FDA Device recall Z-0515-2013
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
- FDA Device
- Class II
- terminated
- Published 2012-12-19
On 2012-12-19 the FDA classified a Class II recall of MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light by Siemens Medical Solutions Usa, citing A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0515-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-10 |
| Published | 2012-12-19 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Siemens Medical Solutions Usa |
| Distribution | US |
Product
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Reason
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
Identifiers
| code_info | Part numbers 7721165, 4787714, 7559375, 10281150, 10281151, 10281152 and 10281183 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0515-2013%22
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