Safety Recall Directory
Browse and filter the latest official safety alerts globally.
RappelConsods automobiles - ds3 crossback, ds4 v2 voiture particulière
ds automobiles - ds3 crossback, ds4 v2 voiture particulière
le véhicule peut présenter une fuite de carburant dans le tuyau à haute pression, entre la pompe à haute pression et le rail, en raison de l'absence d'écrou. cela peut provoquer un incendie dans le véhicule.
RappelConsojeep - avenger voiture particulière
jeep - avenger voiture particulière
le véhicule peut présenter une fuite de carburant dans le tuyau à haute pression, entre la pompe à haute pression et le rail, en raison de l'absence d'écrou. cela peut provoquer un incendie dans le véhicule.
RappelConsofiat - 600, grande panda voiture particulière
fiat - 600, grande panda voiture particulière
le véhicule peut présenter une fuite de carburant dans le tuyau à haute pression, entre la pompe à haute pression et le rail, en raison de l'absence d'écrou. cela peut provoquer un incendie dans le véhicule.
RappelConsopeugeot - ion voiture particulière
peugeot - ion voiture particulière
la structure des airbags du conducteur et du passager avant peut se détériorer. si les airbags se déploient, des fragments du gonfleur pourraient blesser les occupants du véhicule.
RappelConsohoneywell miller - harnais
honeywell miller - harnais
un nombre limité de harnais de la série h500 pourraient avoir été assemblés avec un passage incorrect des sangles au niveau¤de l'anneau d sternal et/ou des boucles de cuisse, ce qui représente un risque grave pour la sécurité.
RappelConsochevrolet - aveo t300, cruze, orlando, trax voiture particulière
chevrolet - aveo t300, cruze, orlando, trax voiture particulière
le propulseur dans l'airbag du conducteur peut se détériorer avec le temps. si les airbags se déploient, des fragments du gonfleur peuvent blesser les occupants du véhicule.
RappelConsoford - tourneo connect, transit connect fourgonnette / véhicule utilitaire léger
ford - tourneo connect, transit connect fourgonnette / véhicule utilitaire léger
la caméra de recul peut geler donnant la fausse impression que la zone derrière le véhicule est claire, malgré la présence de personnes ou d'obstacles. cela peut augmenter le risque d'accident et de blessure. en outre, des messages d'avertissement tels que la défaillance du capteur de stationnement et les appels d'urgence peuvent être affichés dans le groupe d'instruments pendant le fonctionnement. les systèmes contrôlés par l'écran central, tels que le chauffage, le chauffage des sièges et la ventilation, peuvent également être inutilisables.
RappelConsocitroen - c4 ii voiture particulière
citroen - c4 ii voiture particulière
l'airbag peut se détériorer au fil du temps et, s'il est déployé, une pression interne excessive peut provoquer l'éclatement du corps du gonfleur et des fragments de métal pourraient traverser le matériau du coussin, causant des blessures aux occupants.
RappelConsomilin kervéguen - quinoa
milin kervéguen - quinoa
suspicion de présence de corps étranger dans le quinoa ( bris de verre)
FDA DevicesSQ40S Blood Transfusion Filter
SQ40S Blood Transfusion Filter
Due to products being released for distribution prior to completion of the required quality control release process the sterility assurance cannot be confirmed.
FDA DevicesRayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan 10B. Radiation Therapy Treatment Planning System
RayStation/RayPlan. Model/Catalog Number: 10.1. Software Version: RayStation/RayPlan 10B. Radiation Therapy Treatment Planning System
Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.
UK FSATHIS™ recalls THIS™ Isn’t Chicken Deli Pieces because of undeclared soya and wheat (gluten)
THIS™ recalls THIS™ Isn’t Chicken Deli Pieces because of undeclared soya and wheat (gluten)
Soya and Wheat (gluten) This product contains undeclared soya and wheat (gluten) making it a possible health risk for anyone with an allergy to soya and/or an allergy or intolerance to wheat or gluten or with coeliac disease.
FDA DevicesBrand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm
Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column Dist Radius Plate 6Hd/10Shaft/Left/Std/139mm Model/Catalog Number: 02.426.681S Product Description: 2 Column Distal Radius Plate - 6 Head, 10 Shaft, Standard Left - 139mm
The supplier manufactured anatomical left plates with an incorrect thread orientation.
NHTSAZero Motorcycles Inc. - Damaged Brake Hose May Leak
Zero Motorcycles Inc. - Damaged Brake Hose May Leak
A loss of brake pressure can reduce braking ability and cause a loss of vehicle control, increasing the risk of a crash.
NHTSAToyota Motor Engineering & Manufacturing - Unlocked Rear Door May Open Unexpectedly
Toyota Motor Engineering & Manufacturing - Unlocked Rear Door May Open Unexpectedly
A door that unexpectedly opens while the vehicle is moving increases the risk of injury.
