Hazard Hub

Labelling and packaging Recalls in Canada — Page 11

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

Showing 301–330 of 478

Consumer Products
2023-08-14

HOME FRAGRANCE reed diffusers recalled due to lack of hazard information

Labelling and packaging

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Consumer Products
2023-08-10

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

Labelling and packaging

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Medical Devices Type II
2023-08-04

Trigen Titanium Nail System - Trochanteric Antegrade Nails (TAN)

Labelling and packaging

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Medical Devices Type II
2023-08-04

O-Arm 1000 Imaging System - Base O-Arm

Labelling and packaging

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Medical Devices Type I
2023-08-04

Filter/HME Twinstar Plus

Labelling and packaging

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Medical Devices Type II
2023-07-27

0.5 Micron Hydrophobic Disc Filter

Labelling and packaging

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Medical Devices Type II
2023-07-20

Skin Prep Non Sting Wipes; Swabs

Labelling and packaging

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Medical Devices Type II
2023-07-14

Megadyne Mega Soft Patient Return Electrode

Labelling and packaging

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Medical Devices Type II
2023-07-14

Swan-Ganz Double Lumen Monitoring Catheter

Labelling and packaging

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Consumer Products
2023-07-13

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

Labelling and packaging

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Consumer Products
2023-07-13

STA-BIL 360 Protection recalled due to Improper Labelling

Labelling and packaging

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Consumer Products
2023-07-13

SACHAJUAN Hairspray Light and Flexible recalled due to improper labelling

Labelling and packaging

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Medical Devices Type II
2023-07-13

Olympus HF-Resection Electrode

Labelling and packaging

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Medical Devices Type II
2023-07-13

Tearaway Introducer Sets

Labelling and packaging

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Consumer Products
2023-07-12

Royal Purple Royal Flush Cooling System Flush & Cleaner and POR 15 Top Coat Direct to Metal Rust Preventative Paint recalled due to Improper Labelling

Labelling and packaging

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Consumer Products
2023-07-11

Expanded recall: NicPro brand Epoxy Resin Kits recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Consumer Products
2023-07-11

TJX Canada recalls all Vila Hermanos and Fragrance Works ANTIGA 1860 brand reed diffusers due to lack of hazard information

Labelling and packaging

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Consumer Products
2023-07-11

Instantbond Activator recalled due to improper labelling

Labelling and packaging

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Medical Devices Type II
2023-07-04

Olympus Tracheal Intubation Scopes

Device compatibility - Labelling and packaging

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Consumer Products
2023-06-28

Expanded Recall: Elmer’s® Spray Adhesive & Elmer’s® Craftbond Multi-Purpose Spray Adhesive recalled due to improper labelling

Labelling and packaging

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Consumer Products
2023-06-26

STA-BIL Fuel Stabilizer recalled due to Improper Labelling

Labelling and packaging

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Medical Devices Type II
2023-06-21

Aequalis® Flex Revive® Assembly Screw

Labelling and packaging

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Food Class 3
2023-06-20

Black Diamond brand Lactose Free Marble Cheddar Cheese Natural Cheese Slices recalled due to undeclared lactose

Labelling and packaging

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Medical Devices Type II
2023-06-16

Medline Abdominal Aortic Aneurysm Pack

Labelling and packaging

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Consumer Products
2023-06-15

10X Quick Dry Tinted Lace Spray recalled due to improper labelling

Labelling and packaging

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Medical Devices Type II
2023-06-14

Pilling® Handheld Retractors

Labelling and packaging

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Other
2023-06-12

Aaron’s BCBUD Inc. recalls one lot of Lindsay OG dried cannabis and one lot of Island MKU dried cannabis

Labelling and packaging

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Consumer Products
2023-06-06

NicPro brand Epoxy Resin Kits recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type II
2023-06-01

Ogival Interbody Cage, PEEK

Labelling and packaging

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Consumer Products
2023-05-29

East Coast Resin Epoxy Hardeners recalled due to improper labelling

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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