Allerject (2015-06-13)
- Starting date:
- June 13, 2015
- Posting date:
- June 16, 2015
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type I
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-53819
Recalled Products
Allerject
Reason
Potential device defect affecting delivery of drug to patient.
Depth of distribution
Retailers
Affected products
Allerject
DIN, NPN, DIN-HIM
DIN 02382059
Dosage form
Solution
Strength
Epinephrine 0.15 mg / 0.15 mL
Lot or serial number
- 2857505
- 2857508
Companies
- Recalling Firm
-
Sanofi-Aventis Canada Inc.
2905 Place Louis.R-Renaud
Laval
H7V 0A3
Quebec
CANADA
- Marketing Authorization Holder
-
Sanofi-Aventis Canada Inc.
2905 Place Louis.R-Renaud
Laval
H7V 0A3
Quebec
CANADA
