Canadian Food Inspection Agency · October 9, 2026
- Affected product
- Kara Food brand Poulet Tandoori recalled undeclared mustard
- Category
- Food recalls
- Hazard
- Kara Food brand "Poulet Tandoori" recalled due to undeclared mustard.
Check affected Kara Food brand Poulet Tandoori recalled undeclared mustard identifiers →Government of Canada Consumer Product Safety · October 9, 2026
- Affected product
- S1 Dry Flush Sealing Toilet and S1 Adapter Kit recalled fire hazard
- Category
- Consumer product recalls
- Hazard
- Brand(s) S1 Last updated 2026-10-09 Summary Product S1 Dry Flush Sealing Toilet and S1 Adapter Kit Issue Consumer products - Fire hazard What to do Immediately stop using the recalled product and
Check affected S1 Dry Flush Sealing Toilet and S1 Adapter Kit recalled fire hazard identifiers →Canadian Food Inspection Agency · October 9, 2026
- Affected product
- Redpath brand Medium Sugar recalled pieces of metal
- Category
- Food recalls
- Hazard
- Redpath brand Medium Sugar recalled due to pieces of metal.
Check affected Redpath brand Medium Sugar recalled pieces of metal identifiers →Canadian Food Inspection Agency · October 9, 2026
- Affected product
- Kevin’s Natural Foods brand Turkey Gravy recalled undeclared mustard
- Category
- Food recalls
- Hazard
- The affected product is being recalled from the marketplace because it contains mustard which is not declared on the label.
Check affected Kevin’s Natural Foods brand Turkey Gravy recalled undeclared mustard identifiers →Health Canada · October 8, 2026
- Affected product
- FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version
- Category
- Medical device recalls
- Hazard
- Under specific conditions following a deep battery discharge, error 29515 may occur during startup of a FreeO2 HW 2.3 device using software package 1.4.2 and prevent its use. The update to software package 1.4.3 corrects this issue and restores the expected…
Check affected FreeO2 Automated Oxygen Therapy Device Adult & Pediatric - Version identifiers →Government of Canada Consumer Product Safety · October 8, 2026
- Affected product
- Studio Six Headphone Amplifier recalled electric shock hazard
- Category
- Consumer product recalls
- Hazard
- Brand(s) Studio Six Last updated 2026-10-08 Summary Product Studio Six Headphone Amplifier Issue Consumer products - Electrical hazard What to do Immediately stop using the recalled product and
Check affected Studio Six Headphone Amplifier recalled electric shock hazard identifiers →Health Canada · October 8, 2026
- Affected product
- TruSystem 7000 and TruSystem 7500 Surgical Tables
- Category
- Medical device recalls
- Hazard
- Baxter Corporation is issuing a voluntary correction for certain TruSystem 7000 and TruSystem 7500 surgical tables due to a reported issue with the main lift mechanism. The issue has been associated with unexpected wear of the main lift assembly, also known as…
Check affected TruSystem 7000 and TruSystem 7500 Surgical Tables identifiers →Health Canada · October 8, 2026
- Affected product
- Avantage Inserter Handles and Grippers
- Category
- Product recall
- Hazard
- It was identified while using the Avantage inserter handles and grippers during the implantation of the acetabular shell, that the acetabular shell may not consistently disengage from the gripper when the trigger is unlocked. As a result, the inserter handle…
Check affected Avantage Inserter Handles and Grippers identifiers →Government of Canada Consumer Product Safety · October 8, 2026
- Affected product
- GIANT SureLock Bicycle Locks with LED Key recalled ingestion hazard
- Category
- Consumer product recalls
- Hazard
- Brand(s) GIANT Last updated 2026-10-08 Summary Product GIANT SureLock Bicycle Locks with LED Key Issue Consumer products - Ingestion hazard What to do Immediately stop using the recalled product and return it to a GIANT retailer for a partial refund. Previous…
Check affected GIANT SureLock Bicycle Locks with LED Key recalled ingestion hazard identifiers →Health Canada · October 8, 2026
- Affected product
- Cardinal Health Presource Kits
- Category
- Medical device recalls
- Hazard
- Cardinal Health Presource® has identified various kits that may contain a component impacted by the welmed, extension tubing sets component. that advisory was issued to inform customers of a product condition identified in certain lots and to provide…
Check affected Cardinal Health Presource Kits identifiers →Canadian Food Inspection Agency · October 8, 2026
- Affected product
- Nora's brand Mint Chip Non-Dairy Frozen Dessert recalled undeclared
- Category
- Food recalls
- Hazard
- The affected product is being recalled from the marketplace because it contains peanut which is not declared on the label.
