Search Results
Found 12,723 results for "product recalls and alerts"
Food & Beverage
FDA Food
FDA FoodKarison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Karison Foods & Snacks, Inc.
FDA FoodClass II
Karison brand PUNJABI PINNI; NET WT. 12 oz.; Ingredients: Wheat Flour, Butter, Sugar, Almonds, Zero Trans Fat, Vegetable Shortening; UPC: 8 97307 00215 4; Distributed By: Karison Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
Feb 18, 2026Karison Foods & Snacks, Inc.
Food & BeverageFDA Food
FDA FoodKarison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Karison Foods & Snacks, Inc.
FDA FoodClass II
Karison brand BESAN LADDOO; NET WT. 12 oz.; Ingredients: Gram Flour, Butter, Sugar, Zero Trans Fat Vegetable Shortening, Almonds, Cardamom; UPC: 8 9730700240 6; Distributed By: Karson Foods & Snacks Inc., 34 Willowdale Ave., Port Washington, NY 11050; Manufactured in a facility that processes Milk, Eggs, Soybean, Tree nuts, Wheat, Peanuts and other Nuts. Product is packaged in clear plastic containers, 12-(12 oz) units/case.
Product contains milk, which is undeclared in the ingredient statement.
Feb 18, 2026Karison Foods & Snacks, Inc.
Medical DeviceFDA Devices
FDA DevicesIQon Spectral CT; Product Code (REF): 728332;
Philips North America Llc
FDA DevicesClass II
IQon Spectral CT; Product Code (REF): 728332;
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Feb 18, 2026Philips North America Llc
PharmaceuticalFDA Drugs
FDA DrugsOxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11
Amerisource Health Services LLC
FDA DrugsClass II
Oxycodone Hydrochloride Tablets, USP (CII), 5 mg, 100-Count (10 x 10) blister cards per carton, Rx Only, The drug product contained in this package is from NDC # 10702-018, KVK-Tech Inc. Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC 68084-354-01; Blister NDC 68084-354-11
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
Feb 18, 2026Amerisource Health Services LLC
Medical DeviceFDA Devices
FDA DevicesBrand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Elekta, Inc.
FDA DevicesClass II
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This may result in a treatment plan that potentially irradiates the incorrect patient location if the error is not detected by users.
Feb 18, 2026Elekta, Inc.
Safety Alert
Health Canada
Health CanadaSunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Consumer product safety
Health CanadaGeneral Alert
Sunshade and alternating blind by Stores d’aujourd’hui Gatineau Inc. recalled due to strangulation and choking hazards
Choking hazard - Strangulation hazard
Feb 18, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaKlask 4 recalled due to ingestion hazard
Consumer product safety
Health CanadaGeneral Alert
Klask 4 recalled due to ingestion hazard
Ingestion hazard
Feb 18, 2026Consumer product safety
Food & BeverageFDA Food
FDA FoodOre-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag (6/5 lb bags), Net Wt. 30 lbs (13.6 kg)/ case. UPC on 30 lbs case label: 1 00 72714 00215 8. Manufactured by McCain Foods USA Inc. McCain distributed this product to foodservice accounts and product was not sold at retail stores.
McCain Foods USA Inc
FDA FoodClass II
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag (6/5 lb bags), Net Wt. 30 lbs (13.6 kg)/ case. UPC on 30 lbs case label: 1 00 72714 00215 8. Manufactured by McCain Foods USA Inc. McCain distributed this product to foodservice accounts and product was not sold at retail stores.
Foreign material (small hard plastic fragments).
Feb 18, 2026McCain Foods USA Inc
Medical DeviceFDA Devices
FDA DevicesSpectral CT; Product Code (REF): 728333;
Philips North America Llc
FDA DevicesClass II
Spectral CT; Product Code (REF): 728333;
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
Feb 18, 2026Philips North America Llc
Food & BeverageFDA Food
FDA FoodKirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
Costco Wholesale Corporation
FDA FoodClass I
Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
Undeclared hazelnut.
Feb 18, 2026Costco Wholesale Corporation
Medical DeviceFDA Devices
FDA DevicesBrand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Elekta, Inc.
