Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera — Class II medical device recall Z-1770-2017
Terminated recall by Siemens Medical Solutions USA, Inc, reported 2017-04-19, distributed in DC, MD. Due to a potential manufacturing error, a rare possibility exists for a sudden drop in table height of the Com
| Recall number | Z-1770-2017 |
|---|---|
| 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 | 2016-10-17 |
| Classified | 2017-04-10 |
| Reported by FDA | 2017-04-19 |
| Terminated | 2017-10-24 |
| Distributed | DC, MD |
| Quantity | 3 systems |
| Serial numbers | 12811002, 12811003, 12811017 |
| Model numbers | 10684336, 10684337 |
Product
Combi Dockable Neurosurgery table for the Siemens MAGNETOM Aera (1.5T) and Skyra (3T) MRI Systems
Reason for recall
Due to a potential manufacturing error, a rare possibility exists for a sudden drop in table height of the Combi Dockable Table Neurosurgery.
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-1770-2017. 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.