États-Unis Recalls

Rappels de sécurité de la FDA, CPSC, NHTSA et de l’USDA FSIS.

Showing 24 of 17,563 results
Safety AlertUSCPSC

Rear Bolts on Trek and Electra Electric Bicycles Recalled Due to Fall Hazard; Manufactured by Hyena

Hyena, Inc., of Taiwan
Rear Bolts on Trek and Electra Electric Bicycles Recalled Due to Fall Hazard; Manufactured by Hyena
CPSCGeneral Alert

Rear Bolts on Trek and Electra Electric Bicycles Recalled Due to Fall Hazard; Manufactured by Hyena

The rear wheel bolts can break when torqued, causing the wheel to separate from the bicycle, posing a fall hazard.

Jan 29, 2026Hyena, Inc., of Taiwan
Safety AlertUSCPSC

Northern Tool + Equipment Recalls Hot Water Pressure Washers Due to Fire Hazard

Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
Northern Tool + Equipment Recalls Hot Water Pressure Washers Due to Fire Hazard
CPSCGeneral Alert

Northern Tool + Equipment Recalls Hot Water Pressure Washers Due to Fire Hazard

The fan wheel on the recalled pressure washers can fail, causing abnormal burner operation that can produce smoke and/or bursts of flames during use, posing a fire hazard.

Jan 29, 2026Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
Safety AlertUSCPSC

Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements

Unknown Firm
Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements
CPSCGeneral Alert

Bazic Products Recalls Bazic Silicone Glue Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child Resistant Packaging and FHSA Labeling Requirements

The glue contains methanol, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The glue's packaging is not child-resistant, posing a risk of serious injury or death from poisoning if the contents are swallowed by young children. In addition, the glue violates the labeling requirements under the Federal Hazardous Substances Act because it is incorrectly labeled as "Non-Toxic" and because it lacks a "highly flammable" hazard statement.

Jan 29, 2026
Safety AlertUSCPSC

Primark Recalls The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets Due to Ingestion Hazard

Unknown Firm
Primark Recalls The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets Due to Ingestion Hazard
CPSCGeneral Alert

Primark Recalls The Nightmare Before Christmas Glow-in-the-Dark Coloring Sets Due to Ingestion Hazard

The crayons in the coloring set have high levels of strontium and aluminum, and this may present a risk if ingested, posing a poisoning hazard if ingested by young children.

Jan 29, 2026
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite V5, elite V6, elite V8 Product Description: V series Patient Monitor including elite V5, elite V6 and elite V8 which can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormity so that doctors and nurses can deal with them in time. The V series Patient Monitor realize the monitoring of physiological parameters by configuration with different parameter modules which include SpO2 (pulse oxygen saturation, pulse rate and SpO2 plethysmogram) with EDAN SpO2 module or Nellcor SPO2 module, NIBP (systolic pressure, diastolic pressure, mean pressure and pulse rate), TEMP, ECG, RESP(respiration), CO2, IBP, C.O. and AG(anesthetic gas), RM(respiratory mechanics), BIS(bispectral index) and ICG(impedance cardiography). Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: elite V5, elite V6, elite V8 Product Description: V series Patient Monitor including elite V5, elite V6 and elite V8 which can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormity so that doctors and nurses can deal with them in time. The V series Patient Monitor realize the monitoring of physiological parameters by configuration with different parameter modules which include SpO2 (pulse oxygen saturation, pulse rate and SpO2 plethysmogram) with EDAN SpO2 module or Nellcor SPO2 module, NIBP (systolic pressure, diastolic pressure, mean pressure and pulse rate), TEMP, ECG, RESP(respiration), CO2, IBP, C.O. and AG(anesthetic gas), RM(respiratory mechanics), BIS(bispectral index) and ICG(impedance cardiography). Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Medical DeviceUSFDA Devices

ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), 400021001 (Philippines)

ICU Medical, Inc.
FDA DevicesClass II

ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), 400021001 (Philippines)

Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed.

Jan 28, 2026ICU Medical, Inc.
Food & BeverageUSFDA Food

Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (680g)) packaged in wax paper placed in clear bag and packed in cardboard carton. 12/ 24 oz per master case.

CATAO MARKET LLC
FDA FoodClass II

Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 24 oz (680g)) packaged in wax paper placed in clear bag and packed in cardboard carton. 12/ 24 oz per master case.

Undeclared colors FD&C Yellow #5

Jan 28, 2026CATAO MARKET LLC
Food & BeverageUSFDA Food

Cuban Crackers Galletas Cubanas, Net Wt 8Oz (226g). Distributed by Best Floridian, LLC. UPC 5700300060

Lily's Bakery Factory
FDA FoodClass II

Cuban Crackers Galletas Cubanas, Net Wt 8Oz (226g). Distributed by Best Floridian, LLC. UPC 5700300060

Undeclared colors FD&C yellow #5, FD&C yellow #6, and FD&C red 40

Jan 28, 2026Lily's Bakery Factory
Medical DeviceUSFDA Devices

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

Medline Industries, LP
FDA DevicesClass I

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.

