Safety Recall Directory
Browse and filter the latest official safety alerts globally.
Health CanadaKollide Magnet Game recalled due to ingestion hazard
Kollide Magnet Game recalled due to ingestion hazard
Ingestion hazard
Health CanadaMedline Neuro Sponges
Medline Neuro Sponges
Sterility
Health CanadaHEAD Alpine Ski Boots recalled due to injury hazard
HEAD Alpine Ski Boots recalled due to injury hazard
Injury hazard
Health CanadaTransport Canada Recall - 2026150 - PREVOST
Transport Canada Recall - 2026150 - PREVOST
Seats And Restraints
Health CanadaTransport Canada Recall - 2026175 - TOYOTA
Transport Canada Recall - 2026175 - TOYOTA
Fuel System
Health CanadaNucletron B.V. Intrauterine Tube
Nucletron B.V. Intrauterine Tube
Performance
Health CanadaMedline ENFit G-Tube Connector
Medline ENFit G-Tube Connector
Device compatibility
Health CanadaTransport Canada Recall - 2026146 - TRIUMPH
Transport Canada Recall - 2026146 - TRIUMPH
Lights And Instruments
Health CanadaTransport Canada Recall - 2026147 - MERCEDES-BENZ
Transport Canada Recall - 2026147 - MERCEDES-BENZ
Airbag
Health CanadaTransport Canada Recall - 2026174 - FOREST RIVER
Transport Canada Recall - 2026174 - FOREST RIVER
Label
Health CanadaCertain cheese products recalled due to Listeria monocytogenes
Certain cheese products recalled due to Listeria monocytogenes
Listeria
FDA DevicesAllura Xper FD20/15; System Code: 722058;
Allura Xper FD20/15; System Code: 722058;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DeviceseTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
eTRAX Needle Sensor - 14G(for Aurora Trackers), Part Number 667-157
There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.
FDA DevicesALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DevicesMiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
MiniMed 700G Insulin Pump (MMT-1801, MMT-1805, MMT-1850, MMT-1851)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
FDA DevicesAllura Xper FD10C; System Code: 722001;
Allura Xper FD10C; System Code: 722001;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA Devices2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
FDA DevicesCardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.
FDA DevicesALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DevicesAllura Xper FD20/20; System Code: 722038;
Allura Xper FD20/20; System Code: 722038;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DevicesALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DevicesAzurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
FDA DevicesBurlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
Burlington Medical, BAT (Breast, Axilla and Thyroid) Coverage.
Potential for attenuation degradation over time, decreasing the lifespan.
FDA DevicesBrand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use. All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient). Component: NA
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp endoscopic dissectors, scissors, scalpels, forceps/pick-ups, needle holders, endoscopic retractors, electrocautery and accessories are intended for endoscopic manipulation of tissue, including grasping, cutting, blunt and sharp dissection, approximation, ligation, electrocautery, suturing, and delivery and placement of microwave and cryogenic ablation probes and accessories. Please refer to attached User Manual for additional details on intended use. All da Vinci S/Si reusable instruments with jaws use mechanical tungsten cables and pulleys to transmit motion from the input discs to the housing (on the proximal chassis), through the main shaft, and the distal instrument tip (inside the patient). Component: NA
Due to increased complaints for broken/frayed grip cables for reusable instruments.