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Health product recall

Propofol Injection (2015-12-03)

Starting date:
December 3, 2015
Type of communication:
Drug Recall
Subcategory:
Drugs
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-56250

Affected Products

Propofol Injection

Reason

Recalled lot does not meet its vial fill specification.

Depth of distribution

Wholesalers across Canada

Affected products

Propofol Injection (2015-12-03)

DIN, NPN, DIN-HIM
DIN 02437643
Dosage form

Intravenous emulsion

Strength

10 mg/mL, 1% w/v Propofol

Lot or serial number

16IC03

Companies
Recalling Firm
Fresenius Kabi Canada Ltd.
45 Vogell Rd, Ste 200
Richmond Hill
L4B 3P6
Ontario
CANADA
Marketing Authorization Holder
Fresenius Kabi Canada Ltd.
45 Vogell Rd, Ste 200
Richmond Hill
L4B 3P6
Ontario
CANADA

Date modified: