Health CanadaGeneral Alert
Archived – Serious Adverse Reactions in Pediatric Patients Treated with ORTHOCLONE OKT*3 (muromonab-CD3) – Notice to Hospitals
Published: May 13, 2004Recall ID: 24536Category: generalCountry: Canada
Safety AlertHealth CanadaCanada
CanadaArchived – Serious Adverse Reactions in Pediatric Patients Treated with ORTHOCLONE OKT*3 (muromonab-CD3) – Notice to Hospitals
Recalling Firm: Marketed health products
Reason for Recall / Hazard
Product safety
Product Description & Identification
Archived – Serious Adverse Reactions in Pediatric Patients Treated with ORTHOCLONE OKT*3 (muromonab-CD3) – Notice to Hospitals
Additional Source Details
| Field | Value |
|---|---|
| N I D | 24536 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/archived-serious-adverse-reactions-pediatric-patients-treated-orthoclone-okt3 |
| Issue | Product safety |
| Title | Archived – Serious Adverse Reactions in Pediatric Patients Treated with ORTHOCLONE OKT*3 (muromonab-CD3) – Notice to Hospitals |
| Archived | 1 |
| Category | Biologic or vaccine |
| Last updated | 2004-05-13 |
| Organization | Marketed health products |
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Overview
- Recalling FirmMarketed health products
Recall Hazard Severity
Official Agency AlertCaution (Class III)
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🚨 SAFETY ALERT: Marketed health products - Archived – Serious Adverse Reactions in Pediatric Patients Treated with ORTHOCLONE OKT*3 (muromonab-CD3) – Notice to Hospitals Check if your household is affected: https://therecallfile.com/recalls/archived-serious-adverse-reactions-in-pediatric-patients-treated-with/CANADA-24536
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