FDA DevicesClass II
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11,3, 11.4 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Due to an error when defining a new stereotactic reference that users fail to first change an already defined obsolete reference to a pre-plan reference. This may result in a treatment plan that potentially irradiates the incorrect patient location if the error is not detected by users.
Feb 18, 2026Elekta, Inc.
Safety AlertHealth Canada
Health CanadaHaleine Fraîche oral hygiene product recalled due to a chemical hazard
Consumer product safety
Health CanadaGeneral Alert
Haleine Fraîche oral hygiene product recalled due to a chemical hazard
Chemical hazard
Feb 17, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaPatchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients
Consumer product safety
Health CanadaGeneral Alert
Patchwork and Pine Inc. Lip Balm and Artisan Soap recalled due to the presence of prohibited ingredients
Chemical hazard
Feb 17, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaAPO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
Drugs and health products
Health CanadaType II
APO-CANDESARTAN: Affected lots were manufactured using an active ingredient that was out of specification for dissolution
Product quality
Feb 16, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaSeasonique, Seasonale tablets: Affected lot(s) may not contain the correct amount of tablets (missing blister card)
Drugs and health products
Health CanadaType I
Seasonique, Seasonale tablets: Affected lot(s) may not contain the correct amount of tablets (missing blister card)
Product quality
Feb 13, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaHydromassage Rotary jets recalled due to potential Entrapment and Drowning Hazards
Consumer product safety
Health CanadaGeneral Alert
Hydromassage Rotary jets recalled due to potential Entrapment and Drowning Hazards
Entrapment hazard - Drowning hazard
Feb 12, 2026Consumer product safety
Medical DeviceFDA Devices
FDA DevicesProduct Name: Single Use Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC431Q-0720 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Olympus Corporation of the Americas
FDA DevicesClass II
Product Name: Single Use Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC431Q-0720 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Devices which did not undergo thermoforming could deform and lose performance.
Feb 11, 2026Olympus Corporation of the Americas
Medical DeviceFDA Devices
FDA DevicesProduct Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Olympus Corporation of the Americas
FDA DevicesClass II
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3025 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Devices which did not undergo thermoforming could deform and lose performance.
Feb 11, 2026Olympus Corporation of the Americas
Medical DeviceFDA Devices
FDA DevicesPRIMSAFLEX M100 SET, Product Code 106697; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
FDA DevicesClass II
PRIMSAFLEX M100 SET, Product Code 106697; Dialyzer, High Permeability With Or Without Sealed Dialysate System
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Feb 11, 2026VANTIVE US HEALTHCARE LLC
Medical DeviceFDA Devices
FDA DevicesProduct Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0730 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Olympus Corporation of the Americas
FDA DevicesClass II
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-411Q-0730 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Devices which did not undergo thermoforming could deform and lose performance.
Feb 11, 2026Olympus Corporation of the Americas
Medical DeviceFDA Devices
FDA DevicesProduct Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0725; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Olympus Corporation of the Americas
FDA DevicesClass II
Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0725; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Devices which did not undergo thermoforming could deform and lose performance.
Feb 11, 2026Olympus Corporation of the Americas
Food & BeverageFDA Food
FDA FoodCINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC venzutraders@outlook.com
VENZU TRADERS LLC
FDA FoodClass II
CINNAMON POWDER NET WT : 3.5 oz (100g) PRODUCT OF INDIA UPC 7 46241 29537 8 Distributed by: Venzu Traders LLC venzutraders@outlook.com
Potential contamination with heavy metal (lead).
Feb 11, 2026VENZU TRADERS LLC
Medical DeviceFDA Devices
FDA DevicesPRISMAFLEX ST100 SET US, Product Code 107636US; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
FDA DevicesClass II
PRISMAFLEX ST100 SET US, Product Code 107636US; Dialyzer, High Permeability With Or Without Sealed Dialysate System
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Feb 11, 2026VANTIVE US HEALTHCARE LLC
Medical DeviceFDA Devices
FDA DevicesOXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without Sealed Dialysate System
VANTIVE US HEALTHCARE LLC
FDA DevicesClass II
OXIRIS SET, Product Code 112016; Dialyzer, High Permeability With Or Without Sealed Dialysate System
There is a potential dislodgement of the Prismaflex Set deaeration chamber from the Prismaflex Control Unit.
Feb 11, 2026VANTIVE US HEALTHCARE LLC