Jan 28, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

ICU Medical Plum Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines)

ICU Medical, Inc.
FDA DevicesClass II

ICU Medical Plum Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines)

Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed.

Jan 28, 2026ICU Medical, Inc.
Food & BeverageUSFDA Food

Anthony's Barbecue & Dip-It Sauce, 15 oz. (425g) glass bottle, UPC 6 89076 62272 1. Anthony's BBQ Sauce PO Box 3239 Harbor, OR 97415. The ingredients statement on the recalled bottle is declared as "***Ingredients: Tomatoes, Brown Sugar, Distilled Water, Distilled Vinegar, Garlic, Onion, Liquid Smoke, Salt, Mustard Seed, Natural Flavor, Corn syrup, Turmeric, Paprika, Pepper, Hydrolyzed soy protein, Caramel color, 1/10 of 1% Benzoate of Soda***.

Anthony's BBQ
FDA FoodClass I

Anthony's Barbecue & Dip-It Sauce, 15 oz. (425g) glass bottle, UPC 6 89076 62272 1. Anthony's BBQ Sauce PO Box 3239 Harbor, OR 97415. The ingredients statement on the recalled bottle is declared as "***Ingredients: Tomatoes, Brown Sugar, Distilled Water, Distilled Vinegar, Garlic, Onion, Liquid Smoke, Salt, Mustard Seed, Natural Flavor, Corn syrup, Turmeric, Paprika, Pepper, Hydrolyzed soy protein, Caramel color, 1/10 of 1% Benzoate of Soda***.

Undeclared allergen (fish). Anthony's Barbecue & Dip-It Sauce label does not declare Worcestershire (Anchovy).

Jan 28, 2026Anthony's BBQ
Medical DeviceUSFDA Devices

RayStation/RayPlan. Model/Catalog Numbers: 12.0.0, 12.1.0, 12.0.3, 12.0.4, 12.3.0. Software Version: RayStation 11B, RayStation 11B SP1, RayStation 11B SP2, RayStation 11B SP3, RayStation 11B SPT1. Radiation Therapy Treatment Planning System

RAYSEARCH LABORATORIES AB
FDA DevicesClass II

RayStation/RayPlan. Model/Catalog Numbers: 12.0.0, 12.1.0, 12.0.3, 12.0.4, 12.3.0. Software Version: RayStation 11B, RayStation 11B SP1, RayStation 11B SP2, RayStation 11B SP3, RayStation 11B SPT1. Radiation Therapy Treatment Planning System

Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.

Jan 28, 2026RAYSEARCH LABORATORIES AB
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3 Product Description: The Vital Signs Monitor is a portable device intended for use by health care professionals. The monitor could provide the monitoring of physiological parameters such as the non-invasive blood pressure (NIBP), the oxygen saturation of the blood (SpO2) and Rectal/Oral/Auxiliary/Ear temperature measurement. Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: M3 Product Description: The Vital Signs Monitor is a portable device intended for use by health care professionals. The monitor could provide the monitoring of physiological parameters such as the non-invasive blood pressure (NIBP), the oxygen saturation of the blood (SpO2) and Rectal/Oral/Auxiliary/Ear temperature measurement. Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Medical DeviceUSFDA Devices

Philips Azurion system; Software Version Number: R3.1;

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
FDA DevicesClass II

Philips Azurion system; Software Version Number: R3.1;

Philips has identified two (2) software issues affecting device systems that may result in loss of imaging (X-ray) functionality and/or loss of motorized movement, and/or incorrect image content and/or loss of data. Issue 1 - System remains in continuous restart mode after the start-up. Issue 2 - Longitudinal Position Error Applicable only to systems with Poly-G3 frontal stand.

Jan 28, 2026PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10, iX12, iX15 Product Description: The iX series Patient Monitors including iX10, iX12, iX15 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormalities so that doctors and nurses can respond to the patient's situation as appropriate. Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iX10, iX12, iX15 Product Description: The iX series Patient Monitors including iX10, iX12, iX15 can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormalities so that doctors and nurses can respond to the patient's situation as appropriate. Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, including non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), and Quick TEMP/Infrared TEMP (TEMP). iM3 capabilities include storing, displaying measuring data. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Vital Signs Monitor Model/Catalog Number: iM3 Product Description: The iM3 has three work modes, Monitor, Spot and Round, to measure physiological parameters, including non-invasive blood pressure (NIBP), oxygen saturation of the blood (SpO2), pulse rate (PR), and Quick TEMP/Infrared TEMP (TEMP). iM3 capabilities include storing, displaying measuring data. When necessary, alarms will be produced so that doctors and nurses can manage patient care appropriately. Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Medical DeviceUSFDA Devices

Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 17.0.0, 17.0.1 Software Version: RayStation v2025, RayStation v2025 SP1 Product Description: Radiation Therapy Treatment Planning System Component: No

RAYSEARCH LABORATORIES AB
FDA DevicesClass II

Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 17.0.0, 17.0.1 Software Version: RayStation v2025, RayStation v2025 SP1 Product Description: Radiation Therapy Treatment Planning System Component: No

Potential for the invalidation for calculated radiation dose does not work as intended for certain Regions of Interest (ROIs). This issue occurs for some ROI(s) which have no contours and either have a material override defined, or are of type Bolus, Fixation, or Support. In these cases, adding geometry to the ROI, subsequently modifying geometry, or removing the material override does not invalidate dose as intended.

