Devices

Device Recall Hospira Phoenix Infusion System with MedNet Software, One Channel Infusion System

Model / Serial
List number 16027-04-83/84 and 87/88, software versions 2.1 and 3.0 only.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed to 59 consignees to all 50 States.
Product Description
Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA
Manufacturer
Hospira Inc
1 Event
- Recall of Device Recall Hospira Phoenix Infusion System with MedNet Software, One Channel Infusion System

Manufacturer

Hospira Inc

Manufacturer Address
Hospira Inc, 755 Jarvis Dr, Morgan Hill CA 95037-2810
Source
USFDA

One device with a similar name

Learn more about the data here

Device Recall Hospira Phoenix Infusion System with MedNet Software, One Channel Infusion System

Model / Serial
List number 16026-04-83/84 and 87/88, software versions 2.1 and 3.0 only.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Product was distributed to 59 consignees to all 50 States.
Product Description
Hospira Phoenix Infusion System with MedNet Software, Symbiq One-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA.
Manufacturer
Hospira Inc

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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