Mevatron M2/Primus Mid-Energy PRIMUS HI
Reported: March 29, 2017 Initiated: February 14, 2017 #Z-1489-2017
Product Description
Mevatron M2/Primus Mid-Energy PRIMUS HI
Reason for Recall
Software update
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 80 systems
- Distribution
- Distributed throughout the United States
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Mevatron M2/Primus Mid-Energy PRIMUS HI. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 80 systems.
Why was this product recalled? ▼
Software update
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 29, 2017. Severity: Moderate. Recall number: Z-1489-2017.
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