Baxter Healthcare Corp.: Medical Device Recall in 2014 - (Recall #: Z-2738-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.

Product Classification:

Class II

Date Initiated: September 3, 2014

Date Posted: October 8, 2014

Recall Number: Z-2738-2014

Event ID: 69122

Reason for Recall:

One Service Technician may not have correctly serviced specific Sigma Spectrum Infusion Pumps according to established procedures during the time period of 5/5/2014 through 6/3/2014.

Status: Terminated

Product Quantity: USA: 56 units, Canada: 2 units

Code Information:

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.

Distribution Pattern:

Worldwide Distribution -- USA and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated