Brand Recall Hub

Authorization Recalls in Canada

34 recalls found for Authorization. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

34 Authorization Recalls

Health Products Type I
2026-04-15

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2026-04-14

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type III
2026-04-02

Aved products recall: No market authorization

Unauthorized product

View recall details →

Health Products Type I
2026-03-19

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2026-03-12

Cream Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2025-12-09

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2025-11-28

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2025-11-10

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Product safety

View recall details →

Health Products Type I
2025-11-05

Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)

Unauthorized product

View recall details →

Health Products Type III
2025-09-25

No7 Restore & Renew Face & Neck Multi Action Day Cream SPF 30; No QA authorization

Other

View recall details →

Health Products Type III
2025-09-08

NazalActin Liquid: No market authorization, incorrect NPN, deficiencies in Good Manufacturing Practices

Product quality

View recall details →

Health Products Type III
2025-09-04

Skycare Compounding Laboratories Products recall; No market authorization

Unauthorized product

View recall details →

Health Products Type III
2025-08-22

Ultra Albumin Gold: The addition of the medicinal ingredient albumin is not compliant with its market authorization.

Product safety

View recall details →

Health Products Type III
2025-03-18

All Clean Natural Antibacterial Foaming Hand Wash: No Market Authorization

Unauthorized product

View recall details →

Health Products Type II
2025-03-03

Medline Alcohol Prep Pad: 70% Isopropyl Alcohol: No Market Authorization

Product quality

View recall details →

Health Products Type III
2024-11-13

Actifungi Cream: Affected batches do not comply with the conditions of the product marketing authorization.

Product quality

View recall details →

Health Products Type III
2024-11-04

Dead Down Wind Broad Spectrum SPF 30 Odourless Lip Balm: No Market Authorization

Unauthorized product

View recall details →

Health Products Type II
2024-06-13

XQS Nicotine Pouches 4 & 6 mg: No market authorization

Product safety

View recall details →

Health Products Type II
2024-06-12

Zyn Nicotine Pouches 1.5 & 3mg: No market authorization

Product safety

View recall details →

Health Products Type II
2023-11-03

Pink Cherry Health Products: No market authorization

Unauthorized product

View recall details →

Health Products Type II
2023-08-21

Multi-Peptide Lash Serum: undeclared ingredient and sold without market authorization

Product quality - Unauthorized product

View recall details →

Health Products Type II
2023-05-30

Feather Dream Mint CBD Rapid Spray; No Market Authorization

Unauthorized product

View recall details →

Food Class 3
2023-04-21

Certain Oysters recalled due to improper harvest authorization

Other

View recall details →

Other
2023-01-20

RUZURGI (amifampridine) - Authorization Status

New safety information - Product withdrawal

View recall details →

Health Products Type III
2022-06-30

United Wings Enterprise Inc. recalls COVID-19 Preventive Prescription products sold without market authorization and unauthorized claims.

Unauthorized product

View recall details →

Health Products Type II
2021-12-10

Sesh - Tobacco Free Nicotine Pouch: No Market Authorization

Unauthorized product

View recall details →

Other
2021-10-04

Authorization of Sotrovimab for Injection for Use in Relation to the COVID-19 Pandemic

COVID - Product safety

View recall details →

Other
2021-07-30

Authorization of Casirivimab and Imdevimab with English-only Labels for Use in Relation to the COVID-19 Pandemic

Product safety

View recall details →

Other
2021-03-08

Authorization of Janssen COVID-19 Vaccine with English-only Vial and Carton Labels

COVID - Product safety

View recall details →

Other
2021-03-01

Authorization of AstraZeneca COVID-19 Vaccine with English-only Vial and Carton Labels

COVID - Product safety

View recall details →

Showing 30 of 34 recalls. View all →