Hazard Hub

Labelling and packaging Recalls in Canada — Page 4

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

Showing 91–120 of 478

Medical Devices Type II
2025-09-16

Hollow Fiber Hemodialyzers

Labelling and packaging

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Consumer Products
2025-09-09

Update: Raid® Outdoor Ant Nest Destroyer 2 and Raid Max® Wasp & Hornet Foam Bug Killer 2 recalled due to cans showing signs of leaking

Labelling and packaging

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Other
2025-09-03

Emblem Cannabis Corporation recalls Divvy Island Rush Infused Pre-Rolls due to labelling issue

Labelling and packaging

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Consumer Products
2025-08-28

Expanded recall: Various DESIGNME hair products recalled due to improper labelling

Labelling and packaging

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Consumer Products
2025-08-21

NIIX Wish Refillable Vaping Pods recalled due to lack of child resistant packaging

Labelling and packaging

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Other
2025-08-14

Terranueva Pharma Corporation recalls one lot of Nueva+ Le Fameux dried cannabis pre-rolls

Labelling and packaging

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Other
2025-08-14

Hybrid Infusions Ltd. recalls one lot of Charlotte’s Web Grape 5 x 0.5g Infused Pre-Rolls cannabis extract

Labelling and packaging

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Consumer Products
2025-07-31

DESIGNME Hold.Me three way hairspray recalled due to missing mandatory hazard labelling

Labelling and packaging

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Consumer Products
2025-07-31

REF Stockholm dry shampoo recalled due to missing mandatory hazard labelling

Labelling and packaging

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Medical Devices Type II
2025-07-30

Constellation® Vision System Total Plus Vitrectomy Pak

Labelling and packaging

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Other
2025-07-10

Twin Rivers Farm Ltd. recalls one lot of Surf Banana Split dried cannabis pre-rolls, one lot of Surf Layer Cake dried cannabis pre-rolls, and one lot of Surf Mac dried cannabis pre-rolls

Labelling and packaging

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Medical Devices Type II
2025-07-10

Needle Holder

Labelling and packaging

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Medical Devices Type II
2025-07-10

Microbore Extension Set

Labelling and packaging

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Medical Devices Type II
2025-07-04

Biofinity® Toric Multifocal and XR Toric

Labelling and packaging - Sterility

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Consumer Products
2025-06-16

Rust-Oleum Varathane One Step Stain & Polyurethane (Dark Walnut) recalled due to improper labelling

Labelling and packaging

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Consumer Products
2025-06-13

göt2b glued Blasting Freeze Spray recalled due to missing mandatory hazard labelling

Flammability hazard - Labelling and packaging

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Medical Devices Type II
2025-06-12

Heyman Follower

Labelling and packaging

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Consumer Products
2025-06-11

DeckWise® Deck & Wood Cleaner recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type II
2025-06-11

BD FACS™ 7-Color Setup Beads

Labelling and packaging

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Other
2025-05-28

Exka Inc. recalls one lot of Terroir – Royal Gorilla cannabis extract

Labelling and packaging

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Medical Devices Type II
2025-05-22

EVIS EXERA III Duodenovideoscope

Labelling and packaging

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Medical Devices Type I
2025-05-20

Broselow Pediatric Emergency Rainbow Tape

Labelling and packaging

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Medical Devices Type II
2025-05-15

Umbilical Vessel Catheters

Labelling and packaging

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Medical Devices Type II
2025-05-14

OBM - Digital Acquisition Box

Labelling and packaging

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Consumer Products
2025-05-13

DeckWise® Deck & Wood Brightener (16oz) recalled due to improper labelling and lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type I
2025-05-09

EntraFlo Nutrition Delivery System Enteral Feeding Pump

Labelling and packaging

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Medical Devices Type II
2025-05-07

Beckman Coulter Au Immunochemistry System - Apolipoprotein B

Labelling and packaging

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Consumer Products
2025-05-05

Various ProXpédition hunting products recalled due to lack of labelling information

Labelling and packaging

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Consumer Products
2025-04-24

Crystal E-Liquid recalled due to lack of child-resistant packaging

Labelling and packaging

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Medical Devices Type II
2025-04-23

WB Anatomic Healing Abutment XC

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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