83 results

• Alaris Infusion Pump PC Units Recall Due to Software Errors

  April 23, 2013

  Martha Garcia

  A class 1 recall has been issued for the Alaris Electronic Infusion Pump, which includes two different pump module attachments...

• Baxter Sigma Spectrum Infusion Pump Sold Without FDA Approval

  April 19, 2013

  Martha Garcia

  Federal health investigators indicate that Baxter Healthcare Corporation sold its SIGMA Spectrum Infusion Pump to the public without first getting...

• Symbios GoPump Recall Issued for Disposable Dual Infusion Pump Kits

  March 19, 2013

  Russell Maas

  A recall has been issued for Symbios GoPump dual infusion pump kits due to a faulty flow restrictor bead, which...

• Hospira Medical Device Manufacturing Problems Get FDA Warning

  February 14, 2013

  Irvin Jackson

  Federal regulators have warned Hospira Inc. over the quality of its medical devices, following an inspection of its Lake Forest,...

• Medtronic SynchroMed Pump Problems Linked to Unapproved Drugs

  December 26, 2012

  Irvin Jackson

  Medtronic is warning that its SynchroMed II and SynchroMed EL pumps are failing at a high rate, indicating that the...

• Hospira Symbiq Infusion System Recall: Touchscreen Problems on Pumps

  October 31, 2012

  Russell Maas

  A Class one recalled has been issued for one and two channel Symbiq infusion systems sold by Hospira, due to...

• I-Flow ON-Q Pump Recall Issued for Models With ONDEMAND Bolus Button

  September 4, 2012

  Irvin Jackson

  Several models of the I-Flow On-Q pain pump have been recalled, due to problems with the ONDEMAND bolus button featured...

• Problems at Hospira Infusion Pump Plant Result in FDA Warning

  August 29, 2012

  Irvin Jackson

  Hospira has received an FDA warning letter over conditions at an infusion pump factory in Costa Rica, which the agency...

• Carefusion Alaris Infusion Pump Recall Issued Over Defective Motors

  August 24, 2012

  Staff Writers

  Defective motors have led to the recall of Carefusion Alaris drug infusion pumps, which federal regulators indicate could cause serious...

• Medtronic Manufacturing Violations Puts Patients at Risk: FDA Letter

  August 22, 2012

  Irvin Jackson

  Medtronic’s failure to adequately address reported problems with its SyhcnroMed II infusion pump may have placed patients at risk of...