MAGNETOM Spectra magnetic resonance diagnostic devices recall
MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
Why was MAGNETOM Spectra magnetic resonance diagnostic devices recalled?
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
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?
Serial # 72030 72023
- Product
- MAGNETOM Spectra magnetic resonance diagnostic devices Model # 10837643
- Recalling firm
- Siemens Medical Solutions USA, Inc
- Quantity
- 2
- Distribution
- AL AR AZ CA CO CT DC DE FL GA GU IA ID IL IN KS KY LA MA MD ME MI MN MO MT NC NE NH NJ NY OH OK OR PA SC TN TX VA WA WI WV WY
- Recall date
- August 28, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)