FDA Device recall Z-1940-2018

SOMATOM Go.Up, Material Number 11061628 There is a potential for a software issue that may cause the need for necessary patient rescans

FDA Device
Class II
terminated
Published 2018-06-06

On 2018-06-06 the FDA classified a Class II recall of SOMATOM Go.Up, Material Number 11061628 There is a potential for a software issue that may cause the need for necessary patient rescans by Siemens Medical Solutions Usa, citing there is a potential for a software issue that may cause the need for necessary patient rescans.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1940-2018
Classification	Class II
Status	terminated
Initiated	2018-04-20
Published	2018-06-06
Last updated	2026-09-13 11:54 UTC
Company	Siemens Medical Solutions Usa
Distribution	US

Product

SOMATOM Go.Up, Material Number 11061628 There is a potential for a software issue that may cause the need for necessary patient rescans.

Reason

There is a potential for a software issue that may cause the need for necessary patient rescans.

Identifiers

code_info	Serial Numbers: 108052, 108053, 108054, 108055, 108056, 108057, 108058, 108059, 108060, 108061, 108… Serial Numbers: 108052, 108053, 108054, 108055, 108056, 108057, 108058, 108059, 108060, 108061, 108062, 108063, 108064, 108065, 108066, 108067, 108068, 108069, 108070, 108071, 108072, 108073, 108074, 108075, 108076, 108077, 108078, 108079, 108080, 108081, 108082, 108083, 108084, 108085, 108086, 108087, 108088, 108089, 108090, 108091, 108092, 108093, 108094, 108095, 108096, 108097, 108098, 108099, 108100, 108101, 108102, 108103, 108104, 108105, 108106, 108107, 108108, 108109, 108110, 108111, 108112, 108113, 108114, 108115, 108116, 108117, 108118, 108119, 108120, 108121, 108122, 108123, 108124, 108125, 108126, 108127, 108128, 108129, 108130, 108131, 108132, 108133, 108134, 108135, 108136, 108137, 108138, 108139, 108140, 108141, 108142, 108143, 108145

code_info

Serial Numbers: 108052, 108053, 108054, 108055, 108056, 108057, 108058, 108059, 108060, 108061, 108…

Serial Numbers: 108052, 108053, 108054, 108055, 108056, 108057, 108058, 108059, 108060, 108061, 108062, 108063, 108064, 108065, 108066, 108067, 108068, 108069, 108070, 108071, 108072, 108073, 108074, 108075, 108076, 108077, 108078, 108079, 108080, 108081, 108082, 108083, 108084, 108085, 108086, 108087, 108088, 108089, 108090, 108091, 108092, 108093, 108094, 108095, 108096, 108097, 108098, 108099, 108100, 108101, 108102, 108103, 108104, 108105, 108106, 108107, 108108, 108109, 108110, 108111, 108112, 108113, 108114, 108115, 108116, 108117, 108118, 108119, 108120, 108121, 108122, 108123, 108124, 108125, 108126, 108127, 108128, 108129, 108130, 108131, 108132, 108133, 108134, 108135, 108136, 108137, 108138, 108139, 108140, 108141, 108142, 108143, 108145

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1940-2018%22

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