Dextrose 50 mg/mL Injection; Out of Specification
Last updated
Summary
Product
Dextrose 50 mg/mL Injection USP
Issue
Health products - Product quality
What to do
Consult your healthcare provider prior to discontinuing use of the affected product, or for any health concerns.
Audience
Healthcare
Industry
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot number |
---|---|---|---|---|---|
ICU Medical Canada |
Dextrose 50 mg/mL Injection USP |
DIN 00037915 |
Solution |
Dextrose 50 mg / mL |
5781810 |
Issue
The dextrose content is out of specification in the affected lot.
What you should do
- Verify if your product is affected.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional information
Background
Depth of recall: Healthcare establishments
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
ICU Medical Canada Inc.
2600 Alfred-Nobel boul., Suite 100,
Montréal, QC, H4S 0A9 Canada
Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-73732
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