Brand Recall Hub

Ranitidine Recalls in Canada

18 recalls found for Ranitidine. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

18 Ranitidine Recalls

Other
2022-03-11

Ranitidine products recalled because of a nitrosamine impurity

Product safety

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Health Products Type I
2021-12-03

Acid Reducer (Ranitidine) Tablet: N-nitrosodimethylamine (NDMA) impurity

Contamination

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Health Products Type I
2021-02-04

PMS-Ranitidine 150mg(2021-02-04)

Product safety

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Health Products Type I
2020-08-28

pms-Ranitidine 150mg (2020-08-28)

Product safety

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Health Products Type I
2020-08-27

Ranitidine Injection USP (2020-08-27)

Product safety

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Other
2020-07-23

Status of ranitidine drugs in Canada

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Health Products Type I
2019-10-29

Sun Pharma Canada Inc. Ranitidine Product Recall (2019-10-29)

Product safety

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Health Products Type I
2019-10-24

Vita Health Products Inc Ranitidine Product Recall (2019-10-24)

Product safety

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Health Products Type I
2019-10-24

Laboratoire Riva Inc. Ranitidine Product Recall (2019-10-24)

Product safety

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Health Products Type I
2019-10-23

Pharmascience Inc. Ranitidine Product Recall (2019-10-23)

Product safety

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Health Products Type I
2019-10-17

Teva Canada Ranitidine Product Recall (2019-10-17)

Product safety

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Health Products Type I
2019-10-17

Sivem Pharmaceuticals ULC Ranitidine Product Recall (2019-10-17)

Product safety

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Health Products Type I
2019-09-24

Sivem Pharmaceuticals ULC Ranitidine Product Recall (2019-09-24)

Product safety

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Health Products Type I
2019-09-24

Apotex Inc Ranitidine Product Recall (2019-09-24)

Product safety

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Health Products Type I
2019-09-24

Pro Doc Limitee Ranitidine Product Recall (2019-09-24)

Product safety

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Health Products Type I
2019-09-24

Sanis Health Inc. Ranitidine Product Recall (2019-09-24)

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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Other
2019-09-13

Health Canada assessing NDMA in ranitidine

Product safety

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