MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Reported: December 19, 2012 Initiated: October 10, 2012 #Z-0515-2013
Product Description
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Reason for Recall
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 1315
- Distribution
- Nationwide Distribution
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 1315.
Why was this product recalled? ▼
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on December 19, 2012. Severity: Moderate. Recall number: Z-0515-2013.
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