MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Reported: August 28, 2019 Initiated: July 9, 2019 #Z-2342-2019
Product Description
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914
Reason for Recall
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 143
- 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
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
MAGNETOM Aera magnetic resonance diagnostic devices Model # 10432914. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 143.
Why was this product recalled? ▼
Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on August 28, 2019. Severity: Moderate. Recall number: Z-2342-2019.
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