Hazard Hub

Labelling and packaging Recalls in Canada — Page 2

478 recalls involving labelling and packaging — most are medical devices recalls. Newest first, updated daily from government open data.

Showing 31–60 of 478

Other
2026-05-20

CannaPiece Corp. recalls JAYs - Pink Pennifer 0.4g all-in-one vape due to labelling issue

Labelling and packaging

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Consumer Products
2026-05-15

​​Asung Trading Inc. products​ recalled due to missing mandatory hazard labelling​

Labelling and packaging

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Medical Devices Type II
2026-05-14

directCHECK™ Whole Blood Control

Labelling and packaging

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Medical Devices Type II
2026-05-13

VersaPulse Dual Wavelength and CO2 Laser Systems

Labelling and packaging

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Consumer Products
2026-05-08

QS branded cyanoacrylate adhesives and activator recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type II
2026-05-01

HydroMARK™ Breast Biopsy Site Marker

Labelling and packaging

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Consumer Products
2026-04-29

​​ResinAngel brand epoxy resin products​ recalled due to improper labelling

Labelling and packaging

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Consumer Products
2026-04-14

Nordic Easy Glide liquid glide wax recalled due to inappropriate labelling

Labelling and packaging

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Consumer Products
2026-04-10

TJ Trading Co. Inc. products recalled due to missing mandatory hazard labelling

Labelling and packaging

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Medical Devices Type II
2026-04-02

Edwards EVOQUE Tricuspid Delivery System

Labelling and packaging

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Medical Devices Type II
2026-03-17

Approach® CTO Micro Wire Guide, Blue Rhino® G2-Multi Percutaneous Tracheostomy Introducer Set, Wayne Pneumothorax Set, Cook Spectrum® Central Venous Catheter Sets

Labelling and packaging

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Medical Devices Type II
2026-03-13

Monoject™ 1mL Luer Lock Syringe, Tuberculin Print, Sterile

Labelling and packaging

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Consumer Products
2026-03-13

Clore Beauty Supply products​ recalled due to missing mandatory hazard labelling

Labelling and packaging

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Other
2026-03-11

Nextleaf Labs Ltd. recalls Glacial Gold – Anytime 1:1 Fuzzy Mango due to packaging and labelling issue

Labelling and packaging

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Food Class 3
2026-03-10

ICIM brand Halloumi Cheese recalled due to undeclared sheep milk and goat milk

Labelling and packaging

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Medical Devices Type II
2026-03-05

Olympus MAJ-1443 and MAJ-1444 Valves

Labelling and packaging

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Consumer Products
2026-03-04

Elixir -40 C windshield washer fluid recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type I
2026-02-27

Sterile Contro-Vac Whistle Tip Suction Cath W/2 Gloves & Pop-Up Cup Vinyl

Device compatibility - Labelling and packaging

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Medical Devices Type II
2026-02-20

Celon ProBreath and Celon ProSleep Applicators

Labelling and packaging

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Medical Devices Type II
2026-02-04

ViziShot 2 Flex

Labelling and packaging - Performance

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Medical Devices Type I
2026-02-03

EVIS EXERA III Duodenovideoscope

Labelling and packaging

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Medical Devices Type II
2026-01-23

MOLLI 2 Systems

Labelling and packaging

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Medical Devices Type II
2026-01-21

Ventilator Circuit For Non-Invasive Ventilation

Labelling and packaging

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Consumer Products
2026-01-08

Expanded recall: Various Magic BM products recalled due to missing mandatory hazard labelling

Labelling and packaging

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Medical Devices Type II
2026-01-06

Jumper Medical Fetal Doppler

Labelling and packaging

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Medical Devices Type II
2026-01-06

Cardinal Health™ Chest Drain Units and Accessories

Labelling and packaging

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Consumer Products
2026-01-05

McDade Auto -40 Windshield Washer Solvent recalled due to lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type II
2025-12-23

Edan Patient Monitors

Labelling and packaging

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Medical Devices Type II
2025-12-19

Suture/Laceration Tray by Canadian Hospital Specialties Ltd.

Labelling and packaging

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Other
2025-12-16

Wyld Canna Inc d.b.a Wyld Canna recalls Real Fruit Mixed Berry CBD Gummies due to packaging and labelling issue

Labelling and packaging

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Other Medical Devices Hazards

Performance (1,506)Sterility (179)Device compatibility (91)Unauthorised device (78)Software defect (49)Manufacturing defect (31)Inaccurate test or measurement results (29)Quality (25)Increased risk or new adverse events (23)Revised instructions for use (17)Mechanical defect (9)Lack of efficacy (8)

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