Brand Recall Hub

Sandoz Recalls in Canada

14 recalls found for Sandoz. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

14 Sandoz Recalls

Health Products Type II
2025-10-08

Lisinopril HCT 20/25mg: Out-of-specification test results

Product quality

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Health Products Type II
2025-03-21

Sandoz Fesoterodine Fumarate 8 mg tablet; Out of specification (Diester impurity)

Product quality

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Health Products Type II
2024-12-09

SANDOZ FESOTERODINE FUMARATE: The Diester impurity is out of specification in the affected lot(s)

Product safety

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Health Products Type II
2024-05-16

Sandoz Fesoterodine Fumarate 8 mg tablet; Out-of-specification (diester impurity)

Product quality

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Health Products Type II
2021-10-27

Sandoz Orphenadrine: Impurity

Contamination

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Health Products Type I
2021-09-16

Sandoz Canada Losartan/Losartan-HCT Product Recall (2021-09-13)

Product safety

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Health Products Type II
2021-07-19

Sandoz Hydrocortisone 2.5% USP(2021-07-19)

Product safety

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Health Products Type I
2021-05-27

Sandoz-Irbesartan/HCT Product Recall (2021-05-27)

Product safety

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Health Products Type I
2021-05-27

Sandoz-Irbesartan Product Recall (2021-05-27)

Product safety

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Health Products Type I
2021-05-27

Sandoz-Valsartan Product Recall (2021-05-27)

Product safety

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Health Products Type II
2021-01-28

Sandoz Hydrocortisone (2021-01-28)

Product safety

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Health Products Type II
2021-01-12

Sandoz Irbesartan HCT(2021-01-12)

Product safety

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Health Products Type I
2019-09-17

Sandoz Canada Ranitidine Product Recall (2019-09-17)

Product safety

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Health Products Type I
2018-07-09

Sandoz Valsartan Product Recall (2018-07-09)

Product safety

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