Vereinigte Staaten Recalls
Verbraucherrückrufe von FDA, CPSC, NHTSA und USDA FSIS.
CPSCWade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
Wade Logan Annyka 9-Drawer Fabric Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Imported by Ningbo Jiangdong Peter International Trading
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standard as required by the STURDY Act.
CPSCSDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
SDADI Kitchen Step Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by Yiwushi Bihe Trading
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.
CPSCJobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
Jobon Torch Lighters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards; Violate Mandatory Standard for Multipurpose Lighters
The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.
CPSCMNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
MNIENT Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails
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. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.
CPSCPanasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
Panasonic Recalls Electric Toaster Ovens Due to Shock and Fire Hazards
The power cord insulation can be insufficient due to a protective fiberglass sleeve not covering it adequately, posing a risk of shock and/or fire hazard.
CPSCMadewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
Madewell Recalls Women's Sweaters Due to Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Clothing Textiles
The recalled sweaters violate the mandatory standard for clothing textiles, posing a risk of serious burn injuries or death.
CPSCHuish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
Huish Outdoors Recalls Hollis Diving Regulators Due to Risk of Serious Injury or Death from Drowning
The regulator inlet tube can crack and break, posing a risk of serious injury or death from drowning.
CPSCOitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
Oitnlaughter Projecting Finger Light Toys Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys; Sold on Amazon by Delightmi
The recalled finger lights violate the mandatory safety standard for toys because they contain 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.
CPSCNoerishia 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 Hurzein
Noerishia 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 Hurzein
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.
NHTSAChrysler (FCA US, LLC) - Steel Wheels May Crack and Separate
Chrysler (FCA US, LLC) - Steel Wheels May Crack and Separate
Loss of vehicle control increases the risk of a crash.
NHTSAJaguar Land Rover North America, LLC - Water May Damage Rearview Camera
Jaguar Land Rover North America, LLC - Water May Damage Rearview Camera
A rearview camera image that does not display can decrease the driver's visibility, increasing the risk of a crash.
NHTSAInternational Motors, LLC - Body Panel Joints Incorrectly Attached/FMVSS 221
International Motors, LLC - Body Panel Joints Incorrectly Attached/FMVSS 221
The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.
NHTSANissan North America, Inc. - Incorrect GAWR on Certification Label/FMVSS 110
Nissan North America, Inc. - Incorrect GAWR on Certification Label/FMVSS 110
An overloaded vehicle can increase the risk of a crash.
NHTSAE-One Incorporated - Drive Mode May Disengage Causing a Loss of Drive Power
E-One Incorporated - Drive Mode May Disengage Causing a Loss of Drive Power
Loss of power to the rear wheels can prevent the vehicle from moving, increasing the risk of a crash.
NHTSAOrange EV - Frame Rails May Crack
Orange EV - Frame Rails May Crack
A detached rail can cause a loss of control, increasing the risk of injury.
FDA DevicesOmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
OmniTract Surgical Retractor System, which includes 633 of the firm s product codes.
The current Omni-Tract Surgical Retractor System IFU states a dry time of 30 minutes. Integra LifeSciences has identified that the dry time needs to be extended to 90 minutes, 110 minutes, or 120 minutes depending on the sterilization cycle exposure time used.
FDA DevicesMedline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569D; 2) ACCESSORY KIT, Model Number: DYNJ901348F
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
FDA DevicesBrand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 341-14-711 Product Description: Enovis knee devices are for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
FDA DevicesBrand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Brand Name: EMPOWR 3D KNEE Product Name: EMPOWR 3D KNEE INS, 11L 14MM, VE Model/Catalog Number: 342-19-703 Product Description: Enovis knee devices are intended for knee arthroplasty.
Due to packaging discrepancy with incorrect product size mixed up.
FDA DevicesMedline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Medline Convenience Kits: 1) OPEN HEART PEDS PACK, Model Number: DYNJ88569; 2) OPEN HEART PEDS PACK, Model Number: DYNJ88569A; 3) OPEN HEART PEDS PACK, Model Number: DYNJ88569B; 4) OPEN HEART PEDS PACK, Model Number: DYNJ88569C
Convenience Kits contain Covidien Mon-a-Therm General Purpose Temperature Probes Size 9 Fr. Medtronic has issued a recall of specific production lots of the Covidien Mon-a-Therm general purpose temperature probe-size 9 due to an error in its distribution control process.
FDA DevicesIntracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS INSTRUMENTS- DRILL EU/RLV0035-EU, INTRACEPT ACCESS INSTRUMENTS- 2VB/RLV0045, INTRACEPT ACCESS INSTRUMENTS- 2VB EU/RLV0045-EU, INTRACEPT ACCESS INSTRUMENTS- 3VB/RLV0055, INTRACEPT ACCESS INSTRUMENTS- 3VB EU/RLV0055-EU, INTRACEPT ACCESS INSTRUMENTS 2 VB/RLV0065, INTRACEPT ACCESS INSTRMNTS ADDITIONAL VB/RLV0075, INTRACEPT ACCESS INSTRMNTS ADDTL VB EU/RLV0075-EU
Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if breached could lead to severe infection.
FDA DevicesVITEK 2 AST-N447 TEST KIT Product reference 424620
VITEK 2 AST-N447 TEST KIT Product reference 424620
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
FDA DevicesTMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components
TMINI Femur Tracking Array REF 109003 UDI-DI code: M9461090030 TMINI Tibia Tracking Array REF 109004 UDI-DI code: M9461090040 TMINI Miniature Robotic System is indicated as a stereotaxic instrumentation system for total knee replacement (TKA) surgery. It is to assist the surgeon by providing software-defined spatial boundaries for orientation and reference information to identifiable anatomical structures for the accurate placement of knee implant components
Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array.
FDA DevicesBrand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Brand Name: Geneva Product Name: Brachytherapy Applicator Product Description: The device is intended for intracavitary brachytherapy for cancer treatment of the cervix and the endometrium. Optional needles can be placed for interstitial therapy.
Due to safety concerns regarding the detachment of the tip of the intrauterine tube (IU tube) that may remain within a patient.