Kirkland Signature Extra Strength Acetaminophen Tablets 500 mg: Out of Specification
Dernière mise à jour
Summary
Produit
Kirkland Signature Extra Strength Acetaminophen Tablets 500 mg
Problème
Health products - Product quality
Ce qu’il faut faire
Consult your health care professional if you have any health concerns.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
Kirkland Signature Extra Strength Acetaminophen Tablets |
Extra Strength Acetaminophen Tablets 500 mg |
DIN 00605778 |
Tablet |
Acetaminophen 500 mg |
0C26550UZ |
Problème
The dissolution is out of specification in the affected lot.
Ce que vous devriez faire
- 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
Contexte
Depth of recall: Wholesalers
Details
Original published date: 2023-02-13
Type d’avis ou de rappel
Health product recall
Catégorie
Health product - Drugs
Entreprises
Vita Health Products Inc.
150 Beghin Avenue, Winnipeg, MB R2J 3W2
Published by
Health Canada
Audience
General public
Healthcare
Industry
Classe de rappel
Type II
Identification number
RA-72690
History
Registre des changements
2023-02-17: Risk type amended from Type III to Type II.