Symbia T and Symbia T2 computer tomography systems — Class II medical device recall Z-0960-2015
Terminated recall by Siemens Medical Solutions USA, Inc., reported 2015-01-21, distributed nationwide. There are confirmed reports of a component coming loose inside the CT enclosure and damaging the system. compo
| Recall number | Z-0960-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc., Hoffman Estates, IL, United States |
| Recall initiated | 2014-03-05 |
| Classified | 2015-01-13 |
| Reported by FDA | 2015-01-21 |
| Terminated | 2016-12-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BD, BE, BG, BR, CA, CH, CL, CN, CO, CZ, DE, EC, EG, ES, FI, FR, GB, HR, HU, IE, IN, IR, IT, JP, KR, MX, NL, NO, NZ, PH, PL, PT, RU, SE, SG, SI, SK, TH, TN, TW |
| Quantity | 295 systems |
| Serial numbers | 1026, 1028, 1029, 1035, 1040, 1044, 1052, 1054, 1055, 1056, 1057, 1058, 1059, 1060, 1061, 1062, 1063, 1064, 1065, 1066, 1067, 1068, 1069, 1070, 1071 and 176 more |
| Model numbers | 10275007, 10275008 |
Product
Symbia T and Symbia T2 computer tomography systems. These systems are used to perform SPECT, CT, and SPECT + CT scans and imaging studies.
Reason for recall
There are confirmed reports of a component coming loose inside the CT enclosure and damaging the system. components.
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-0960-2015. 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.