Product Wiki · Recalls · Health Canada — Medical Devices

Autodelfia Enhancement Solution (2013-10-21) — recall 50181

Health Canada — Medical Devices · Canada · 2013-11-29 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
50181
Date of alert
2013-11-29
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: Four batches of enhancement solution have been identified to be defective. The defect is seen as a high samarium background in Autodelfia assays using Samarium labeled antibody as tracer.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/autodelfia-enhancement-solutio

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