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Kenalog-40 Injection (2014-03-04)
- Starting date:
- March 4, 2014
- Type of communication:
- Drug Recall
- Subcategory:
- Drugs
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Product Safety
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-38689
Recalled products
- Kenalog-40 Injection
Reason
This product may have been exposed to temperatures outside of the recommended storage requirements during their transport from CanadaDrugs.com to Canada Diagnostic Centres in Alberta, Canada. The safety and efficacy of these drugs may be impacted by the temperature excursion.
Note: only the units shipped from CanadaDrugs.com to Canada Diagnostics Centres in Alberta, Canada are affected, not the entire lots.
Depth of distribution
Distributed to Canada Diagnostic Centres in Alberta, Canada.
Note: all other units of these lots of Kenalog 40 mg/mL sold by Bristol-Myers Squibb Canada are not impacted by this recall.
Affected products
A. Kenalog-40 Injection
DIN, NPN, DIN-HIM
DIN 01999869
Dosage form
Suspension
Strength
- Triamcinolone Acetonide, 40 mg/mL
Lot or serial number
- 3J74513
- 3H66288
- 3L72817
- 3G74417
- 3E73787
Companies
- Recalling Firm
-
CanadaDrugs.com LP
10 Terracon Place
Winnipeg
R2J 4G7
Manitoba
CANADA
- Marketing Authorization Holder
-
Bristol-Myers Squibb Canada
2344 Boul. Alfred-Nobel, Suite 300
Montréal (Saint-Laurent)
H4S 0A4
Quebec
CANADA