Check affected Nora's brand Mint Chip Non-Dairy Frozen Dessert recalled undeclared identifiers →Government of Canada Consumer Product Safety · October 8, 2026
- Affected product
- DR Power Pilot and Premier Trimmers recalled fire and burn
- Category
- Consumer product recalls
- Hazard
- Brand(s) DR Power Last updated 2026-10-08 Summary Product DR Power Pilot and Premier Trimmers Issue Consumer products - Fire hazard Consumer products - Burn hazard What to do Immediately stop using the recalled product and
Check affected DR Power Pilot and Premier Trimmers recalled fire and burn identifiers →Canadian Food Inspection Agency · October 8, 2026
- Affected product
- President’s Choice brand English-Style Gingersnap Cookies recalled
- Category
- Food recalls
- Hazard
- President’s Choice brand English-Style Gingersnap Cookies recalled due to metal wire.
Check affected President’s Choice brand English-Style Gingersnap Cookies recalled identifiers →Government of Canada Consumer Product Safety · October 7, 2026
- Affected product
- Esjay Toddler Busy Board Montessori Toys recalled choking hazard
- Category
- Baby product recalls, Consumer product recalls
- Hazard
- Brand(s) Esjay Last updated 2026-10-07 Summary Product Esjay Toddler Busy Board Montessori Toys (blue with dinosaurs) Issue Consumer products - Choking hazard What to do Immediately stop using the recalled products and
Check affected Esjay Toddler Busy Board Montessori Toys recalled choking hazard identifiers →Canadian Food Inspection Agency · October 7, 2026
- Affected product
- Bahía Paloma brand Grapefruit Paloma Agave Spirit Cocktail and Easy
- Category
- Food recalls
- Hazard
- Bahía Paloma brand Grapefruit Paloma Agave Spirit Cocktail and Easy Vodka brand Raspberry Lemonade Alcoholic Beverage recalled due to spoilage.
Check affected Bahía Paloma brand Grapefruit Paloma Agave Spirit Cocktail and Easy identifiers →Health Canada · October 7, 2026
- Affected product
- GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive
- Category
- Product recall
- Hazard
- Gore has identified through quality control testing that some VIABAHN® devices were processed using equipment that was functioning outside of the validated range. This could potentially result in an incorrect bonding location of the distal tip onto the…
Check affected GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive identifiers →Canadian Food Inspection Agency · October 7, 2026
- Affected product
- Ashoka brand Masala Paneer Kathi Roll recalled undeclared sesame
- Category
- Food recalls
- Hazard
- Ashoka brand Masala Paneer Kathi Roll recalled due to undeclared sesame.
Check affected Ashoka brand Masala Paneer Kathi Roll recalled undeclared sesame identifiers →Health Canada · October 7, 2026
- Affected product
- Perma-Sharp Sutures
- Category
- Product recall
- Hazard
- Perma-sharp sutures are manufactured for Hu-Friedy by 2 manufacturers. 1. Surgical Specialties Corporation has cleared for the U.S. market & 2. Camark SA are authorized for the European Union, United Kingdom, Switzerland, & Israel. Products have same…
Check affected Perma-Sharp Sutures identifiers →Health Canada · October 6, 2026
- Affected product
- Cardinal Health General Procedure Tray
- Category
- Medical device recalls
- Hazard
- Cardinal Health was recently informed of a medical device recall from Becton Dickinson concerning the BD Alaris™ Pump Infusion sets used with BD Alaris™ pump module model 8100 referenced.Tthe recall is being issued due to BD requesting the discontinuation of…
Check affected Cardinal Health General Procedure Tray identifiers →Canadian Food Inspection Agency · October 6, 2026
- Affected product
- SeaQuest brand Shrimp Ring with Mild Cocktail Sauce and President's
- Category
- Food recalls
- Hazard
- SeaQuest brand Shrimp Ring with Mild Cocktail Sauce and President's Choice brand Black Tiger Shrimp with Mild Cocktail Sauce recalled due to undeclared mustard.
