Diclofenac Sodium Micronized: Out of specification in the affected lot.
Last updated
Summary
Product
Diclofenac Sodium Micronized
Issue
Health products - Product quality
What to do
Consult your health care professional if you have any health concerns.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
Diclofenac Sodium Micronized |
Diclofenac Sodium Micronized |
N/A |
Powder |
N/A |
F601-20E29P1O |
Issue
The Loss on Drying is out of specification in the affected lot.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- 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
AX Pharmaceutical Corp.
100 Tesma Way, Unit 8, Concord
ON L4K 0J9
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type III
Identification number
RA-73363
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