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Safety Alert
Health Canada
Health CanadaTransport Canada Recall - 2026174 - FOREST RIVER
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026174 - FOREST RIVER
Label
Apr 8, 2026TC
Pharmaceutical
FDA Drugs
FDA DrugstraMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382220, India, Distributed by: Amneal Pharmaceuticals LLC, Glasgow, KY 42141, NDC 60219-2348-5.
Amneal Pharmaceuticals, LLC
FDA DrugsClass II
traMADol Hydrochloride Tablets, USP, 50 mg, 500-count bottles, Rx only, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad 382220, India, Distributed by: Amneal Pharmaceuticals LLC, Glasgow, KY 42141, NDC 60219-2348-5.
Failed Impurities/Degradation Specifications: N-nitroso-desmethyl-tramadol impurity (NDSRI) was found out of the specification at 24-month stability interval during Long term stability (25¿C/60%RH).
Apr 8, 2026Amneal Pharmaceuticals, LLC
Safety AlertHealth Canada
Health CanadaCertain cheese products recalled due to Listeria monocytogenes
CFIA
Health CanadaClass 1
Certain cheese products recalled due to Listeria monocytogenes
Listeria
Apr 8, 2026CFIA
Safety AlertHealth Canada
Health CanadaNucletron B.V. Intrauterine Tube
Medical devices
Health CanadaType II
Nucletron B.V. Intrauterine Tube
Performance
Apr 8, 2026Medical devices
Safety AlertHealth Canada
Health CanadaMedline ENFit G-Tube Connector
Medical devices
Health CanadaType II
Medline ENFit G-Tube Connector
Device compatibility
Apr 8, 2026Medical devices
Medical DeviceFDA Devices
FDA DevicesMiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Medtronic MiniMed, Inc.
FDA DevicesClass II
MiniMed 720G Insulin Pump (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
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.
Apr 8, 2026Medtronic MiniMed, Inc.
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026146 - TRIUMPH
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026146 - TRIUMPH
Lights And Instruments
Apr 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026150 - PREVOST
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026150 - PREVOST
Seats And Restraints
Apr 8, 2026TC
Safety AlertHealth Canada
Health CanadaTransport Canada Recall - 2026147 - MERCEDES-BENZ
TC
Health CanadaGeneral Alert
Transport Canada Recall - 2026147 - MERCEDES-BENZ
Airbag
Apr 8, 2026TC
Food & BeverageFDA Food
FDA FoodPOPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
Pocas International Corp.
FDA FoodClass III
POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
Apr 8, 2026Pocas International Corp.
Medical DeviceFDA Devices
FDA DevicesAzurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Apr 8, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Food & Beverage
RappelConso
RappelConsosimulation réaliste en peluche chien intelligent appelé marche en peluche jouet électrique jouet souple
Unknown Firm
RappelConsoGeneral Alert
simulation réaliste en peluche chien intelligent appelé marche en peluche jouet électrique jouet souple
les piles peuvent surchauffer si les parties mobiles du jouet mou (jambes et tête) sont obstruées pendant l'utilisation standard, ce qui peut causer des brûlures aux utilisateurs.
Apr 8, 2026
Medical DeviceFDA Devices
FDA DevicesOXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Oxoid Australia Pty Limited
FDA DevicesClass II
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.
Apr 8, 2026Oxoid Australia Pty Limited
Medical DeviceFDA Devices
FDA DevicesSterile Radiology Procedure Kits, Model Number DYNDH1491B
Medline Industries, LP
FDA DevicesClass II
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.
Apr 8, 2026Medline Industries, LP
Medical DeviceFDA Devices
FDA DevicesArtoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
Mentor Texas, LP.
FDA DevicesClass II
Artoura Breast Tissue Expanders Reference Numbers: TEXP110RH TEXP120RH TEXP120RUH TEXP130RH TEXP135RH TEXP140RH TEXP150RH Textured, High & Ultra High Profile, Integral Injection Dome, 300cc, 375cc, 535cc, 475cc, 500cc, 600cc, 750cc,
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Apr 8, 2026Mentor Texas, LP.
Medical DeviceFDA Devices
FDA DevicesBrand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 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
Intuitive Surgical, Inc.
FDA DevicesClass II
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 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.
Apr 8, 2026Intuitive Surgical, Inc.
Food & BeverageFDA Food
FDA FoodMEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; UPC: 6912449124329
Super World Trading Inc.
FDA FoodClass III
MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; UPC: 6912449124329
Products contain cyclamates (banned sweetener)
Apr 8, 2026Super World Trading Inc.
Medical DeviceFDA Devices
FDA DevicesCPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
Mentor Texas, LP.
FDA DevicesClass II
CPX 4 US Breast Tissue Expanders with Suture Tabs Reference Numbers: SCPX-107MH, SCPX-117MH,SCPX-127MH, SCPX-135MH, SCPX-146MH, SCPX-156MH Smooth Medium Height Tissue Expander, 275cc, 350cc, 450cc, 550cc, 650cc, 800cc
Infusion sets may contain dull/blunt needle tip, which may be difficult to advance, and/or break.
Apr 8, 2026Mentor Texas, LP.
Medical DeviceFDA Devices
FDA DevicesBurlington Medical, Kilt
Burlington Medical, LLC
FDA DevicesClass II
Burlington Medical, Kilt
Potential for attenuation degradation over time, decreasing the lifespan.
Apr 8, 2026Burlington Medical, LLC
Food & BeverageFDA Food
FDA FoodPOPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ
Pocas International Corp.
FDA FoodClass III
POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
Apr 8, 2026Pocas International Corp.
Medical DeviceFDA Devices
FDA DevicesBurlington Medical, Caps.
Burlington Medical, LLC
FDA DevicesClass II
Burlington Medical, Caps.
Potential for attenuation degradation over time, decreasing the lifespan.
Apr 8, 2026Burlington Medical, LLC
Medical DeviceFDA Devices
FDA DeviceseTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
Civco Medical Instruments Co. Inc.
FDA DevicesClass II
eTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
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.
Apr 8, 2026Civco Medical Instruments Co. Inc.
Medical DeviceFDA Devices
FDA DevicesBrand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 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
Intuitive Surgical, Inc.
FDA DevicesClass II
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 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.
Apr 8, 2026Intuitive Surgical, Inc.
Medical DeviceFDA Devices
FDA DevicesBrand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon length 225mm, catheter working length 150cm Component: NA
SUMMA THERAPEUTICS, LLC
FDA DevicesClass II
Brand Name: Finesse BTK Multicath Product Name: Injectable Angioplasty Balloon Catheter Model/Catalog Number: FS252251502 Product Description: 5 French sheath, 0.014" guidewire compatible over-the-wire injectable angioplasty balloon catheter, balloon diameter 2.5mm, balloon length 225mm, catheter working length 150cm Component: NA
Potential for the balloon in the device to not meet burst specifications.
Apr 8, 2026SUMMA THERAPEUTICS, LLC