Health CanadaGeneral Alert
Type I Product Recall of Propofol Injection, 1 g/100 mL and 500 mg/50 mL Due to the Presence of Particulate Matter - Hospira Healthcare Corporation - For Health Professionals
Published: October 30, 2009Recall ID: 25437Category: generalCountry: Canada
Safety AlertHealth Canada
Canada
Type I Product Recall of Propofol Injection, 1 g/100 mL and 500 mg/50 mL Due to the Presence of Particulate Matter - Hospira Healthcare Corporation - For Health Professionals
Recalling Firm: Marketed health products
Product Description & Identification
Type I Product Recall of Propofol Injection, 1 g/100 mL and 500 mg/50 mL Due to the Presence of Particulate Matter - Hospira Healthcare Corporation - For Health Professionals
Additional Source Details
| Field | Value |
|---|---|
| N I D | 25437 |
| U R L | https://recalls-rappels.canada.ca/en/alert-recall/type-product-recall-propofol-injection-1-g100-ml-and-500-mg50-ml-due-presence |
| Title | Type I Product Recall of Propofol Injection, 1 g/100 mL and 500 mg/50 mL Due to the Presence of Particulate Matter - Hospira Healthcare Corporation - For Health Professionals |
| Archived | 1 |
| Category | Drugs |
| Last updated | 2009-10-30 |
| 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 - Type I Product Recall of Propofol Injection, 1 g/100 mL and 500 mg/50 mL Due to the Presence of Particulate Matter - Hospira Healthcare Corporation - For Health Professionals Check if your household is affected: https://therecallfile.com/recalls/type-i-product-recall-of-propofol-injection-1-g-100-ml-and-500-mg-50-m/CANADA-25437
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