Hazard Hub

Labelling and packaging Recalls in Canada — Page 10

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

Showing 271–300 of 467

Consumer Products
2023-09-28

Flikrfire personal Firepots recalled due to lack of appropriate labelling and hazard information

Labelling and packaging

View recall details →

Other
2023-09-25

Cannara Biotech Québec Inc. recalls one lot of Nugz Lemon Linx Reefers dried cannabis pre-rolls

Labelling and packaging

View recall details →

Consumer Products
2023-09-25

EPOARTIST Epoxy Resin Kit recalled due to improper packaging and labelling

Labelling and packaging

View recall details →

Other
2023-09-25

Prime Pot Inc. recalls one lot of EastCann Banana Mints dried cannabis

Labelling and packaging

View recall details →

Medical Devices Type II
2023-09-18

Multichem® S Plus vials

Labelling and packaging

View recall details →

Consumer Products
2023-09-15

Various Chemical Guys brand chemical products in pressurized containers recalled due to improper labelling

Labelling and packaging

View recall details →

Consumer Products
2023-09-12

JDiction Epoxy Resin recalled due to improper labelling

Labelling and packaging

View recall details →

Medical Devices Type II
2023-09-11

Stryker Bipolar Forceps and Generator

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-31

Bivona Pediatric Tracheostomy Tube

Labelling and packaging

View recall details →

Consumer Products
2023-08-29

Soja & Co. ambiance spray recalled due to lack of hazard information

Labelling and packaging

View recall details →

Consumer Products
2023-08-28

Daylogic Dry Shampoo Original recalled due to improper labelling

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-25

Medline Sterile Scissors

Labelling and packaging - Sterility

View recall details →

Medical Devices Type II
2023-08-24

Supermax Nitrile Examination Gloves

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-24

GAMMEX® Non-Latex PI Green Surgical Glove

Labelling and packaging - Sterility

View recall details →

Medical Devices Type II
2023-08-17

Liquid Assayed Chemistry Control Premium Plus

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-17

Zimmer M/L Taper Taperfemoral Stem

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-16

Lead Clippers

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-15

Bosworth Copaliner Varnish

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-15

Olympus Pulmonary Endoscopes

Labelling and packaging

View recall details →

Consumer Products
2023-08-14

HOME FRAGRANCE reed diffusers recalled due to lack of hazard information

Labelling and packaging

View recall details →

Consumer Products
2023-08-10

Expanded Recall: Cantu Shea Butter Oil Sheen Deep Conditioning Spray recalled due to improper labelling

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-04

Trigen Titanium Nail System - Trochanteric Antegrade Nails (TAN)

Labelling and packaging

View recall details →

Medical Devices Type II
2023-08-04

O-Arm 1000 Imaging System - Base O-Arm

Labelling and packaging

View recall details →

Medical Devices Type I
2023-08-04

Filter/HME Twinstar Plus

Labelling and packaging

View recall details →

Medical Devices Type II
2023-07-27

0.5 Micron Hydrophobic Disc Filter

Labelling and packaging

View recall details →

Medical Devices Type II
2023-07-20

Skin Prep Non Sting Wipes; Swabs

Labelling and packaging

View recall details →

Medical Devices Type II
2023-07-14

Megadyne Mega Soft Patient Return Electrode

Labelling and packaging

View recall details →

Medical Devices Type II
2023-07-14

Swan-Ganz Double Lumen Monitoring Catheter

Labelling and packaging

View recall details →

Consumer Products
2023-07-13

Cantu Shea Butter Oil Sheen Deep Conditioning Spray recalled due to improper labelling

Labelling and packaging

View recall details →

Consumer Products
2023-07-13

STA-BIL 360 Protection recalled due to Improper Labelling

Labelling and packaging

View recall details →

Other Medical Devices Hazards

Performance (1,434)Sterility (176)Device compatibility (86)Unauthorised device (77)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)

Browse all recalls by hazard, allergen & year →