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Found 12,723 results for "product recalls and alerts"
Medical Device
FDA Devices
FDA DevicesBrand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.
Medartis AG
FDA DevicesClass II
Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable.
Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws.
Mar 18, 2026Medartis AG
Safety Alert
Health Canada
Health CanadaCertain Ajinomoto brand products recalled due to the possible presence of pieces of glass
CFIA
Health CanadaClass 2
Certain Ajinomoto brand products recalled due to the possible presence of pieces of glass
Extraneous Material
Mar 17, 2026CFIA
Safety AlertHealth Canada
Health CanadaDisinfectant Spray & Wipe Cleaner: Affected lots contain solution that do not meet the labelled strength
Drugs and health products
Health CanadaType II
Disinfectant Spray & Wipe Cleaner: Affected lots contain solution that do not meet the labelled strength
Product safety
Mar 17, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaHealth Canada warns that 2" Slats Wood Blinds for Indoor Windows previously available on Amazon.ca may pose risks of strangulation and choking
Consumer product safety
Health CanadaGeneral Alert
Health Canada warns that 2" Slats Wood Blinds for Indoor Windows previously available on Amazon.ca may pose risks of strangulation and choking
Choking hazard - Strangulation hazard
Mar 17, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaOut To Impress sand art and candles recalled due to possible asbestos contamination
Consumer product safety
Health CanadaGeneral Alert
Out To Impress sand art and candles recalled due to possible asbestos contamination
Chemical hazard
Mar 16, 2026Consumer product safety
Safety AlertHealth Canada
Health Canadae-NRG Bioethanol Fuel recalled due to flammability hazard
Consumer product safety
Health CanadaGeneral Alert
e-NRG Bioethanol Fuel recalled due to flammability hazard
Flammability hazard
Mar 16, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaVarious pistachios and pistachio-containing products recalled due to Salmonella
CFIA
Health CanadaClass 2
Various pistachios and pistachio-containing products recalled due to Salmonella
Salmonella
Mar 16, 2026CFIA
Safety AlertHealth Canada
Health CanadaTim Hortons Pink and White Colour Changing Donut Mug recalled due to a burn hazard
Consumer product safety
Health CanadaGeneral Alert
Tim Hortons Pink and White Colour Changing Donut Mug recalled due to a burn hazard
Burn hazard
Mar 16, 2026Consumer product safety
Food & BeverageUSDA FSIS
USDA FSISFSIS Issues Public Health Alert For Frozen Ready-To-Eat Turkey Stuffed Pastry Products Due To Misbranding
Shaw Bakers LLC
USDA FSISPublic Health A...
FSIS Issues Public Health Alert For Frozen Ready-To-Eat Turkey Stuffed Pastry Products Due To Misbranding
Misbranding
Mar 13, 2026Shaw Bakers LLC
Safety AlertHealth Canada
Health CanadaClore Beauty Supply products recalled due to missing mandatory hazard labelling
Consumer product safety
Health CanadaGeneral Alert
Clore Beauty Supply products recalled due to missing mandatory hazard labelling
Labelling and packaging
Mar 13, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaHealth Canada warns that PGST and GauTone Photoelectric Smoke Alarms previously available on AliExpress may fail to operate
Consumer product safety
Health CanadaGeneral Alert
Health Canada warns that PGST and GauTone Photoelectric Smoke Alarms previously available on AliExpress may fail to operate
Unauthorized products
Mar 13, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaModofo Tool 5 in 1 Smoke and Carbon Monoxide Detector recalled due to potential failure to operate
Consumer product safety
Health CanadaGeneral Alert
Modofo Tool 5 in 1 Smoke and Carbon Monoxide Detector recalled due to potential failure to operate
Unauthorized products
Mar 12, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaNitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
Drugs and health products
Health CanadaType I
Nitrous Oxide Chargers: Sold for Inhalation Without Market Authorization (DIN)
Product safety
Mar 12, 2026Drugs and health products
Safety AlertHealth Canada
Health CanadaCool Fidget Toy Stress Ball recalled due to ingestion hazard
Consumer product safety
Health CanadaGeneral Alert
Cool Fidget Toy Stress Ball recalled due to ingestion hazard
Ingestion hazard
Mar 12, 2026Consumer product safety
Safety AlertHealth Canada
Health CanadaSalt of the Earth Cedar and Amyris Replenish Cream recalled due to a chemical hazard
Consumer product safety
Health CanadaGeneral Alert
Salt of the Earth Cedar and Amyris Replenish Cream recalled due to a chemical hazard
Chemical hazard
Mar 12, 2026Consumer product safety
Pharmaceutical
UK
UKClass 3 Medicines Recall: Bayer Plc, Various Products, EL(26)A/12
Bayer Plc
uk-mhraMedicines Recall
Class 3 Medicines Recall: Bayer Plc, Various Products, EL(26)A/12
Bayer Plc is recalling all stock of the products listed in this notification as a precautionary measure due to the identification of an impurity above the acceptable limit. The recall is at pharmacy a...
Mar 12, 2026Bayer Plc
Food & BeverageFDA Food
FDA FoodJunebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), DRIED CHERRIES, ALMONDS; OAT FLOUR, COCOA POWDER, ORANGE ZEST, VANILLA EXTRACT (VANILLA BEAN EXTRACTIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUPMENT ALSO HANDLING PEANUT, SESAME. PRODUCED IN A FACILITY THAT ALSO PROCESES GLUTEN PRODUCTS. KEEP REFRIGERATED; UPC: 8 60012 38462 4
Juniper Granola, LLC
FDA FoodClass I
Junebar Chocolate Cherry All Natural Snack Bar; INGREDIENTS: ORGANIC ALMOND BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN CHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), DRIED CHERRIES, ALMONDS; OAT FLOUR, COCOA POWDER, ORANGE ZEST, VANILLA EXTRACT (VANILLA BEAN EXTRACTIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUPMENT ALSO HANDLING PEANUT, SESAME. PRODUCED IN A FACILITY THAT ALSO PROCESES GLUTEN PRODUCTS. KEEP REFRIGERATED; UPC: 8 60012 38462 4
Products contain undeclared milk and soy.