Jan 28, 2026RAYSEARCH LABORATORIES AB
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyzing and processing. After that, data will be sent to MFM-CMS via Wi-Fi. The parameters supported are ECG, SpO2 and PR. Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Telemetry Transmitter Model/Catalog Number: iT20 Product Description: iT20 collects physiological parameters by ECG cables and SpO2 sensors, then achieves data analyzing and processing. After that, data will be sent to MFM-CMS via Wi-Fi. The parameters supported are ECG, SpO2 and PR. Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Medical DeviceUSFDA Devices

Patient Information Center iX; Software Version Number: 4.5.0

Philips North America
FDA DevicesClass II

Patient Information Center iX; Software Version Number: 4.5.0

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

Jan 28, 2026Philips North America
Medical DeviceUSFDA Devices

MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.

Medline Industries, LP
FDA DevicesClass I

MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.

Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire. Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.

Jan 28, 2026Medline Industries, LP
Medical DeviceUSFDA Devices

Merit Medical , Custom Manifold Kit REF: K09-13203A

Merit Medical Systems, Inc.
FDA DevicesClass II

Merit Medical , Custom Manifold Kit REF: K09-13203A

Inflation device handle may detach from the syringe during procedure.

Jan 28, 2026Merit Medical Systems, Inc.
Medical DeviceUSFDA Devices

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8, iM8A, iM8B Product Description: iM8 Series Patient Monitor can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormity so that doctors and nurses can deal with them in time. The patient monitor supports software upgrade online and networking and build-in battery power is available for all the models. iM8 Series Patient Monitor can monitor physiological parameters including SpO2, NIBP, ECG, RESP, TEMP, CO2, IBP. The above is the maximum configuration, the user may select different monitoring parameters in according with the requirement. iM8 Series patient monitor includes three models iM8, iM8A, iM8B, and screen size is the primary difference for three models. Component: No

Edan Diagnostics
FDA DevicesClass II

Brand Name: EDAN Product Name: Patient Monitor Model/Catalog Number: iM8, iM8A, iM8B Product Description: iM8 Series Patient Monitor can perform long-time continuous monitoring of multiple physiological parameters. Also, it is capable of storing, displaying, analyzing and controlling measurements, and it will indicate alarms in case of abnormity so that doctors and nurses can deal with them in time. The patient monitor supports software upgrade online and networking and build-in battery power is available for all the models. iM8 Series Patient Monitor can monitor physiological parameters including SpO2, NIBP, ECG, RESP, TEMP, CO2, IBP. The above is the maximum configuration, the user may select different monitoring parameters in according with the requirement. iM8 Series patient monitor includes three models iM8, iM8A, iM8B, and screen size is the primary difference for three models. Component: No

As a result of receiving an FDA It Has Come to Our Attention Letter (IHCTOA Letter) regarding potential cybersecurity issues with various of the firm device.

Jan 28, 2026Edan Diagnostics
Food & BeverageUSFDA Food

All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food

GOLD STAR DISTRIBUTION INC
FDA FoodClass II

All human food products distributed from the firm. Including but not limited to: snack foods, candy, gum, cooking oil, canned fruit and beans, honey, Dietary supplements, peanut butter, oatmeal, rice, dry peas and beans, ramen, cold cereal, hot sauce, lemon juice, crackers, canned sardines tuna and Oyster, sauces, seasonings, sugar, bottled and canned beverages, coffee and filters and creamer, tea bags, canned pasta, dates, flour, baby food

Potential exposure of rodents and rodent activity in the distribution center.

Jan 28, 2026GOLD STAR DISTRIBUTION INC
Medical DeviceUSFDA Devices

Merit Medical , Custom Inflation Kit REF: K05-00761F K05-01717B K05-02080D K05-02090C K05-02221 K05-02338 K05-02470 K05-02954 K05-03094A K05T-00380C K05T-01674B K05T-01863 K05T-01915 K05T-01920F K05T-01955 K05T-02138 K05T-02138A K05T-02272G K05T-02272H K05T-02533 K05T-03153 K05T-03201

Merit Medical Systems, Inc.
FDA DevicesClass II

Merit Medical , Custom Inflation Kit REF: K05-00761F K05-01717B K05-02080D K05-02090C K05-02221 K05-02338 K05-02470 K05-02954 K05-03094A K05T-00380C K05T-01674B K05T-01863 K05T-01915 K05T-01920F K05T-01955 K05T-02138 K05T-02138A K05T-02272G K05T-02272H K05T-02533 K05T-03153 K05T-03201

Inflation device handle may detach from the syringe during procedure.

Jan 28, 2026Merit Medical Systems, Inc.

Install The Recall File App

Check safety warnings, scan your pantry, and monitor your vehicles directly from your home screen.