Product Wiki · Recalls · Health Canada — Medical Devices

Spectrum Infusion Pump with Master Drug Library (2013-09-24) — recall 50112

Health Canada — Medical Devices · Canada · 2013-10-31 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
50112
Date of alert
2013-10-31
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Baxter Corporation is recalling one (1) Sigma Spectrum Infusion Pump with Master Drug Library that was shipped with a component that does not meet standards for withstanding an electrostatic discharge in excess of 15 kilovolts. Such exposure could cause the pump to stop unexpectedly with no audible alarm or visual display of the alarm status.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/spectrum-infusion-pump-master-

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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