Siemens Medical Solutions USA, Inc Si emans Evansi, with patient table, Part No: 44 81 586, and without patient table Part No: 44-81-669; Siemens Medical Solutions USA, Concord, CA 94520 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Si emans Evansi, with patient table, Part No: 44 81 586, and without patient table Part No: 44-81-669; Siemens Medical Solutions USA, Concord, CA 94520
Brand
Siemens Medical Solutions USA, Inc
Lot Codes / Batch Numbers
All Serial Numbers (1182 and higher): 1501, 1516, 1213, 1225, 1200, 1518, 1201, 1520, 1246, 1228, 1197, 1202, 1224, 1231, 1191, 1184, and 1506, "MEVASIM", Serial Numbers (1182 and higher): 1204, 1192, 1216, 1502, 1230, 1220, 1209, 1233, 1510, 1241, 1194, 1514, 1523, 1212, 1222, 1252, 2012, 2010-335-217, 1249, 4000296842, S1144, 01069H400, 1503, 1517, 1251, 1238, 1274, 1509, and 1519
Products Sold
All Serial Numbers (1182 and higher): 1501, 1516, 1213, 1225, 1200, 1518, 1201, 1520, 1246, 1228, 1197, 1202, 1224, 1231, 1191, 1184, and 1506, "MEVASIM", Serial Numbers (1182 and higher): 1204, 1192, 1216, 1502, 1230, 1220, 1209, 1233, 1510, 1241, 1194, 1514, 1523, 1212, 1222, 1252, 2012, 2010-335-217, 1249, 4000296842, S1144, 01069H400, 1503, 1517, 1251, 1238, 1274, 1509, and 1519
Siemens Medical Solutions USA, Inc is recalling Si emans Evansi, with patient table, Part No: 44 81 586, and without patient table Part No: 44-81-66 due to Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Loose Mounting Screws -- Cassette holder may become loose and result in the device dislodging and colliding with the patient.
Recommended Action
Per FDA guidance
Customers were sent a Customer Safety Advisory Notice on February 27, 2007, notifying them that the mounting screws on the cassette holders on the SIMVIEW 3000 and NT Simulators, as well as some MEVASIM Simulators, could loosen and can cause damage to the system, or personal injury. The firm requested that they check of tightness on the mounting hardware. A STOP Modification notice was issued on 06/01/2007, to all affected regional service organizations that are responsible for implementing updates due to new information. Updated letters and User instructions will be released in August 2007.
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 noticeDistribution
As reported by FDA
AL, AZ, AR, CA, GA, IL, IN, KS, KY, LA, MA, MI, MN, MO, MT, NE, NJ, NY, NC, ND, OH, OK, PA, SC, SD, TN, TX, VT, VA, DC, PR
Page updated: Jan 10, 2026