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[Recalled] Association of Xigris (Drotrecogin Alfa Activated) with Mortality in Patients with Single Organ Dysfunction and Recent Surgery – Notice to Hospitals — Product safety | Health Canada 2005-02-03
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | Association of Xigris (Drotrecogin Alfa Activated) with Mortality in Patients with Single Organ Dysfunction and Recent Surgery – Notice to Hospitals |
|---|---|
| Category | Biologic or vaccine |
| Issuing authority | HC |
| Reference | 24182 |
| Country of notice | Canada |
| Hazard type | recall |
| Notice date | 03 February 2005 |
Why it was recalled
According to the HC notice, the identified hazard is: Product safety
This safety recall concerns Biologic or vaccine products distributed in Canada and was recorded by HC. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Review the official notice to confirm whether your unit is affected.
Read the full official notice →
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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