Estados Unidos Recalls
Retiros de seguridad del consumidor de la FDA, CPSC, NHTSA y USDA FSIS.
NHTSAInternational Motors, LLC - Body Panel Joint Incorrectly Attached/FMVSS 221
International Motors, LLC - Body Panel Joint Incorrectly Attached/FMVSS 221
The body panels may separate during a crash, reducing structural integrity and increasing the risk of injury.
NHTSATerex South Dakota, Inc. - Cracked Weld May Cause Pole Guide Arm to Fall
Terex South Dakota, Inc. - Cracked Weld May Cause Pole Guide Arm to Fall
Without a retaining pin, the pole guide arm may fall, increasing the risk of injury to people around the truck.
NHTSALippert - Incorrect Seal Used on Axle During Assembly
Lippert - Incorrect Seal Used on Axle During Assembly
A loss of lubrication can cause bearing failure and wheel loss, increasing the risk of a crash.
CPSCWagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard
Wagner Spray Tech Recalls 900 Series Power Steamers Due to Burn Hazard
The attached hose can get excessively hot and the nozzle/gun can expel hot water during use and after the trigger is engaged, posing a serious burn hazard to consumers.
CPSCElectrolux Group Recalls Frigidaire Gas Ranges Due to Burn Hazard
Electrolux Group Recalls Frigidaire Gas Ranges Due to Burn Hazard
The ovens in the ranges can experience a delayed ignition of the oven's bake burner, posing a risk of burn hazards to users.
CPSCTainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard
Tainoki Fine Furniture Recalls Office Chairs Due to Risk of Serious Injury and Fall Hazard
The recalled chairs' base can bend, posing a fall hazard.
CPSCInfant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store
Infant Walkers Recalled Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers; Sold on Amazon by Goregent Official Store
The recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a risk of serious injury or death due to a fall hazard.
CPSCLifetime Brands Recalls BUILT LUUM Light Up Tumblers Due to Risk of Choking and Battery Ingestion Hazards
Lifetime Brands Recalls BUILT LUUM Light Up Tumblers Due to Risk of Choking and Battery Ingestion Hazards
The recalled LED tumblers can break, making the button cell batteries accessible to children and posing choking and ingestion hazards. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
CPSCAisstxoer Adult Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by YXTDZ Store
Aisstxoer Adult Bicycle Helmets Recalled Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets; Sold on Amazon by YXTDZ Store
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the impact attenuation, positional stability, and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
CPSCSpecialized Bicycle Components Recalls Specialized Turbo Como SL Electric Bicycles Due to Risk of Serious Injury or Death from Fall Hazard
Specialized Bicycle Components Recalls Specialized Turbo Como SL Electric Bicycles Due to Risk of Serious Injury or Death from Fall Hazard
The bike's fork steerer tube can develop a small fatigue crack that can lead to a progressive failure of the fork, posing a fall hazard.
FDA DevicesEndo-Model Replacement Plateau; Item Number: 15-0027/11;
Endo-Model Replacement Plateau; Item Number: 15-0027/11;
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
FDA FoodMade Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Jalapeno Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA FoodMade Fresh Salads brand Scallion Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Scallion Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA FoodMade Fresh Salads brand Walnut Raisin Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Walnut Raisin Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA FoodMade Fresh Salads brand Strawberry Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Strawberry Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA DevicesPenner Pacific Bathing Spa, Model Numbers 360020-1P
Penner Pacific Bathing Spa, Model Numbers 360020-1P
The device does not bear a unique device identifier.
FDA FoodMade Fresh Salads brand Whipped Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Whipped Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA FoodMade Fresh Salads brand Garlic & Herb Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Garlic & Herb Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA FoodMade Fresh Salads brand Lox Cream Cheese; 5 lb white plastic tub
Made Fresh Salads brand Lox Cream Cheese; 5 lb white plastic tub
Products may be contaminated with Listeria monocytogenes.
FDA DevicesArtelon FlexBand Dynamic Matrix Ref: 31057
Artelon FlexBand Dynamic Matrix Ref: 31057
Augmentation devices failed bacterial endotoxin testing.
FDA DevicesCHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
CHEMISTRY ANALYZER AU5800, REF: B96697, B96698, B23279, B23280, B23281
A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15 minutes may lead to: Reagent Blank and calibration databases not opening errors: CAL History DB Open Error.., RB History DB Open Error..; system will stop analyzing, firm service must visit to apply software solution; may lead to delay in diagnosis and/or patient treatment
FDA DevicesEndo-Model Replacement Plateau; Item Number: 15-8521/15;
Endo-Model Replacement Plateau; Item Number: 15-8521/15;
The potential for an implant with a plateau screw where the bushing could detach from the screw shaft due to a longitudinal fracture.
FDA DevicesGEM Premier 5000; Part No. 00055430008.
GEM Premier 5000; Part No. 00055430008.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.
FDA DevicesGEM Premier 5000; Part No. 00055445004.
GEM Premier 5000; Part No. 00055445004.
Confirmed customer complaints indicating that GEM PAKs (cartridges) for the GEM Premier 5000 may experience an increased incidence of Process Control Solution Not Detected (PCSND) errors during warm-up, including consecutive occurrences, resulting in GEM PAK ejection and requiring insertion of a new GEM PAK. iQM2 is an active quality process control program designed to provide continuous monitoring of the entire testing process. Thus, if a GEM PAK completes AutoPAK Validation following warm-up, it may remain in use. Consecutive GEM PAK ejections during warm-up may prolong turnaround times, potentially delaying results. In such cases, patient management may require reassessment once results are available. While many GEM PAKs continue to perform as intended, consecutive ejections may increase the likelihood of operational disruption, highlighting the importance of advance planning where feasible to help minimize impact.