APO-TRAVOPROST-TIMOP PQ: missing the documented justification for the results obtained.
Brand(s)
Last updated
Summary
Product
APO-TRAVOPROST-TIMOP PQ
Issue
Health products - Product quality
What to do
Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
Affected products
| Brand | Product Name | Market Authorization | Dosage Form | Strength | Lot |
|---|---|---|---|---|---|
| APO-TRAVOPROST-TIMOP PQ | APO-TRAVOPROST-TIMOP PQ | DIN 02415305 | Solution | Travoprost - Timolol (Timolol Maleate) 0.004 % / 0.5% | VH4975 |
Issue
The affected lot is missing the documented justification for the results obtained.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product, 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: Retailers
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs
Companies
Apotex Inc.
150 Signet Drive
Toronto, Ontario
M9L 1T9
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type II
Identification number
RA-81371
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