Artis Zee Angiographic x-ray systems.
Reported: April 9, 2014 Initiated: February 7, 2014 #Z-1309-2014
Product Description
Artis Zee Angiographic x-ray systems.
Reason for Recall
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
Details
- Recalling Firm
- Siemens Medical Solutions USA, Inc
- Units Affected
- 9
- Distribution
- MN, WI, PA, MI, AL, OH, NC, AR, and NJ.
- Location
- Malvern, PA
Frequently Asked Questions
What product was recalled? ▼
Artis Zee Angiographic x-ray systems.. Recalled by Siemens Medical Solutions USA, Inc. Units affected: 9.
Why was this product recalled? ▼
An inappropriate cable connection was assembled for certain Artis zee systems. which may cause a system failure and possibly lead to a restricted maneuverability of the gantry system.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 9, 2014. Severity: Moderate. Recall number: Z-1309-2014.
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