Safety Recall Directory
Browse and filter the latest official safety alerts globally.
CPSCResistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym
Resistance Bands Recalled Due to Serious Injury from Impact Hazard; Imported by HomeProGym
The recalled resistance bands can forcefully separate from the handle during use, posing a risk of serious injury from impact hazard.
Health CanadaCincinnati Surgical Branded Blades And Scalpels
Cincinnati Surgical Branded Blades And Scalpels
Unauthorised device
Health CanadaLes Fermes Lufa brand Broccoli microgreens recalled due to pathogenic E. coli
Les Fermes Lufa brand Broccoli microgreens recalled due to pathogenic E. coli
E. Coli - other pathogenic
Health CanadaTransport Canada Recall - 2025614 - TOYOTA
Transport Canada Recall - 2025614 - TOYOTA
Engine
Health CanadaTransport Canada Recall - 2026221 - TESLA
Transport Canada Recall - 2026221 - TESLA
Visual System
Health CanadaHarmonyAIR A-Series Surgical Lighting System AND ALYON Surgical Lighting System
HarmonyAIR A-Series Surgical Lighting System AND ALYON Surgical Lighting System
Performance
Health CanadaNeurological Sponges
Neurological Sponges
Sterility
Health CanadaLIFEPAK 15 V4 SpCO/SpMet Sensors
LIFEPAK 15 V4 SpCO/SpMet Sensors
Performance
RappelConsocrece pelo - topical solution 5% minoxidil
crece pelo - topical solution 5% minoxidil
ce produit contient du minoxidil, une substance interdite dans la composition des produits cosmétiques (annexe ii, numéro d’ordre 372). il est reconnu non conforme et dangereux.¤
RappelConsofleurus - ma malle a sable colores
fleurus - ma malle a sable colores
présence d'amiante détectée dans un des tubes de sable.
RappelConsoleclerc langon - langue de porc
leclerc langon - langue de porc
présence de salmonelle
RappelConsocarrefour extra - steak hache pur boeuf surgele 15%mg
carrefour extra - steak hache pur boeuf surgele 15%mg
suspicion de présence de petits morceaux métalliques
RappelConsocrece pelo - spray tonic minoxidil+
crece pelo - spray tonic minoxidil+
ce produit contient du minoxidil, une substance interdite dans la composition des produits cosmétiques (annexe ii, numéro d’ordre 372). il est reconnu non conforme et dangereux.¤
RappelConsovegavero - moringa bio (2.000 mg)
vegavero - moringa bio (2.000 mg)
présence possible de salmonella
CPSCOrb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
Orb Funkee Squeeze Toys Recalled Due to Risk of Serious Injury or Death from Asbestos Exposure; Imported by The Orb Factory
The recalled Orb Funkee squeeze toys may contain fibrous tremolite (asbestos) in the sand, which can cause adverse health issues if inhaled.
CPSCLil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs
Lil Pick Up Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury or Death from Crash and Burn Hazards; Violates Mandatory Standard for ATVs
The recalled youth ATVs violate the federal mandatory ATV safety standard, posing a risk of serious injury or death. The youth ATVs fail to meet mechanical suspension requirements, and the reverse indicator light fails to illuminate, posing a crash hazard. The parking brakes fail to hold, posing a collision hazard. Additionally, the surfaces near the footwell can reach high temperatures, posing a risk of severe burns.
CPSCABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
ABC Trading Recalls Children's Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
The recalled children's toys violate the mandatory standard for toys because they contain button cell batteries and the compartments that hold the batteries can be easily accessed by children, posing a deadly ingestion hazard to children. When button cell and coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
CPSCBethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC
Bethlehem Lights Recalls Bethlehem Lights 10-inch Illuminated Ribbon Spheres Due to Risk of Serious Injury or Death from Fire Hazard; Sold by QVC
The LED lights on the recalled illuminated spheres can overheat, posing a risk of serious injury or death from a fire hazard.
