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Cobas IT Middleware Core Unit (2015-04-01) — recall 53416

Health Canada — Medical Devices · Canada · 2015-04-29 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 53416
Date of alert: 2015-04-29
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: Cobas IT Middleware feature "sample closing" could fail if a "rebuilt sample" message was sent by the host before the "sample closing date" already established by the user. The sample result mismatch may occur, if the customer allows recycling patient's ids and if their system was set to allow "sample rebuild".

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/cobas-it-middleware-core-unit-

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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.

Cobas IT Middleware Core Unit (2015-04-01) — recall 53416

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