Siemens Linear Accelerator — Class II medical device recall Z-1652-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-06-04, distributed nationwide. Siemens Radiation Oncology became aware that customers may be using the Siemens Linear Accelerator in combinat
| Recall number | Z-1652-2014 |
|---|---|
| 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 | 2014-04-01 |
| Classified | 2014-05-23 |
| Reported by FDA | 2014-06-04 |
| Terminated | 2015-03-16 |
| Distributed | Nationwide (US) |
| Quantity | 9 |
| Serial numbers | 1940035, 2113, 2628, 2855, 2962, 3066, 3361, 3873, 4504200, 5833, 5899, 8139789, 9401654 |
Product
Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray radiation for therapeutic treatment of cancer
Reason for recall
Siemens Radiation Oncology became aware that customers may be using the Siemens Linear Accelerator in combination with stereotactic accessories which have not been validated as being compatible with Siemens LINAC models.
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-1652-2014. 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.