FDA Medical Device Recalls (openFDA)
Chattanooga Corp Inc: VECTRA GENISYS, electromechanical therapeutic ultrasound device, Model No. 2759, Chattanooga Group.
- Recall number
- Z-1636-2008
- Recalling firm
- Chattanooga Corp Inc
- Product
- VECTRA GENISYS, electromechanical therapeutic ultrasound device, Model No. 2759, Chattanooga Group.
- Status
- Terminated
- Initiated
- 2008-02-28
- Posted
- 2008-08-06
- Terminated
- 2010-02-19
- Reason
- Device may fail to administer therapy during use.
- Root cause
- Component design/selection
- Action
- Chattanooga Group sent an Urgent Medical Device Recall letter dated 02/29/2008 to consignees to advise them of problem and the recall. The first group of letters was sent to the distributors via certified mail. The letter stated that the devices were failing and the recall was to the User level. The firm is recalling the devices for repair and calibration. The firm followed with a user notification, by US Mail not certified beginning on March 11, 2008.
- Quantity
- 207 devices
- Distribution
- Nationwide Distribution.
- Lot, serial or model codes
- Serial numbers: 1000, 1002, 1003, 1004, 1005, 1007, 1008, 1010, 1011, 1012, 1013, 1014, 1015, 1016, 1017, 1018, 1019, 1021, 1025, 1026, 1028, 1029, 1030, 1031, 1032, 1034, 1035, 1036, 1037, 1039, 1040, 1042, 1043, 1044, 1045, 1046, 1047, 1050, 1051, 1054, 1056, 1058, 1059, 1060, 1061, 1062, 1064, 1066, 1067, 1069, 1071, 1073, 1074, 1075, 1076, 1077, 1078, 1079, 1081, 1082, 1083, 1085, 1086, 1087, 1088, 1089, 1091, 1095, 1096, 1097, 1100, 1102, 1103, 1112, 1114, 1120, 1121, 1122, 1123, 1124, 1125, 1130, 1135, 1137, 1138, 1141, 1142, 1143, 1145, 1146, 1147, 1148, 1149, 1150, 1153, 1157, 1158, 1162, 1163, 1168, 1169, 1171, 1176, 1177, 1178, 1180, 1181, 1186, 1191, 1193, 1194, 1195, 1196, 1197, 1198, 1200, 1201, 1203, 1206, 1207, 1208, 1209, 1210, 1211, 1213, 1215, 1216, 1217, 1220, 1221, 1222, 1225, 1226, 1227, 1228, 1229, 1231, 1232, 1233, 1235, 1236, 1237, 1238, 1239, 1240, 1241, 1247, 1248, 1249, 1254, 1255, 1256, 1259, 1261, 1262, 1266, 1269, 1273, 1275, 1277, 1278, 1279, 1280, 1281, 1282, 1283, 1285, 1286, 1289, 1291, 1293, 1294, 1295, 1296, 1300, 1301, 1302, 1303, 1304, 1305, 1307, 1308, 1309, 1310, 1313, 1314, 1319, 1320, 1329, 1330, 1333, 1339, 1341, 1344, 1346, 1348, 1349, 1351, 1359, 1360, 1361, 1362, 1363, 1364, 1369, 1370, and 1373
- 510(k) numbers
- ["K031116"]
- PMA numbers
- not on file
- Product code
- IMI
- Firm FEI
- 1000342033
- Firm city
- Hixson
- Firm state
- TN
- 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