Brand Recall Hub

Taro Recalls in Canada

15 recalls found for Taro. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

15 Taro Recalls

Health Products Type II
2026-02-09

TARO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution

Product quality

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Health Products Type I
2025-07-11

Taro-Doxorubicin Liposomal: may contain particulate matter

Product quality

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Health Products Type II
2025-05-22

TARO-GLICLAZIDE MR: may contain the presence of pink coloured stain (identified as Candesartan Cilexetil)

Product safety

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Health Products Type III
2023-12-08

Taro-Dipyridamole/ASA: impurity

Product quality

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Health Products Type II
2022-09-21

Esomeprazole, Candesartan and Pravastatin Tablets: OOS result for Finished Product Assay and/or Blend Uniformity

Product quality

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Health Products Type II
2022-09-21

Venlafaxine: OOS result for Spheroids Dissolution Rate Profile (DRP)

Product quality

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Health Products Type I
2022-08-10

Taro-Zoledronic Acid: The affected lots may contain particulate matter

Product quality

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Other
2022-08-09

Taro-Zoledronic acid injection drug, used for osteoporosis and Page's disease, recalled because it may contain particulate matter

Product quality

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Health Products Type III
2021-09-13

TARO-Bupropion XL (2021-09-13)

Product safety

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Health Products Type II
2020-11-17

Taro Pharmaceuticals Inc. Product Recall (2020-11-17)

Product safety

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Health Products Type III
2020-07-20

Taro Pharmaceuticals Inc. Product Recall (2020-07-20)

Product safety

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Other
2020-03-31

Certain Lots of Taro-Zoledronic acid injection drug, used for osteoporosis and Paget's disease, recalled due to potential presence of particulate matter

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Health Products Type I
2020-03-30

Taro-Zoledronic Acid (2020-03-30)

Product safety

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Health Products Type II
2020-01-29

Taro-Carbamazepine (2020-01-29)

Product safety

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Health Products Type III
2018-09-17

Taro-Tramadol 300mg Tablet (2018-09-17)

Product safety

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