Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens Recalled by Siemens Medical Solutions USA, Inc Due to A particular component may not have been fitted...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Medical Solutions USA, Inc directly.
Affected Products
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Quantity: 1315
Why Was This Recalled?
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Medical Solutions USA, Inc
Siemens Medical Solutions USA, Inc has 613 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report