Class II — Siemens Medical Solutions USA, Inc
| Recalling firm | SIEMENS MEDICAL SOLUTIONS USA, INC. |
|---|---|
| Registered facility | View this company's 9 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems. |
| Product | MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light |
| Quantity | 1315 |
| Distribution | Nationwide Distribution |
| Initiated | 2012-10-10 |
| Classified | 2012-12-12 |
| Terminated | 2014-11-06 |
| Recall number | Z-0515-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Siemens Medical Solutions USA, Inc (Z-0515-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/63496/
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