Check affected SeaQuest brand Shrimp Ring with Mild Cocktail Sauce and President's identifiers →Health Canada · October 6, 2026
- Affected product
- PMS-Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected PMS-Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Health Canada · October 6, 2026
- Affected product
- Fluoroplastic Vent Tube
- Category
- Product recall
- Hazard
- Vent tube devices across lot 0231048280 were identified to have been released to customers without undergoing sterilization. the issue is currently understood to originate from manufacturing (load preparation) and represents a fault condition: the product does…
Check affected Fluoroplastic Vent Tube identifiers →Health Canada · October 6, 2026
- Affected product
- Medline Bariatric Rollator
- Category
- Medical device recalls
- Hazard
- Specific lots of Medline BariatricRollator (SKU: MDS86800XWS), are being recalled due to the front fork stem bolt/wheel assembly disconnecting from the rollator frame tubing. The immediate consequences could include falls resulting in head trauma, bone…
Check affected Medline Bariatric Rollator identifiers →Health Canada · October 6, 2026
- Affected product
- Embletta MPR PG
- Category
- Medical device recalls
- Hazard
- of incorrect patient information being associated with a study, loss of diagnostic data, delays in diagnosis, or the need to repeat patient testing. Additional information Details Original
Check affected Embletta MPR PG identifiers →Health Canada · October 6, 2026
- Affected product
- Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Health Canada · October 6, 2026
- Affected product
- FreeO2 Automated Oxygen Therapy Device Adult & Pediatric
- Category
- Product recall
- Hazard
- A battery reading error may occur when certain Freeo2 HW 1.2 devices are restarted following an upgrade from software version 1.2.X to 1.4.X. The error is immediately detectable, prevents the device from being returned to service and requires installation of a…
Check affected FreeO2 Automated Oxygen Therapy Device Adult & Pediatric identifiers →Health Canada · October 6, 2026
- Affected product
- FreeO2 Automated Oxygen Therapy Device Adult & Pediatric
- Category
- Medical device recalls
- Hazard
- A battery reading error may occur when certain Freeo2 HW 1.2 devices are restarted following an upgrade from software version 1.2.X to 1.4.X. The error is immediately detectable, prevents the device from being returned to service and requires installation of a…
Check affected FreeO2 Automated Oxygen Therapy Device Adult & Pediatric identifiers →Transport Canada · October 6, 2026
- Affected product
- FIAT CHRYSLER AUTOMOBILES issued a on the 2500 model
- Category
- Vehicle recalls
- Hazard
- with the steering column control module could cause the electronic stability control (ESC) system not to work. Note: This recall is an expansion of Transport Canada recall no. 2026-192. This problem would cause the electronic stability control (ESC) warning…
Check affected FIAT CHRYSLER AUTOMOBILES issued a on the 2500 model identifiers →Health Canada · October 5, 2026
- Affected product
- PDP-DIPHENHYDRAMINE 25 MG CAPSULE: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-Nitroso-N-Desmethyl Diphenhydramine, is out of specification in the affected lots.
