Medicine recalls
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| Canada: Recall: Amlodipine Tablet 5mg |
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Health Canada announced that Pro Doc Ltd. is recalling Amlodipine Tablet 5mg (lot no.: 603419 and 603805) as the affected lots exhibit high variability for dosage uniformity. The depth of distribution of the product is wholesalers and pharmacies in Canada.
Health Canada classified the hazard level of the recall as Type II, i.e. a situation in which the use of, or exposure to, a product may cause temporary adverse health consequences or where the probability of serious adverse health consequences is remote.
Please refer to the following website in Health Canada for details:
http://healthycanadians.gc.ca/recall-alert-rappel-avis/hc-sc/../62952r-eng.php
In Hong Kong, the above product is not a registered pharmaceutical product.
Ends/Tuesday, April 11, 2017
Issued at HKT 15:00
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