Health product recall

EPINEPHRINE, SODIUM BICARBONATE & DEXTROSE USP INJECTIONS : Possible microbiological contamination.

Brand(s)
Last updated

Summary

Product
EPINEPHRINE INJECTION USP, SODIUM BICARBONATE INJECTION USP & DEXTROSE INJECTION USP
Issue
Health products - Contamination
What to do

Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.

Distribution
National

Affected products

Brand Product Name Market Authorization Dosage Form Strength Lot number
Pfizer EPINEPHRINE INJECTION USP DIN 00710814 Intravenous Solution EPINEPHRINE 1mg / mL LR4585, LN2814, LN2813 & LX1239
Pfizer SODIUM BICARBONATE INJECTION USP DIN 00261998 Intravenous Solution SODIUM BICARBONATE 84 mg / mL LN0968, LP9658, LW7842, LR4597, LN0970, MA4046, MA4048, LY3748, MA8144 & MD0507
Pfizer DEXTROSE INJECTION USP DIN 02468514 Intravenous Solution Dextrose 500 mg / mL LH2756 & LY3589

Issue

 Affected lots may contain the presence of microbiological contamination.

What you should do

  1. Verify if your product is affected.
  2. Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
  3. Contact the recalling firm if you have any questions about the recall.
  4. Report any health product related side effects to Health Canada.
  5. Report any other health product safety complaints to Health Canada.

Additional information

Background

Depth of recall: Retailers

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies

Pfizer Canada ULC
17300 Trans-Canada Highway
Kirkland, QC
H9J 2M5

Published by
Health Canada
Audience
General public
Healthcare
Industry
Distribution
National
Recall class
Type I
Identification number
RA-77775

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