Check affected PDP-DIPHENHYDRAMINE 25 MG CAPSULE: Out-of-specification (Impurity) identifiers →Health Canada · October 5, 2026
- Affected product
- hCG One Step Pregnancy Tests
- Category
- Medical device recalls
- Hazard
- Product may detect low levels of HCG below the stated assay sensitivity which may result in false positive test results in samples from non-pregnant individuals. The package insert is being updated to note that low HCG levels can occur at or after onset of…
Check affected hCG One Step Pregnancy Tests identifiers →Health Canada · October 5, 2026
- Affected product
- Lumify Ultrasound System
- Category
- Product recall
- Hazard
- due to reduced access to wi-fi/cellular. Philips has received reports that these erroneous re-registration events have prevented scanning in pre-hospital environments and delayed care to patients. These pre-hospital events occurred outside of wi-fi or cellular…
Check affected Lumify Ultrasound System identifiers →Health Canada · October 5, 2026
- Affected product
- Carvedilol 25 mg Tablets: Out-of-specification (Impurity)
- Category
- Product recall
- Hazard
- The impurity, N-nitroso-carvedilol, may be out of specification in the affected lots.
Check affected Carvedilol 25 mg Tablets: Out-of-specification (Impurity) identifiers →Canadian Food Inspection Agency · October 3, 2026
- Affected product
- Taeyangcho Gochujang (Hot Pepper Paste) recalled undeclared wheat
- Category
- Food recalls
- Hazard
- The affected products are being recalled from the marketplace because they contain wheat which is not declared on the label.
Check affected Taeyangcho Gochujang (Hot Pepper Paste) recalled undeclared wheat identifiers →Canadian Food Inspection Agency · October 3, 2026
- Affected product
- Smarter Snacks brand Vegan Protein Puff Chili & Lime Flavored
- Category
- Food recalls
- Hazard
- The affected product is being recalled from the marketplace because it contains milk which is not declared on the label.
Check affected Smarter Snacks brand Vegan Protein Puff Chili & Lime Flavored identifiers →Health Canada · October 2, 2026
- Affected product
- Automated Impella® Controllers (AIC)
- Category
- Product recall
- Hazard
- patient populations, may lead to temporary inadequate hemodynamic support or a temporary loss of hemodynamic support. Hospital inventory may continue to be used to ensure continuity of care. Not all units are affected by this issue. Additional information…
Check affected Automated Impella® Controllers (AIC) identifiers →Health Canada · October 2, 2026
- Affected product
- hCG Cassettes
- Category
- Medical device recalls
- Hazard
- Product may detect low levels of HCG below the stated assay sensitivity which may result in false positive test results in samples from non-pregnant individuals. The package insert is being updated to note that low HCG levels can occur at or after onset of…
Check affected hCG Cassettes identifiers →Health Canada · October 2, 2026
- Affected product
- Medline Single Sterile C-Section Drapes W/Incise
- Category
- Product recall
- Hazard
- Medline Industries, LP is issuing a correction notice for specific lot numbers of the Medline single sterile C-section drapes w/incise due to customer reports of C-section drapes being difficult to remove from patients, leaving adhesive residue on the…
Check affected Medline Single Sterile C-Section Drapes W/Incise identifiers →Health Canada · October 1, 2026
- Affected product
- Radiography 7000 M
- Category
- Medical device recalls
- Hazard
- Philips has become aware of a potential safety issue impacting the Radiography 7000 M system (Model 712010) where the drive function may fail immediately after an exposure, causing the system to remain stationary. The issue may occur with the Radiography 7000…
Check affected Radiography 7000 M identifiers →Health Canada · October 1, 2026
- Affected product
- Ethicon Nylon Suture
- Category
- Product recall
- Hazard
- Ethicon determined that some ETHILON™ Nylon Suture from the lot subject to this recall (removal) have needles that are distorted/twisted in the primary packaging. Up to 17% of the impacted lot may have the needle defect.
Check affected Ethicon Nylon Suture identifiers →Health Canada · October 1, 2026
- Affected product
- Direxion and Direxion HI-FLO Microcatheters
- Category
- Medical device recalls
- Hazard
- Boston scientific is initiating the removal of specific lots of Direxion and Direxion HI-FLO Microcatheters due to a manufacturing issue that may cause difficulty withdrawing the device from the carrier hoop and difficulty advancing or withdrawing the device…
Check affected Direxion and Direxion HI-FLO Microcatheters identifiers →
