SOMATOM go — Class II medical device recall Z-1939-2018
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2018-06-06, distributed nationwide. There is a potential for a software issue that may cause the need for necessary patient rescans.
| Recall number | Z-1939-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2018-04-20 |
| Classified | 2018-05-25 |
| Reported by FDA | 2018-06-06 |
| Terminated | 2019-05-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BD, BO, BR, CH, CL, CN, CR, DE, DZ, ES, GB, GR, ID, IN, IT, JP, KE, KR, KW, LT, MA, NP, PH, PK, PL, PT, PY, RO, SG, SK, TH, TR, UA, ZA |
| Quantity | 4 units |
| Reason classes | software |
| 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 and 268 more |
Product
SOMATOM go.Now, Material Number 11061618 There is a potential for a software issue that may cause the need for necessary patient rescans.
Reason for recall
There is a potential for a software issue that may cause the need for necessary patient rescans.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1939-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.