Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Health CanadaHemodialysis Opening (Hemodialyse Ouverture) Packs
Hemodialysis Opening (Hemodialyse Ouverture) Packs
Performance
Health CanadaPTI brand Besan Chick Pea Flour recalled due to the presence of insects
PTI brand Besan Chick Pea Flour recalled due to the presence of insects
Extraneous Material
Health CanadaTransport Canada Recall - 2026011 - WINNEBAGO INDUSTRIES
Transport Canada Recall - 2026011 - WINNEBAGO INDUSTRIES
Electrical
Health CanadaTransport Canada Recall - 2026012 - LUCID MOTORS, INC.
Transport Canada Recall - 2026012 - LUCID MOTORS, INC.
Visual System
Health CanadaVITEK® 2 Systems
VITEK® 2 Systems
Performance
Health CanadaNûby IcyBite™ Keys Teethers recalled due to microbial contamination
Nûby IcyBite™ Keys Teethers recalled due to microbial contamination
Microbial hazard
NHTSAKeystone RV Company - Ramp Door May Break During Use
Keystone RV Company - Ramp Door May Break During Use
A ramp door that breaks during use increases the risk of injury.
FDA DevicesPlum Duo Infusion System, List Number 40002-04-01
Plum Duo Infusion System, List Number 40002-04-01
ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo Infusion Pump fails, the pump may not produce audible alarms, alerts, or provide audible feedback for touchscreen inputs.
NHTSAVolkswagen Group of America, Inc. - Park Outside - High Voltage Battery May Catch Fire
Volkswagen Group of America, Inc. - Park Outside - High Voltage Battery May Catch Fire
A vehicle fire while parked or driving can increase the risk of injury.
NHTSAFord Motor Company - Inadequate Windshield Bonding/FMVSS 212
Ford Motor Company - Inadequate Windshield Bonding/FMVSS 212
In the event of a crash, windshield detachment can increase the risk of injury.
NHTSAOshkosh Corporation - Wheel May Detach from Vehicle
Oshkosh Corporation - Wheel May Detach from Vehicle
A detached wheel can cause a loss of vehicle control or become a road hazard for other vehicles, increasing the risk of a crash.
FDA DrugsDAYQUIL COLD & FLU, 32CT/2PK
DAYQUIL COLD & FLU, 32CT/2PK
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
FDA DevicesMedline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS, REF DYNJ908777B; 2) CARDIAC ROBOTIC WHC KIT-LF, REF DYNJ911359
Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a change in design in 2024, irrigation solution is able to travel to the handpiece and battery pack during use of the Strykeflow 2 Suction Irrigator. This design change has caused some devices to leak and/or emit vaporized saline (which can resemble smoke) during use.
FDA DevicesSMV BodyTrack, System, Tomography, Computed, Emission
SMV BodyTrack, System, Tomography, Computed, Emission
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
FDA DevicesSMV DSX New Line, System, Tomography, Computed, Emission
SMV DSX New Line, System, Tomography, Computed, Emission
GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
FDA DevicesAllura Xper FD20 OR Table; Model Number: 722023;
Allura Xper FD20 OR Table; Model Number: 722023;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
FDA DevicesFreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results
RappelConsopicot - picot laits infantiles en poudre
picot - picot laits infantiles en poudre
rappel volontaire : présence potentielle de céréulide dans un ingrédient (l’oméga 6 ara) provenant d’un fournisseur international et rentrant dans la composition de certains laits infantiles.
RappelConsopicot - picot laits infantiles en poudre
picot - picot laits infantiles en poudre
rappel volontaire : présence potentielle de céréulide dans un ingrédient (l’oméga 6 ara) provenant d’un fournisseur international et rentrant dans la composition de certains laits infantiles.
RappelConsoel manar - sardines huile d'olive 125g x12 el manar
el manar - sardines huile d'olive 125g x12 el manar
taux d'histamine élevé (supérieur à 200mg/kg) dans une boîte de conserve de sardine - risque d'intoxication alimentaire
RappelConsolara - mangue tommy
lara - mangue tommy
limite maximale pour les pesticides dépassée
FDA FoodUkrop's 6" Pound Cake with Buttercream Icing/Red Roses NET WT 30 OZ (2.06lb/936g) UPC 7 22515 91452 7 and Ukrop's 8" Pound Cake with Buttercream Icing/Red Roses NET WT 44 OZ (2.75lb/1.25kg) UPC 7 22515 91456 5 CONTAINS: Egg, Milk, Wheat Made in a production area that also uses soy and tree nuts. Ukrop's Homestyle Foods, LLC Richmond, VA 23230
Ukrop's 6" Pound Cake with Buttercream Icing/Red Roses NET WT 30 OZ (2.06lb/936g) UPC 7 22515 91452 7 and Ukrop's 8" Pound Cake with Buttercream Icing/Red Roses NET WT 44 OZ (2.75lb/1.25kg) UPC 7 22515 91456 5 CONTAINS: Egg, Milk, Wheat Made in a production area that also uses soy and tree nuts. Ukrop's Homestyle Foods, LLC Richmond, VA 23230
Undeclared Soy. Label did not include soy, which was used in product.
FDA DrugsTESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical Technology, 132 South Central Avenue, Elmsford, NY 10523, NDC# 57377-100-01
TESTO-100 CIII (testosterone 100 mg), 10 Sterile Pellets per carton, Rx only, Manufactured by: Advanced Pharmaceutical Technology, 132 South Central Avenue, Elmsford, NY 10523, NDC# 57377-100-01
Lack of Assurance of Sterility: Potential microbial contamination of subcutaneous pellets.
FDA DevicesAllura Xper FD20; Model Number: 722028;
Allura Xper FD20; Model Number: 722028;
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.