États-Unis Recalls
Rappels de sécurité de la FDA, CPSC, NHTSA et de l’USDA FSIS.
CPSCFun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard
Fun and Function Recalls Children's Metal Multi-Point Swing Frames Due to Risk of Injury from Fall Hazard
The swing frames can crack or break during use, posing a fall hazard, which can result in injury.
CPSCSweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Sweetcrispy Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
CPSCnvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng
nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng
The protective pin mechanism on the Magic Pocket Staffs can fail to prevent unintentional expansion, posing serious projectile and laceration hazards. Even when engaged, the expansion occurs too rapidly for consumers to react, leaving virtually no opportunity for protection.
CPSCAdult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX
Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by ZOLIQUEX
The recalled bed rails violate the mandatory standard for adult portable bed rails because 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.
CPSCSanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids
Sanlebi Pet Vet Playsets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Letokids
The Pet Vet Playset violates the mandatory standard for toys because the button cell batteries in the nail grinder and otoscope can be easily accessed by children.
CPSCFengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Fengrong Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
CPSCApex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards
Apex Gaming PCs Recalls Manik and Apex-branded ATX Computer Power Supplies Due to Risk of Serious Injury or Death from Electrical Shock and Electrocution Hazards
The units lack a permanent, on-product warning label identifying potential electrical shock and electrocution hazards, posing a risk of serious injury or death if the unit is opened or disassembled.
CPSCFree-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel
Free-Standing Professional Gas Ranges Recalled Due to Risk of Burn Hazard; Manufactured by Fisher & Paykel
The ovens in the ranges can experience a delayed ignition, causing gas to accumulate and the oven door to open from combustion, posing a burn hazard to users.
CPSCAgiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Agiiman Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution.
CPSCMacy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard
Macy's Recalls Arch Studio Tea Kettles Due to Risk of Serious Injury from Burn Hazard
The tea kettles' handle can detach during use when heated, posing a risk of serious injury from burn hazard.
CPSCMini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART
Mini Round Toddler Trampolines Recalled Due to Strangulation Hazard; Risk of Serious Injury or Death; Manufactured by SEGMART
Young children can become entangled in the straps of the hammock, punching bag and hand ring accessories, posing a strangulation hazard, which can result in serious injury or death.
CPSCPressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Imported by BAYOTAK USA
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
CPSCJC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
JC Sales Recalls Lil' Buddies Pet Laser Toys Due to Risk of Serious Injury or Death from Battery Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries
The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.
CPSCATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US
ATOYUS Children's Activity Cubes Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Small Parts Ban and Mandatory Standard for Toys; Sold on Amazon by Melofaver US
The recalled toys violate the small parts ban because the toys are intended for children under three and the toys' xylophone screws and clock hands can detach. In addition, the toys violate the mandatory safety standard for children's toys because the mallets have spherical ends, posing a choking hazard.
CPSCLe Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
Le Hao Tool Recalls Pressure Washers Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and electrocution hazards.
CPSCMontessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower
Montessori Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking Hazard; Violate Mandatory Standard for Teething Toys; Sold on Amazon by SpringFlower
The Montessori toy sets contain an airplane shaped teething toy that has tentacle ends that can pose a choking hazard to young children. The toys also violate the teething toy provision of the mandatory standard for children's toys.
CPSCZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
ZMC Group Recalls LED Finger Beam Lights Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys
The recalled toys violate the mandatory safety standard for children's toys because the toy contains button cell batteries that can be easily accessed by children. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.
NHTSAChrysler (FCA US, LLC) - Engine Failure May Cause Fire or Loss of Drive Power
Chrysler (FCA US, LLC) - Engine Failure May Cause Fire or Loss of Drive Power
A loss of drive power increases the risk of a crash, and a vehicle fire increases the risk of injury.
CPSCGenerac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards
Generac Power Systems Recalls Portable Generators Due to Risk of Serious Injury or Death from Burn and Fire Hazards
When first filling the recalled generator with gasoline, fuel can leak from the carburetor, posing a risk of serious injury or death from fire or burn hazard. Consumers with generators that have previously been filled with enough gasoline to move the gauge off "E," or have been used without any gasoline leakage, can continue to be used.
FDA DevicesNAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
NAMIC Angiographic Control Syringe, labeled as follows: 1. SYRINGE,7ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70083007; 2. SYRINGE,8ML,TR/FR,RA,W/RES,-,P/G, Medline SKU 70084007; 3. MTS,SYRINGE,8ML,TR/FR,RA,NO,RES,-,P/G, Medline SKU 70084017; 4. SYRINGE,7,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80083007; 5. SYRINGE,8,ML,TR/FR,RA,W/RES,OEM,PG, Medline SKU 80084007; 6. MTO,SYRINGE,8,ML,TR/FR,RA,NO,RES,OEM,PG, Medline SKU 80084017.
Medline Industries, LP has identified through post-market surveillance a potential risk of the syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
FDA Drugs5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-458-05, Unit of Sale NDC Number: 65219-458-30.
5% Dextrose Injection, USP 12.5 g per 250 mL (50 mg per mL) 250 mL in a 250 mL freeflex bag, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Unit of Use NDC: 65219-458-05, Unit of Sale NDC Number: 65219-458-30.
Lack of Assurance of Sterility
FDA Drugs0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 63323-626-03, Unit of Sale NDC Number: 63323-626-25 (30 bags in 1 case).
0.45% Sodium Chloride Injection, USP, 1.125 grams per 250 mL (4.5 mg per mL), 250 mL in a 250 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 63323-626-03, Unit of Sale NDC Number: 63323-626-25 (30 bags in 1 case).
Lack of Assurance of Sterility
FDA Drugs0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-472-05, Unit of Sale NDC Number: 65219-472-20.
0.9% Sodium Chloride Injection, USP, (4,500 mg per 500 mL) (9 mg per mL) 500 mL in a 500 mL freeflex bag, Rx only, Fresenius Kabi USA, LLC ("Fresenius Kabi"), Lake Zurich, IL 60047, Unit of Use NDC: 65219-472-05, Unit of Sale NDC Number: 65219-472-20.
Lack of Assurance of Sterility
FDA DrugsLanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC 69097-906-67
Lanreotide Injection, 120 mg/0.5 mL, Box contains 1 Pre-filled syringe, Single dose only, Rx Only, Manufactured by: Pharmathen International, S.A., Rodopi, Greece. Manufactured for: Cipla USA, Inc., 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC 69097-906-67
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.