Product Wiki · Recalls · Health Canada — Medical Devices

CADD Solis VIP Infusion Pump (2018-06-11) — recall 61083

Health Canada — Medical Devices · Canada · 2018-06-29 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
61083
Date of alert
2018-06-29
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The purpose of this Field Safety Notice (FSN) is to inform you of concerns raised by Health Canada regarding delivery accuracy of the CADD Solis VIP Pump. This FSN clarifies the environmental factors and product configuration that may have an impact on delivery accuracy for the CADD Solis VIP Pump. This notification does not involve a retrieval of devices.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cadd-solis-vip-infusion-pump-2

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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.