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FDA Medical Device Recalls (openFDA)

Siemens Medical Solutions USA, Inc: SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.

Recall number
Z-1939-2018
Recalling firm
Siemens Medical Solutions USA, Inc
Product
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.
Status
Terminated
Initiated
2018-04-20
Posted
not on file
Terminated
2019-05-23
Reason
There is a potential for a software issue that may cause the need for necessary patient rescans.
Root cause
Software design
Action
The firm, Siemens Healthineers, sent an "Customer Safety Advisory Notices" letter dated 4/20/2018 beginning on 4/20/18 to its customers. The letter described the product, problem and actions to be taken. The letters provided the following information to customers: How can the operator help to avoid a potential risk of the system? To avoid an unnecessary additional X-ray dose to patients please observe the following instructions: Topic 1: If a reconstruction cannot be started after an examination, please reboot the system and repeat the aborted reconstruction. If the error persists, please contact your local Siemens Healthineers service support team. They can help you to decide whether a rescan is necessary or not. Topic 2: If you change the scan parameters kV or mA (tube HV or current), please wait for at least 12 seconds before you trigger a scan command on the control box. If artifacts are visible in the topogram, please repeat the topogram before starting the volume scan. If you have started a volume scan and detect artifacts in the real time display, please stop the scan immediately to avoid an unnecessary X-ray dose. Topic 3: After an osteoporosis scan has been completed, the Osteo reconstruction needs to be started and completed directly after the scan. Therefore the images should be loaded and checked in CT View&Go before the scan/recon tab card is closed. Please do not close the scan/recon tab card before you have reconstructed and checked all Osteo images. A successful and complete Osteo reconstruction is visualized by full green bars in the column Recon Progress of the Job Status table and by images including the Osteo phantom in the tab card CT View&Go (for details please see Fig. 3 below). An example of a correct Osteo reconstruction is provided in Fig. 2. After checking the successful and complete Osteo reconstruction you may close the scan/recon tab card. What has been done to address these issues? What actions shall be t
Quantity
4 units in US
Distribution
Worldwide Distribution: US (nationwide) including states of: AR, CA, CT, FL, GA, IL, IN, KS, KY, MO, ND, NY, OH, OK, SD, TN, TX, and VA; and countries of: Algeria, Australia, Austria, Bangladesh, Bolivia, Bosnia Herzog., Brazil, Cambodia, Chile, China, Columbia, Costa Rica, Germany, Greece, India, Indonesia, Italy, Japan, Kenya, Kuwait, Lithuania, Mauritius, Morocco, Nepal, Pakistan, Paraguay, Philippines, Poland, Portugal, Republic Korea, Romania, Senegal, Singapore, Slovakia, South Africa, Spain, Switzerland, Thailand, Turkey, Ukraine, and United Kingdom.
Lot, serial or model codes
Serial Numbers: 106041,  106051,  106052,  106053,  106054,  106055,  106056,  106057,  106058,  106059,  106060,  106061,  106062,  106065,  106066,  106067,  106068,  106069,  106070,  106071,  106072,  106073,  106074,  106075,  106077,  106078,  106079,  106080,  106081,  106082,  106083,  106084,  106085,  106086,  106087,  106088,  106089,  106090,  106091,  106092,  106093,  106094,  106095,  106096,  106097,  106098,  106099,  106100,  106101,  106102,  106103,  106104,  106105,  106106,  106107,  106108,  106109,  106110,  106111,  106112,  106113,  106114,  106115,  106116,  106117,  106118,  106119,  106120,  106121,  106122,  106123,  106124,  106125,  106126,  106127,  106128,  106129,  106130,  106131,  106132,  106133,  106134,  106135,  106136,  106137,  106138,  106139,  106140,  106141,  106142,  106143,  106144,  106145,  106146,  106147,  106148,  106149,  106150,  106151,  106152,  106153,  106154,  106155,  106156,  106157,  106158,  106159,  106160,  106161,  106162,  106163,  106164,  106165,  106166,  106167,  106168,  106169,  106170,  106171,  106172,  106173,  106174,  106175,  106176,  106177,  106178,  106179,  106180,  106181,  106182,  106183,  106184,  106185,  106186,  106187,  106188,  106189,  106190,  106191,  106192,  106193,  106194,  106195,  106196,  106197,  106198,  106199,  106200,  106201,  106202,  106203,  106204,  106205,  106206,  106207,  106208,  106209,  106210,  106211,  106212,  106213,  106214,  106215,  106216,  106217,  106218,  106219,  106220,  106221,  106222,  106223,  106224,  106225,  106226,  106227,  106228,  106229,  106230,  106231,  106232,  106233,  106234,  106235,  106236,  106237,  106238,  106239,  106240,  106241,  106242,  106243,  106244,  106245,  106246,  106247,  106248,  106249,  106250,  106251,  106252,  106253,  106254,  106255,  106256,  106257,  106258,  106259,  106260,  106261,  106262,  106263,  106264,  106265,  106266,  106267,  106268,  106269,  106270,  106271,  106272,  106273,  106274,  106275,  106276,  106277,  106278,  106279,  106280,  106281,  106282,  106283,  106284,  106285,  106286,  106287,  106288,  106289,  106290,  106291,  106292,  106293,  106294,  106295,  106296,  106297,  106298,  106299,  106300,  106301,  106302,  106303,  106304,  106305,  106306,  106307,  106308,  106309,  106310,  106311,  106312,  106313,  106314,  106315,  106316,  106317,  106318,  106319,  106320,  106321,  106322,  106323,  106324,  106325,  106326,  106327,  106328,  106329,  106330,  106331,  106332,  106333,  106335,  106336,  106337,  106340,  106341,  106342,  106343,  106345,  106347,  106348,  106349,  106350
510(k) numbers
["K163296"]
PMA numbers
not on file
Product code
JAK
Firm FEI
2240869
Firm city
Malvern
Firm state
PA
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

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