Safety Recall Directory
Browse and filter the latest official safety alerts globally.
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 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 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 DevicesAllwell Inflation Device, for angiographic use REF: IS-30-A
Allwell Inflation Device, for angiographic use REF: IS-30-A
Inflation device handle may detach from the syringe during procedure.
UKField Safety Notices: 19 to 23 January 2026
Field Safety Notices: 19 to 23 January 2026
List of Field Safety Notices from 19 to 23 January 2026....
UKClass 4 Medicines Defect Notification: Blumont Pharma Limited, Ocumont Eye Ointment 1% w/w, EL(26)A/03
Class 4 Medicines Defect Notification: Blumont Pharma Limited, Ocumont Eye Ointment 1% w/w, EL(26)A/03
Blumont Pharma Limited is reporting to the MHRA regarding the absence of Braille on the outer carton of one batch of Ocumont Eye Ointment 1% w/w (POM). It was identified that the Braille information w...
UKMHRA Safety Roundup: January 2026
MHRA Safety Roundup: January 2026
Summary of the latest safety advice for medicines and medical device users...
AustraliaNew Presolol (labetalol) tablet shortage: substitution instrument and overseas-registered alternative approved
New Presolol (labetalol) tablet shortage: substitution instrument and overseas-registered alternative approved
PRESOLOL 200 TABLET SHORTAGE HAS RESOLVED....
NHTSAHyundai Motor America - Instrument Panel Display Failure/FMVSS 101
Hyundai Motor America - Instrument Panel Display Failure/FMVSS 101
An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
NHTSAKia America, Inc. - Instrument Panel Display Failure/FMVSS 101, 138
Kia America, Inc. - Instrument Panel Display Failure/FMVSS 101, 138
An instrument panel display that fails to show critical safety information, such as the speedometer, tire pressure, or warning lights, increases the risk of a crash.
Health CanadaPolicom Mand'or brand Almond Hazelnut & Pistachio Drink recalled due to undeclared milk
Policom Mand'or brand Almond Hazelnut & Pistachio Drink recalled due to undeclared milk
Milk
Health CanadaGerber brand arrowroot biscuits recalled due to possible presence of pieces of soft plastic and paper
Gerber brand arrowroot biscuits recalled due to possible presence of pieces of soft plastic and paper
Extraneous Material
Health CanadaTransport Canada Recall - 2026025 - KEYSTONE
Transport Canada Recall - 2026025 - KEYSTONE
Structure
Health CanadaTransport Canada Recall - 2026008 - HYUNDAI
Transport Canada Recall - 2026008 - HYUNDAI
Lights And Instruments
Health CanadaTransport Canada Recall - 2026009 - RIVIAN
Transport Canada Recall - 2026009 - RIVIAN
Seats And Restraints
RappelConsola marque en moins - bio age 2 6-12 mois 800g
la marque en moins - bio age 2 6-12 mois 800g
principe de précaution suite aux nouvelles recommandations des autorités concernant la présence potentielle de céréulide.
RappelConsotoyota - proace max and proace max bev fourgonnette / véhicule utilitaire léger
toyota - proace max and proace max bev fourgonnette / véhicule utilitaire léger
lorsque le conducteur désactive et réactive le frein d'urgence automatique (aeb) au cours du même cycle de conduite, il reste désactivé sans qu'un voyant d'avertissement n'indique la désactivation. cela peut augmenter le risque d'accident.
RappelConsotoyota - proace and proace verso fourgonnette / véhicule utilitaire léger
toyota - proace and proace verso fourgonnette / véhicule utilitaire léger
les véhicules peuvent avoir une corrosion excessive sur le boulon du bras de suspension avant, en raison de la conception en combinaison avec des facteurs environnementaux. en conséquence, le boulon peut tomber en panne, ce qui peut affecter la contrôlabilité du véhicule et augmenter le risque d'accident.
RappelConsomes p'tits cubes - bonbons a l'extrait de chanvre full spectrum
mes p'tits cubes - bonbons a l'extrait de chanvre full spectrum
une consommation journalière excessive peut dépasser la dose aiguë de référence en ?9-thc.
RappelConsola marque en moins - bio age 1 0-6 mois 800g
la marque en moins - bio age 1 0-6 mois 800g
principe de précaution suite aux nouvelles recommandations des autorités concernant la présence potentielle de céréulide.
RappelConsola marque en moins - bio age 3 10-36 mois 800g
la marque en moins - bio age 3 10-36 mois 800g
principe de précaution suite aux nouvelles recommandations des autorités concernant la présence potentielle de céréulide.
RappelConsotoyota - proace, proace verso, proace city and proace city verso fourgonnette / véhicule utilitaire léger
toyota - proace, proace verso, proace city and proace city verso fourgonnette / véhicule utilitaire léger
une erreur d'étalonnage dans le logiciel de l'unité de commande électronique du moteur (ecu) peut empêcher le voyant de dysfonctionnement (mil) de s'activer lorsque le système de réduction catalytique sélective (scr) et / ou le filtre à particules diesel (dpf) tombe en panne, risquant des défauts non détectés et entraînant des émissions supérieures aux limites réglementaires.
UK FSALidl GB recalls Red Hen Gastro 2 Southern Fried Chicken Thigh Burgers because celery is not emphasised on the label
Lidl GB recalls Red Hen Gastro 2 Southern Fried Chicken Thigh Burgers because celery is not emphasised on the label
Celery This product contains celery making it a possible health risk for anyone with an allergy to celery.
RappelConsorubies - deguisement alien vert
rubies - deguisement alien vert
le produit est apparu non-conforme et dangereux, au regard de la norme nf en 71-3 : dépassement des limites de migration cr vi sur¤les étiquettes de marquage, et au regard de la norme nf en 71-1 point 5.2 : accessibilité au rembourrage