FDA FoodFrederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the back of the bag is both lot number and a stamped expiration date. UPC 719283 357212; 12-9oz retail units per case.
Undeclared allergens (wheat and soy).
NHTSAAlliance RV, LLC - Battery Heating Pad May Overheat
Alliance RV, LLC - Battery Heating Pad May Overheat
The heating pad may overheat in the battery compartment, increasing the risk of a fire.
FDA DevicesLUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model Number: 99576 Catalog Number: 99576-000043 UDI-DI code: 00883873861875 LUCAS 3.1 Model Number: 99576 Catalog Number: 99576-000063 UDI-DI code: 00883873834329 LUCAS chest compression System is to be used for performing external cardiac compressions on adult patients who have acute circulatory arrest defined as absence of spontaneous breathing and pulse, and loss of consciousness.
Due to a subset of chest compression systems/devices where the service performed on the systems were not appropriately documented (The documents for the service performed to justify the passing results were not include in the service records).
FDA DevicesNamic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Namic Angiographic Manifold, custom, Medline Product Number/SKU 64038200; Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Medline has identified the presence of particulate within the fluid path of the Manifolds.
FDA DevicesRevolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
Revolution CT, x-ray computed tomography, Model Numbers 5590000 and 5590000-6
GE HealthCare has become aware of a potential security vulnerability impacting AW Server deployed via Edison Health Link (EHL) based CT Smart Subscription used in conjunction with certain Revolution Apex, Revolution Ascend, and Revolution CT systems.
FDA DevicesMedline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Number/SKU 60010508; 2. DBD-MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60160075; 3. CARDIAC CATH PACK, Medline Kit Number/SKU DYNJ04636N; 4. CATH LAB TRAY, Medline Kit Number/SKU DYNJ24250G; 5. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333D; 6. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333F; 7. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779G; 8. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779I; 9. CLOT RETRIEVAL PACK, Medline Kit Number/SKU DYNJ56140C; 10. TAVR PACK NO SYR, Medline Kit Number/SKU DYNJ62310C; 11. TAVR PACK, Medline Kit Number/SKU DYNJ62310D; 12. TAVR PACK, Medline Kit Number/SKU DYNJ62310F; 13. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911; 14. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911A; 15. CATH PACK, Medline Kit Number/SKU DYNJT6544; 16. LHK, Medline Kit Number/SKU NAM0015; 17. SLU LHK, Medline Kit Number/SKU SAMPC0706.
Medline medical convenience kits, containing Namic Manifold, Labeled as: 1. MTS,RT,HANDED/LFT,HRT,KIT, Medline Kit Number/SKU 60010508; 2. DBD-MTS,LEFT HEART,KIT, Medline Kit Number/SKU 60160075; 3. CARDIAC CATH PACK, Medline Kit Number/SKU DYNJ04636N; 4. CATH LAB TRAY, Medline Kit Number/SKU DYNJ24250G; 5. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333D; 6. CATH LAB PACK-LF, Medline Kit Number/SKU DYNJ38333F; 7. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779G; 8. CATH LAB ANGIOGRAPHY PACK, Medline Kit Number/SKU DYNJ50779I; 9. CLOT RETRIEVAL PACK, Medline Kit Number/SKU DYNJ56140C; 10. TAVR PACK NO SYR, Medline Kit Number/SKU DYNJ62310C; 11. TAVR PACK, Medline Kit Number/SKU DYNJ62310D; 12. TAVR PACK, Medline Kit Number/SKU DYNJ62310F; 13. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911; 14. DIAGNOSTIC 2 PACK, Medline Kit Number/SKU DYNJ81911A; 15. CATH PACK, Medline Kit Number/SKU DYNJT6544; 16. LHK, Medline Kit Number/SKU NAM0015; 17. SLU LHK, Medline Kit Number/SKU SAMPC0706.
Medline has identified the presence of particulate within the fluid path of the Manifolds.