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Last updated: 2024
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Displaying 1 - 15 of 43 items.
Zyn Nicotine Pouches: Product sold without market authorization (NPN in Canada)
RecallHealth product recall | 2024-06-12
Taisho Pharmaceutical Pabron Gold A (Granules) unlicensed product:, product is labelled to contain dihydrocodeine phosphate that is listed on Schedule I of the CDSA
RecallHealth product recall | 2024-06-10
PMS-PIRFENIDONE 267 & 801 mg: Data integrity concerns with products bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-07
Important Safety and Efficacy Information on ALBRIOZA (sodium phenylbutyrate and ursodoxicoltaurine) – Market Withdrawal and Continued Restricted Access
AlertHealth professional risk communication | 2024-06-07
Mint-Betahistine 8, 16 & 24mg: Data integrity concerns with product's bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-06
Accel-Ondansetron ODT 4 & 8 mg: Data integrity concerns with product's bioequivalence data that could lead to incorrect dosing.
RecallHealth product recall | 2024-06-06
Importation of USA-authorized Carbamazepine Extended-Release Tablets, USP 200 mg and 400 mg due to the current shortage of Canadian-authorized carbamazepine
AlertHealth professional risk communication | 2024-06-05
Jamp Digoxin tablet: Over-sized tablet
RecallHealth product recall | 2024-06-03
Octaplasma solution: exposed to temperatures outside of the recommended storage conditions
RecallHealth product recall | 2024-06-03
Extra Strength Heartburn Relief; Foreign matter
RecallHealth product recall | 2024-05-29
Probiotic antibiotic support capsule: Out-of-specification (Bacterial content)
RecallHealth product recall | 2024-05-27
Swical-Energy Extra-Strength Liquid: Incorrect expiry date
RecallHealth product recall | 2024-05-27
Tisseel Kit; Out-of-specification (Dissolution)
RecallHealth product recall | 2024-05-23
Sanis Health Duloxetine 60 mg Capsule; Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
RecallHealth product recall | 2024-05-16
Sandoz Fesoterodine Fumarate 8 mg tablet; Out-of-specification (diester impurity)
RecallHealth product recall | 2024-05-16