Siemens Medical Solutions USA, Inc ANGIOSTAR Plus X-Ray System, Model number 6379718. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ANGIOSTAR Plus X-Ray System, Model number 6379718.
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
Model number 6379718. Serial numbers 1005, 1006, 1011, 1016, 1023, 1033, 1049, 1057, 1059, 1061, 1067, 1069, 1073, 1081, 1082, 1092, 1093, 1095, 1099, 1100, 1101, 1108, 1109, 1113, 1119, 1120, 1121, 1122, 1123, 1127, 1130, 1131, 1134, 1137, 1140, 1144, 1147, 1153, 1155, 1156, 1157, 1159, 1162, 1168, 1169, 1170, 1171, 1172, 1181, 1184, 1186, 1187, 1207, 1210, 1216, 1221, 1223, 1235, 1236, 1241, 1244, 1247, 1248, 1250, 1260, 1261, 1264, 1265, 1267, 1268, 1271, 1272, 1273, 1274, 1275, 1276, 1278, 1284, 1286, 1288, 1290, 1297, 1306, 1308, 1309, 1311, 1313, 1320, 1321, 1335, 1337, 1338, 1345, 1351, 1352, 1354, 1356, 1366, 1367, 1368, 1369, 1371, 1373, 1376, 1378, 1382, 1383, 1385, 1386, 1387, 1388, 1389, 1395, and 9004.
Products Sold
Model number 6379718. Serial numbers 1005, 1006, 1011, 1016, 1023, 1033, 1049, 1057, 1059, 1061, 1067, 1069, 1073, 1081, 1082, 1092, 1093, 1095, 1099, 1100, 1101, 1108, 1109, 1113, 1119, 1120, 1121, 1122, 1123, 1127, 1130, 1131, 1134, 1137, 1140, 1144, 1147, 1153, 1155, 1156, 1157, 1159, 1162, 1168, 1169, 1170, 1171, 1172, 1181, 1184, 1186, 1187, 1207, 1210, 1216, 1221, 1223, 1235, 1236, 1241, 1244, 1247, 1248, 1250, 1260, 1261, 1264, 1265, 1267, 1268, 1271, 1272, 1273, 1274, 1275, 1276, 1278, 1284, 1286, 1288, 1290, 1297, 1306, 1308, 1309, 1311, 1313, 1320, 1321, 1335, 1337, 1338, 1345, 1351, 1352, 1354, 1356, 1366, 1367, 1368, 1369, 1371, 1373, 1376, 1378, 1382, 1383, 1385, 1386, 1387, 1388, 1389, 1395, and 9004.
Siemens Medical Solutions USA, Inc is recalling ANGIOSTAR Plus X-Ray System, Model number 6379718. due to Unintended movement of the system table and/or C arm.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Unintended movement of the system table and/or C arm.
Recommended Action
Per FDA guidance
Siemens Medical Solutions issued a letter to consignees on 8/11/2008 to inform them of the problem and a workaround should the issue occur prior to software revision.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026