Z-0134-2009

ANGIOSTAR Plus X-Ray System, Model number 6379718

Name: Z-0134-2009 ANGIOSTAR Plus X-Ray System, Model number 6379718
Creator: Siemens Medical Solutions USA, Inc
Published: 2008-08-11
License: https://open.fda.gov/license/

Siemens Medical Solutions USA, Inc. / initiated 2008-08-11 / Terminated / root cause: software

FDA source

Siemens Medical Solutions USA, Inc began a recall of ANGIOSTAR Plus X-Ray System, Model number 6379718 on 2008-08-11. The reason FDA records is "Unintended movement of the system table and/or C arm". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as software.

Recall record

Recall number: Z-0134-2009
Status: Terminated
Initiated: 2008-08-11
Posted: 2008-11-04
Terminated: 2012-12-21
Recalling firm: Siemens Medical Solutions USA, Inc.
Product: ANGIOSTAR Plus X-Ray System, Model number 6379718.
Product code: IZI System, X-Ray, Angiographic
Reason for recall: Unintended movement of the system table and/or C arm.
Root cause tag: software
FDA root cause: Software design
Action: 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.
Quantity in commerce: 114 units
Distribution: Nationwide.
Product codes and lots: 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.

Product code IZI

K884912Class IIAngiostarSiemens Medical Solutions USA, Inc. / cleared 1989-02-16

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)