Medicine recalls
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| Canada: Sandoz Fesoterodine Fumarate 8 mg tablet; Out-of-specification (diester impurity) |
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Health Canada announces that Sandoz Canada Incorporated is recalling 3 lots of Sandoz Fesoterodine Fumarate 8 mg tablet (extended-release) (lot number: 2205009088, 2205010476 and 2205011235) from retailers because the diester impurity is out of specification in the affected lots.
Please refer to the following website in Health Canada for details:
http://recalls-rappels.canada.ca/en/alert-recall/sandoz-fesoterodine-fumarate-8-mg-tablet-out-specification-diester-impurity
In Hong Kong, the above product is not a registered pharmaceutical product.
Ends/Friday, May 17, 2024
Issued at HKT 16:15
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