Hydromorphone hydrochloride injection USP (2018-01-31)
- Starting date:
- January 31, 2018
- Posting date:
- January 31, 2018
- 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-65922
Affected Products
Hydromorphone hydrochloride injection USP
Reason
Product sterility may be compromised in affected lot due to the possibility of cracked vials
Depth of distribution
Hospitals in Canada
Affected products
Hydromorphone hydrochloride injection USP
DIN, NPN, DIN-HIM
DIN 02382636Dosage form
Solution
Strength
10mg/mL
Lot or serial number
67240DD
Companies
- Recalling Firm
-
Pfizer Canada Inc.
17300 Trans-Canada Hwy.
Kirkland
H9J 2M5
Ontario
CANADA
- Marketing Authorization Holder
-
Pfizer Canada Inc.
17300 Trans-Canada Hwy.
Kirkland
H9J 2M5
Ontario
CANADA