550 TxT Treatment Table of the Digital Linear Accelerator — Class II medical device recall Z-1645-2014
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2014-05-28, distributed nationwide. Table may lose calibration during patient treatment, which may cause the possibility of mistreatment.
| Recall number | Z-1645-2014 |
|---|---|
| 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 | 2014-05-21 |
| Reported by FDA | 2014-05-28 |
| Terminated | 2014-12-11 |
| Distributed | Nationwide (US) |
| Quantity | 120 |
| Serial numbers | 2765, 3089, 3287, 3413, 3524, 3631, 3695, 3769, 3778, 3793, 3817, 3825, 3835, 3873, 3975, 4059, 4079, 4082, 4091, 5033, 5060, 5087, 5088, 5093, 5095 and 95 more |
Product
550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) To deliver X-ray radiation for therapeutic treatment of cancer.
Reason for recall
Table may lose calibration during patient treatment, which may cause the possibility of mistreatment.
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-1645-2014. 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.