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Allerject 0.15 mg / 0.15 mL (2015-10-28)
- Starting date:
- October 28, 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-55688
Affected Products
Allerject 0.15 mg / 0.15 mL
Reason
Potential device defect affecting delivery of drug to patient.
Depth of distribution
Wholesalers/distributors, pharmacies, hospitals and health care professionals across Canada.
Affected products
Allerject 0.15 mg / 0.15 mL
DIN, NPN, DIN-HIM
DIN 02382059
Dosage form
Sterile auto-injector
Strength
Epinephrine 0.15 mg / 0.15 mL
Lot or serial number
3060865
2974282
2883603
2857508
2692155
2654767
2546918
2506422
2081284
2081285
3060862
2974283
2883600
2857505
2692158
2654764
2546909
2506413
2144101
2081287
2113805
Companies
- Recalling Firm
-
Sanofi Aventis (Canada) Inc.
2905 Louis R. Renaud Place
Laval
H7V 0A3
Quebec
CANADA
- Marketing Authorization Holder
-
Sanofi Aventis (Canada) Inc.
2905 Louis R. Renaud Place
Laval
H7V 0A3
Quebec
CANADA