Safety Recall Directory
Browse and filter the latest official safety alerts globally.
CPSCHuaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
Huaker Magnetic Balls and Rods Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violates the Small Ball Ban
The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.
RappelConsorayon charcuterie traditionnelle (plu 4927) - terrine au piment d'espelette
rayon charcuterie traditionnelle (plu 4927) - terrine au piment d'espelette
présence de listéria monocytogènes
CPSCJJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
JJGoo LED Balloon Lights Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
RappelConsocharcuteries issoldunoises - pate pomme deterre au bleu d'auvergne
charcuteries issoldunoises - pate pomme deterre au bleu d'auvergne
présence de listéria monocytogenes
RappelConsocochon de bretagne - pinbaz -saucisse sèche droite 250g
cochon de bretagne - pinbaz -saucisse sèche droite 250g
présence de salmonelle
RappelConsowhite rabbit - gummies thc 0,3%
white rabbit - gummies thc 0,3%
dépassement significatif du seuil réglementaire de delta-9-thc
RappelConsola ferme sainte colombe - produits laitiers
la ferme sainte colombe - produits laitiers
présence de listeria monocytogène
RappelConsobiocoop - riz au lait de brebis 2x120g
biocoop - riz au lait de brebis 2x120g
suspicion d'erreur d'emballage (étuis brebis utilisés pour conditionner des pots de riz au lait de vache)¤la mention vache est cependant bien précisée sur l'opercule des pots et correspond bien à leur contenu.
RappelConsomomotaro - s0047 momotaro miso ramen 12/465g(3pc) #18 wave
momotaro - s0047 momotaro miso ramen 12/465g(3pc) #18 wave
erreur de production - informations allergènes obsolètes
CPSCVive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
Vive Health Recalls Adult Portable Bed Rails Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
CPSCJoly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
Joly's Recalls 80% Vinegar Due to Risk of Serious Injury or Death from Poisoning and Chemical Burns; Violates FHSA Labeling Requirements
The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.
RappelConsoosito serie oro - kaki persimon osito serie oro espagne cat1 cal 10-12-14-16-18-20 lot 2900
osito serie oro - kaki persimon osito serie oro espagne cat1 cal 10-12-14-16-18-20 lot 2900
dépassement de lmr pour le lambda-cyhalothrine (?+?+s isomères). arfd 268.1%.
Health CanadaMonarch Platform
Monarch Platform
Performance
Australia ProductsThe Cooks Collective Culinary Professional Stand Mixer
The Cooks Collective Culinary Professional Stand Mixer
The product can generate or retain electric charge when used. The electric charge level exceeds the limit allowed under Australian electrical standards. As a result, the user can receive an electric shock if they simultaneously touch the beater shaft and the earthed metal enclosure.
Health CanadaBipolar Hugo RAS Systems
Bipolar Hugo RAS Systems
Performance
Australia ProductsCondor HMS Triple carabiners
Condor HMS Triple carabiners
The gate can malfunction and may not close automatically on affected carabiners when used.
Health CanadaBioFlo Dialysis Catheter With Endexo Technology
BioFlo Dialysis Catheter With Endexo Technology
Performance
FDA FoodSodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
Sodexo Stars Saccharin (Pink) Packets, Sugar Substitute, Net Wt 0.035 oz. (1g), Manufactured by Domino Foods, Inc., West Palm Beach, FL 33041
Undeclared Aspartame
FDA DevicesAzurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
FDA DevicesMedline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Medline medical convenience kits packaged as: MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B
Medline Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.
FDA DevicesMedline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
Health CanadaTransport Canada Recall - 2025030 - DUCATI
Transport Canada Recall - 2025030 - DUCATI
Brakes
Health CanadaTransport Canada Recall - 2026048 - BMW
Transport Canada Recall - 2026048 - BMW
Lights And Instruments
Health CanadaTrilogy EVO and EV300
Trilogy EVO and EV300
Device compatibility