Brand Recall Hub

Ez Io Recalls in Canada

13 recalls found for Ez Io. Data sourced from Health Canada, CFIA, and Transport Canada. Updated daily.

13 Ez Io Recalls

Food Class 1
2025-12-19

Various inspiredgo brand products recalled due to Listeria monocytogenes

Listeria

View recall details →
Other
2025-11-06

Unauthorized drugs seized from Ezra Healing in Kelowna, BC may pose serious health risks

Unauthorized product

View recall details →
Other
2024-03-27

Ezetrol (ezetimibe) and the Risks of Drug-Induced Liver Injury and Severe Cutaneous Adverse Reactions

Product safety

View recall details →
Food Class 1
2024-01-16

Glorious Goodies brand Cavendish Crunch Freeze Dried Treats recalled due to undeclared egg, milk, and soy

Egg - Milk - Soy

View recall details →
Consumer Products
2022-11-03

Various "Breeze" style shoes by C. & J. Clark Canada Limited recalled due to potential chemical hazard

Chemical hazard

View recall details →
Other
2021-01-08

Delta 9 Bio-Tech Inc. recalls one lot of Oceanic Sea Breeze dried cannabis

Labelling and packaging

View recall details →
Medical Devices Type II
2020-05-29

EZ-IO Needle + Stabilizer Kit & Needle Sets (2019-10-11)

Medical devices

View recall details →
Medical Devices Type III
2020-05-22

Dimension Vista System Enzymatic Creatinine Assay (ECREA) & EXL System Enzymatic Creatinine (EZCR) Assay (2020-05-08)

Medical devices

View recall details →
Medical Devices Type II
2020-01-20

Dimension Vista System-Enzymatic Creatinine (ECREA) Assay and Dimension EXL System-Enzymatic Creatinine (EZCR) Assay (2019-12-24)

Medical devices

View recall details →
Medical Devices Type II
2019-10-25

EZ-IO Needle Set + Stabilizer Kit (2019-10-11)

Medical devices

View recall details →
Medical Devices Type III
2018-11-28

Arrow EZ-IO 45mm Needle Set + Stabilizer Kit (2018-10-31)

Medical devices

View recall details →
Consumer Products
2018-08-17

Seabreeze International Corp. recalls certain Smart ThermafloTM Heaters

Fire hazard

View recall details →
Health Products Type I
2018-04-19

Bortezomib for Injection (2018-04-18)

Product safety

View recall details →