Product Wiki · Recalls · Health Canada — Medical Devices

Merge IConnect Enterprise Archive (ICEA) — recall 44361

Health Canada — Medical Devices · Canada · 2016-08-26 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
44361
Date of alert
2016-08-26
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: This recall has been initiated due to an issue in ICEA which could result in unrecoverable loss of data when using tiered storage on ICEA. The issue can arise if a study has purged from tier 1 (i.e. via high water mark) and only resides in tier 2 and then the study is requested to be updated.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/merge-iconnect-enterprise-arch

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.