Mar 11, 2026Juniper Granola, LLC
Medical DeviceFDA Devices
FDA DevicesImpella RP Flex with SmartAssist. Product Code: 1000323.
Abiomed, Inc.
FDA DevicesClass I
Impella RP Flex with SmartAssist. Product Code: 1000323.
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Mar 11, 2026Abiomed, Inc.
Medical DeviceFDA Devices
FDA DevicesBrand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A
B Braun Medical Inc
FDA DevicesClass II
Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
Mar 11, 2026B Braun Medical Inc
Medical DeviceFDA Devices
FDA DevicesBrand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
Aesculap Inc
FDA DevicesClass II
Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
There is the potential for the length of the trocar shaft to be too long.
Mar 11, 2026Aesculap Inc
Medical DeviceFDA Devices
FDA DevicesImpella RP with SmartAssist. Product Code: 0046-0035.
Abiomed, Inc.
FDA DevicesClass I
Impella RP with SmartAssist. Product Code: 0046-0035.
Differential pressure (dP) sensor in Impella RP devices may malfunction, causing sensor values to drift.
Mar 11, 2026Abiomed, Inc.
Food & BeverageFDA Food
FDA FoodJunebar Peanut Chocolate Chip All Natural Snack Bar; INGREDIENTS: ORGANIC PEANUT BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN SHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), PEANUTS, OAT FLOUR, VANILLA EXTRACT (VANILLA BEAN EXTRATIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS PEANUTS, TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUIPMENT ALSO HANDLING PEANUT, SESAME, PRODUCED IN A FACILITY THAT ALSO PROCESSES GLUTEN PRODUCTS. KEEP REFRIGERATED.; UPC 8 60012 38461 7
Juniper Granola, LLC
FDA FoodClass I
Junebar Peanut Chocolate Chip All Natural Snack Bar; INGREDIENTS: ORGANIC PEANUT BUTTER, DATE PASTE, ORGANIC BLACK BEANS, ORGANIC SWEET POTATOES, GLUTEN FREE ROLLED OATS, SEMI-SWEET SOY FREE VEGAN SHOCOLATE CHIPS (ORGANIC CANE SUGAR, UNSWEETENED CHOCOLATE, COCOA BUTTER), PEANUTS, OAT FLOUR, VANILLA EXTRACT (VANILLA BEAN EXTRATIVES IN WATER, ALCOHOL), FLAX, CINNAMON, SEA SALT, BAKING POWDER; ALLERGEN WARNING: CONTAINS PEANUTS, TREE NUTS (ALMOND, COCONUT), PRODUCED ON EQUIPMENT ALSO HANDLING PEANUT, SESAME, PRODUCED IN A FACILITY THAT ALSO PROCESSES GLUTEN PRODUCTS. KEEP REFRIGERATED.; UPC 8 60012 38461 7
Products contain undeclared milk and soy.
Mar 11, 2026Juniper Granola, LLC
PharmaceuticalFDA Drugs
FDA DrugsMedi-First Antiseptic Wipes (BZK)(Benzalkonium Chloride 0.13%), 100 wipes per box, Manufactured for Medique Products, Fort Meyers, FL, 33967, NDC 47682-122-33.
ACME UNITED CORPORATION
FDA DrugsClass II
Medi-First Antiseptic Wipes (BZK)(Benzalkonium Chloride 0.13%), 100 wipes per box, Manufactured for Medique Products, Fort Meyers, FL, 33967, NDC 47682-122-33.
CGMP Deviations
Mar 11, 2026ACME UNITED CORPORATION
Medical DeviceFDA Devices
FDA DevicesBrand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog Number: SPL-SR, contains generator SPL-G Product Description: An assembly of devices that uses a combination of, or individually applied, pneumatically-created ballistic shock waves and ultrasonic waves for the intracorporeal fragmentation of stones (calculi) in the urinary tract (i.e., kidney, ureter, and bladder) for their removal. It typically includes a pressure and power regulator/control unit, handpieces, and two types of probes of various sizes. The probes are attached to the two handpieces which are connected to the control unit that supplies the energy for both the pneumatic and ultrasonic functions. Energy is applied to a calculus which is fragmented in situ and removed via a suction system facilitated by the lithotripsy system.
Olympus Corporation of the Americas
FDA DevicesClass II
Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog Number: SPL-SR, contains generator SPL-G Product Description: An assembly of devices that uses a combination of, or individually applied, pneumatically-created ballistic shock waves and ultrasonic waves for the intracorporeal fragmentation of stones (calculi) in the urinary tract (i.e., kidney, ureter, and bladder) for their removal. It typically includes a pressure and power regulator/control unit, handpieces, and two types of probes of various sizes. The probes are attached to the two handpieces which are connected to the control unit that supplies the energy for both the pneumatic and ultrasonic functions. Energy is applied to a calculus which is fragmented in situ and removed via a suction system facilitated by the lithotripsy system.
Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not consistent with electromagnetic compatibility (EMC) standards and may decrease the overall reliability of the system and result in delay of treatment. It was discovered that additional serial numbers of ShockPulse generators may also have the mis-wired component. As a result, this is expanding the action to the additional impacted devices.
Mar 11, 2026Olympus Corporation of the Americas