MAGNETOM Aera magnetic resonance system. Indicated for recall
MAGNETOM Aera magnetic resonance system. Indicated for use as a magnetic resonance diagnostic device (MRDD) that produces transverse, sagittal…
Why was MAGNETOM Aera magnetic resonance system. Indicated for recalled?
Siemens discovered a processing error for the MAGNETOM Aera magnetic resonance system that may have resulted in some users not receiving Operator Manuals.
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?
model # 10432914 with serial numbers: 52126 52135 52108 52025 52101
- Product
- MAGNETOM Aera magnetic resonance system. Indicated for use as a magnetic resonance diagnostic device (MRDD) that produces transverse, sagittal…
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 5
- Distribution
- Distributed in the states of MN, CA, CO, TX, and IA.
- Recall date
- June 4, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)