FDA DevicesBrand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatment of pseudo folliculitis barbae on all skin types (Fitzpatrick I-VI). The process implies the generation of intense light pulses at specific wavelengths. The specific nature of the energies and pulse durations cause the desired effect (in the hair follicles and oxyhemoglobin in the blood) heating them sufficiently and destroying them without unnecessary damage to surrounding tissue. This is achieved by controlled emission of laser radiation to the target tissue. The system consists of a main console and two interchangeable applicators that delivers pulsed light in the range of 800-820nm with a peak in the 810nm in different spot sizes. Two of the applicators emitting radiation at 810 nm wavelength for two areas 13.5¿15 mm¿ and 14.5¿25.5 mm¿. Two different operation modes are available: static mode and dynamic mode, which are differentiated basically by the frequency range defined for each mode (1-4 Hz for static and 10 Hz for dynamic). The principle of operation consists in the photons travel along the axis and reflected again back into the crystal, continuing the chain reaction, while photons travelling in different directions leave the crystal. In one of the two mirrors, a tiny hole allows a small amount of light to leak out and the resulting beam is focused with lenses and is emitted from the laser. The total energy emitted by the Leaseir MHR Xcell is produced by an array of diodes. The laser emission is activated by the hand piece trigger, deliver a continuous pulse pattern while the button is pressed. Component: NO
Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatment of pseudo folliculitis barbae on all skin types (Fitzpatrick I-VI). The process implies the generation of intense light pulses at specific wavelengths. The specific nature of the energies and pulse durations cause the desired effect (in the hair follicles and oxyhemoglobin in the blood) heating them sufficiently and destroying them without unnecessary damage to surrounding tissue. This is achieved by controlled emission of laser radiation to the target tissue. The system consists of a main console and two interchangeable applicators that delivers pulsed light in the range of 800-820nm with a peak in the 810nm in different spot sizes. Two of the applicators emitting radiation at 810 nm wavelength for two areas 13.5¿15 mm¿ and 14.5¿25.5 mm¿. Two different operation modes are available: static mode and dynamic mode, which are differentiated basically by the frequency range defined for each mode (1-4 Hz for static and 10 Hz for dynamic). The principle of operation consists in the photons travel along the axis and reflected again back into the crystal, continuing the chain reaction, while photons travelling in different directions leave the crystal. In one of the two mirrors, a tiny hole allows a small amount of light to leak out and the resulting beam is focused with lenses and is emitted from the laser. The total energy emitted by the Leaseir MHR Xcell is produced by an array of diodes. The laser emission is activated by the hand piece trigger, deliver a continuous pulse pattern while the button is pressed. Component: NO
The console label for affected devices is missing the "DANGER" symbol.
FDA DevicesMEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
MEDLINE beds labeled as: 1) Semi Electric Basic Homecare Bed, REF MDR107002E; 2) Semi Electric Basic Homecare Bed, 4-pack,REF MDR107002E-4
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
FDA DevicesBrand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), temperature (TEMP), invasive pressure (IBP), Carbon Dioxide (CO2). The system capabilities include storing, displaying, analyzing and controlling such data afterwards. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. The system is intended to be used during patient transport inside and outside of the hospital environment. Component: No
Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM20 Product Description: The iM20 Patient Monitor System (hereinafter called iM20) can perform long-time continuous monitoring of multiple physiological parameters, including ECG, respiration (RESP), non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), temperature (TEMP), invasive pressure (IBP), Carbon Dioxide (CO2). The system capabilities include storing, displaying, analyzing and controlling such data afterwards. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. The system is intended to be used during patient transport inside and outside of the hospital environment. Component: No
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
FDA DevicesTego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Tego Connector: REF: 011-D1000, 01C-D1000, 055-D1000, D1000; Conector Tego: REF: LAT-D1000
Needle free access device intended as accessory to vascular access used in hemodialysis or accessory to intravascular administration sets has a silicone seal which may bulge at the top, separate from the body, tear; may result in fluid leaks, occluded fluid flow, inability to inject/withdraw blood product, delayed/interrupted therapy, exposure to biological contaminants, air infused into the body
FDA DevicesRifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.
Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.
Potential for fraying on the body support strap.
FDA DevicesMerit Medical , Custom Waste Management Kit Vascular Tray REF: K10T-05261
Merit Medical , Custom Waste Management Kit Vascular Tray REF: K10T-05261
Inflation device handle may detach from the syringe during procedure.
FDA DevicesMEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
MEDLINE beds labeled as: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.
FDA DevicesBrand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, including non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), and Quick TEMP/Infrared TEMP (TEMP). iM3 capabilities include storing, displaying measuring data. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. Component: No
Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, including non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), and Quick TEMP/Infrared TEMP (TEMP). iM3 capabilities include storing, displaying measuring data. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. Component: No
As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.
FDA DevicesRifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.
Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.
Potential for fraying on the body support strap.