Devices

SPECTRUM Pump

Model / Serial
Software Versions 5.02.06, 6.02.06, and 6.02.11; Affected Serial Numbers: 712090, 723687, 723842, 724966, 725820, 735977, 751130, 752124, 755174, 768538, 771990, 774743, 781406, 783736, 784698, 794466, 805797, 808901, 809113, 812462, 815932, 842120, 857926, 858672, 862085, 863721, 865630, 873459, 889597, 890260, 903748, 912619, 920574, 920589, 956346, 957394, 965402, 966684, 976931, 977550, 978361, 983979, 984066, 984129, 984475, 985946, 987538, 993445, 995291, 996014, 996389, 1013037, 1004377, 1014565, 1014962, 967887, 950671, and 938428.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- USA and Canada.
Product Description
SPECTRUM Pump, Model No. 35700BAX. || Intended to be used for the controlled administration of intravenous fluids.
Manufacturer
Baxter Healthcare Corp.
1 Event
- Recall of SPECTRUM Pump

Manufacturer

Baxter Healthcare Corp.

Manufacturer Address
Baxter Healthcare Corp., 25212 W. Illinois Route 120, Round Lake IL 60073-9799
Manufacturer Parent Company (2017)
Baxter International
Source
USFDA

One device with a similar name

Learn more about the data here

Spectrum Pump

Model / Serial
Manufacturer
Baxter Healthcare Corp.

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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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