Safety Recall Directory
Browse and filter the latest official safety alerts globally.
RappelConsoluna sweet - perle de tapioca lait de coco, pudding aux graines de chia mangue
luna sweet - perle de tapioca lait de coco, pudding aux graines de chia mangue
détection listeria dans l'environnement de fabrication¤
RappelConsoauchan le poissonnier - filet de maquereau sous vide
auchan le poissonnier - filet de maquereau sous vide
suite à la détection d'histamine
RappelConsomarque : mdh peacock - kasoori methi (feuilles de fenugrec séchées)
marque : mdh peacock - kasoori methi (feuilles de fenugrec séchées)
il a été constater que cet article contient des pesticides
RappelConsoyerba mate elaborada amanda - yerba mate
yerba mate elaborada amanda - yerba mate
présence d'une quantité de pesticide anthraquinone supérieure à la réglementation en vigueur.
RappelConso- - masques de carnaval
- - masques de carnaval
un contrôle a mis en évidence l’absence de mise en relief de l’allergène lait dans la liste d’ingrédients du produit.
RappelConsocollier chaine os de serpent pour femmes ensemble de colliers
collier chaine os de serpent pour femmes ensemble de colliers
le produit a une concentration excessive de plomb (valeur mesurée: 2,6 % en poids). le plomb est nocif pour la santé humaine, s'accumule dans le corps, peut induire une neurotoxicité pour le développement et peut également nuire aux enfants à naître ou allaités. le taux de libération de nickel est trop élevé (valeur mesurée jusqu'à 3,2 µg/cm2/semaine). le nickel est un sensibilisant fort et provoque des réactions allergiques s'il est présent dans des articles qui entrent en contact direct et prolongé avec la peau.
RappelConsogona la paix - gona la paix
gona la paix - gona la paix
présence de sildénafil (substance active médicamenteuse interdite dans les aliments).
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 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 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.
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 DevicesAzurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
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 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 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 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 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.
Health CanadaACE Surgical Supply® PGA (Polyglycolic Acid) Absorbable Sutures & Absorbable Gut Sutures
ACE Surgical Supply® PGA (Polyglycolic Acid) Absorbable Sutures & Absorbable Gut Sutures
Unauthorised device
FDA FoodImu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins, CO 80524.
Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins, CO 80524.
Product is potentially under-processed.
RappelConsosimulation réaliste en peluche chien intelligent appelé marche en peluche jouet électrique jouet souple
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.
FDA DevicesOXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
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.
FDA DevicesBurlington Medical, Half Aprons.
Burlington Medical, Half Aprons.
Potential for attenuation degradation over time, decreasing the lifespan.
FDA DeviceseTRAX Needle System Starter Kit 12G (for Aurora Trackers), Part Number 667-149
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.
FDA DevicesAllura Xper FD20/20 OR Table; System Code: 722039;
Allura Xper FD20/20 OR Table; System Code: 722039;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.