Product Wiki · Recalls · Health Canada — Medical Devices

Roche Diagnostics Assays (2016-10-27) — recall 56337

Health Canada — Medical Devices · Canada · 2016-12-13 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
56337
Date of alert
2016-12-13
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: This recall/product correction is related to a possible sample carry-over for some HIA reagent across Roche systems platforms (Cobas C311/501/502/701/702, Modular P and Cobas Integra 800).
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/roche-diagnostics-assays-2016-

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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