MAVIG PORTEGRA 2 system operated in conjuction with a recall
MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Why was MAVIG PORTEGRA 2 system operated in conjuction with a recalled?
A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Part numbers 7721165, 4787714, 7559375, 10281150, 10281151, 10281152 and 10281183
- Product
- MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 1315
- Distribution
- Nationwide Distribution
- Recall date
- December 19, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)