FDA Recall Terminated

SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product Usage: Sigma Spectrum Volumetric Infusion Pumps with Master Drug Library are intended to be used for the controlled administration of intravenous fluids. These fluids may include pharmaceutical drugs, blood, blood products and mixtures of required patient therapy.

Recall: Z-1484-2014 · Initiated February 7, 2014

Recall

Recall Number
Z-1484-2014
Event Number
67523
Firm
Baxter Healthcare Corp.
FEI Number
1417572
Product Code
FRN
Status
Terminated
Root Cause
Software design
Initiated
February 7, 2014
Posted
April 25, 2014
Terminated
May 25, 2017
Address
1 Baxter Pkwy, Deerfield, IL, 60015-4625

Description

SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library Product Usage: Sigma Spectrum Volumetric Infusion Pumps with Master Drug Library are intended to be used for the controlled administration of intravenous fluids. These fluids may include pharmaceutical drugs, blood, blood products and mixtures of required patient therapy.

Reason

Baxter Healthcare Corporation has issued an Urgent Device Correction for the SIGMA SPECTRUM Volumetric Infusion Pump with Master Drug Library due to repeated System Error 322 occurrences.

Action

On February 7, 2014, Baxter Healthcare Corporation distributed Urgent Device Correction notices and Customer Reply Forms to their customers via first-class mail. Affected customers are instructed to contact Baxter Healthcare Corporation at 1-800-356-3454 (choose option 1) Monday through Friday during the hours of 7:00 am to 7:00 pm Eastern Time. Baxter technicians would determine if an adjustment or repair is necessary. Customers are asked to complete the attached Customer Reply Form and return it to Baxter either by faxing to 1-224-270-5457 or e-mailing a scanned copy to [email protected].

Distribution

Worldwide Distribution - USA Nationwide including PR and the country of Canada.

Quantity

277,096 units (revised)