Product Wiki · Recalls · Health Canada — Medical Devices

Infusor, Infusor LV, Infusor XLV and Intermate — recall 50440

Health Canada — Medical Devices · Canada · 2013-10-28 · Type II

As described by Health Canada — Medical Devices: Infusor, Infusor LV, Infusor XLV and Intermate - Portable Elastomeric Infusion Systems (2013-09-04)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
50440
Date of alert
2013-10-28
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 initiated important safety information regarding the infusor and intermate portable elastomeric infusion systems. Contact manufacturer for a listing of all product codes affected. Baxter has received complaints for infusion flow rates greater than intended for the referenced portable elastomeric infusion systems. In many cases, the complaint details an over infusion of medication that is the result of uses inconsistent with the instructions for use.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/infusor-infusor-lv-infusor-xlv

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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