall number
- Z-1227-03
- Recalling firm
- Philips Medical Systems
- Product
- Gyroscan ACS-NT with software versions R6x, R7x, R8x
- Status
- Terminated
- Initiated
- 2002-11-21
- Posted
- 2003-09-12
- Terminated
- 2005-01-13
- Reason
- Patient burns from cables near or in contact with the patient during use
- Root cause
- Other
- Action
- On 11/21/02, the firm provided Field Change Order (FCO) 781 00006 to their field employees. This FCO instructed the field employees to visit the consignees and provide them with the addendums to the Instruction For Use Manual.
- Quantity
- 435 total devices
- Distribution
- The firm distributed units to hospitals and medical centers throughout the U.S.
- Lot, serial or model codes
- 6808, 87145, 86595, 50426, 100214, 101131, 63045, 103171, 41391, 38189, 37996, 85119, 84433, 83876, 102571, 86121, X1577, 44876, 86368, 44793, 87011, 101572, 100916, 82507, 85500, 13606, 86147, 76475, 86235, X1663, 38380, 101111, 37929, X1412, 86280, 37941, 38134, 101608, 25924, 84418, 101138, 6947, 86292, 83044, 63046, 86293, 86406, 102095, 50309, 87355, X1348, 101976, 76919, 17533, 37911, X0038, 26178, 85443, 101946, 13056, 41377, 76320, 59428, 84861, 14134, 76480, 101780, 50430, 50430, 50378, 13275, 85139, 45016, 87183, 86559, 102614, 102616, X1374, 101206, 83041, X1664, X1373, X1730, X1084, X1085, X1270, X1582, X1670, X1352, X1083, X1231, X1272, X1669, X1563, X1741, X0165, X1743, X1280, X1086, X0717, X1271, X0942, X0940, X1740, X1081, 86184, 83303, 101056, 103142, 83631, 38415, 59528, 59357, 83616, 101346, 102018, 76477, 38652, 101313, 38508, 50226, 76848, X1759, 86555, 86082, 14117, 86925, 86020, 13894, 103126, 83080, 101874, 17648, 82506, 86410, 86570, 82610, 38731, 17573, 87365, 62659, 82668, 102889, 41346, 87038, 84887, 103207, 86556, X1043, 87311, 52408, X1593, X1753, 83071, 101423, 100679, 38797, 6841, 47029, 13967, 86248, 13754, 101347, 50390, 102548, 87019, 44994, 87605, 101934, 83325, 41392, 86596, 101425, X1594, 82583, X1353, 83306, 25958, 86335, 86317, 76352, 40904, 10009, 85172, 83395, 103258, 45036, 86597, 37938, 100459, 41441, 13748, 38749, 14128, X1756, 101551, 13058, 87135, X1080, 102110, 38143, 37986, 83946, 82955, 100462, 85436, X0034, 62658, 76807, 76469, 25966, 13932, 102724, 87527, 86408, 101188, 38111, 44833, 41362, 41345, 38966, 26219, 26074, 82627, 86411, 85688, 85686, 82626, 87604, 50336, 86019, 87309, 13020, 84860, 38984, X1668, X1602, 13334, 13338, 13948, 102004, 76847, 102003, 6840, 87188, 26149, 13947, 80335, 83802, 10367, 10409, 38345, 85684, 50412, 50411, 100463, 86409, 83804, 38257, 86056, 87033, 45071, X1163, 101162, 102194, 87161, 87146, 84899, 59707, 13413, 85141, 10432, 13977, 58023, 103064, 87018, 86558, 86236, X1693, 102137, 86148, 103143, 84820, 38441, 87062, X0054, 102718, 26150, 103116, 100460, X1757, 82580, 100469, 38661, 86334, 101429, 76321, 101584, 103351, 41250, 85157, 44813, 86560, 82678, 85685, 14065, X1281, 82547, X1595, 41459, 85442, X1662, 41440, X1710, 38650, 101431, 86281, 101432, 83940, 86381, X0084, X1739, 47189, 87053, 38438, 86413, 100323, 10396, 76359, 76358, 17481, 17585, 17483, 17482, 82534, 100461, 86968, 83396, 10353, 86250, 86918, 100478, 83615, 101560, 41064, 13729, 101084, 47043, 17394, 13976, 14144, 84700, 87607, X1216, X1215, 13730, 13864, 100826, 50407, X1648, 17683, 13057, 13966, 87147, 82546, 38651, 86407, 59427, 84478, 84484, 87148, 59384, 59475, 103135, 62953, 86313, 59338, 83394, 59712, 86151, 86083, 62832, 83708, 87310, 26133, 82619, 87168, 87526, 87067, 83051, 101348, X1635, 103041, 102671, 102561, 83916, 38317, 103101, X0162, 84477, 26119, 100785, X1179, X1523, 86080, 85433, 38303, 38304, 86316, 44810, 40975, 83941, 45063, 50432, 101412, 87036, 102907, 45006, 102157, 101165, 101878, 85158, 47058, 41342, 13965, 73974, 86379, 41147, 84859, 102617, 101408, 83995, 83301, 38420, X1649, 86404
- 510(k) numbers
- ["K932645"]
- PMA numbers
- not on file
- Product code
- LNH
- Firm FEI
- 1000524572
- Firm city
- Bothell
- Firm state
- WA
- 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