Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 16.0.0 Software Version: RayStation 2024B 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.
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FDA
Z-1109-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Nov 28, 2025
|
Details |
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Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 15.2.0, 15.1.3 Software Version: RayStation 2024A SP1, RayStation 2024A SP2 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.
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FDA
Z-1108-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Nov 28, 2025
|
Details |
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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.
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FDA
Z-1142-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Oct 24, 2025
|
Details |
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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.
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FDA
Z-1113-2026
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Medical Device | High |
Jan 28, 2026
Recall: Dec 12, 2025
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Details |
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Brand Name: EDAN Product Name: Fetal Monitor Model/Catalog Number: F2, F3 Product Description: The devices are bedside fetal and maternal monitors, which are used to monitor the physiological parameters of pregnant women including the fetus from 28 weeks gestation. The devices may be used antepartum as well as during labor and delivery. 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.
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FDA
Z-1140-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Oct 24, 2025
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Details |
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Brand Name: RayStation Product Name: RayStation/RayPlan Model/Catalog Number: 14.0.0, 15.0.0, 15.1.3 Software Version: RayStation 2023B, RayStation 2024A, RayStation 2024A SP3 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.
|
FDA
Z-1106-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Nov 28, 2025
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Details |
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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.
|
FDA
Z-1110-2026
|
Medical Device | High |
Jan 28, 2026
Recall: Nov 28, 2025
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Details |
|
FDA
H-0413-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 18, 2025
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Details | |
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MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MADE WITH PRIDE AND CARE FOR H-E-B-, SAN ANTONIO, TEXAS 78204
Undeclared Milk. Wrong product in container.
|
FDA
H-0457-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 8, 2025
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Details |
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FDA
H-0414-2026
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Food | High |
Jan 28, 2026
Recall: Dec 18, 2025
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Details | |
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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).
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FDA
H-0407-2026
|
Food | High |
Jan 28, 2026
Recall: Nov 7, 2025
|
Details |
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FDA
H-0412-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 18, 2025
|
Details | |
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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
|
FDA
H-0458-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 2, 2025
|
Details |
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Australian Greenlip Abalone, Frozen, 9 pieces, Net Wt. 23.5 OZ UPC: 9335533013342
Potential Listeria Monocytogenes contamination
|
FDA
H-0406-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 24, 2025
|
Details |
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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.
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FDA
H-0411-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 26, 2025
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Details |
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FDA
H-0415-2026
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Food | High |
Jan 28, 2026
Recall: Dec 18, 2025
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Details | |
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FDA
H-0409-2026
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Food | High |
Jan 28, 2026
Recall: Dec 19, 2025
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Details | |
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FDA
H-0416-2026
|
Food | High |
Jan 28, 2026
Recall: Dec 10, 2025
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Details | |
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Damaged Brake Hose May Leak
Zero Motorcycles Inc. (Zero) is recalling certain 2024-2025 DSR/X, DS, DSR, and DSRP motorcycles. The front brake hose may be twisted and become damaged, which can cause a brake fluid leak and a loss of brake pressure. A loss of brake pressure can reduce braking ability and cause a loss of vehicle control, increasing the risk of a crash.
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NHTSA
26V048000
|
Vehicle | High |
Jan 28, 2026
Recall: Jan 28, 2026
|
Details |
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Unlocked Rear Door May Open Unexpectedly
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023-2024 Prius Prime, 2023-2026 Prius, and 2025-2026 Prius Plug-in Hybrid vehicles. Water may enter the rear door switch and cause a short circuit, allowing an unlocked rear door to open unexpectedly. A door that unexpectedly opens while the vehicle is moving increases the risk of injury.
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NHTSA
26V049000
|
Vehicle | Medium |
Jan 28, 2026
Recall: Jan 28, 2026
|
Details |
|
Loss of Rear Brakes
Ducati North America (Ducati) is recalling certain 2025-2026 Streetfighter V4, Streetfighter V4 S, Panigale V4, and Panigale V4 S motorcycles. Excessive heat may damage the rear brake hose between the ABS control unit and brake caliper, resulting in a sudden loss of the rear brakes. A sudden loss of rear brake function increases the risk of a crash or injury.
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NHTSA
26V050000
|
Vehicle | High |
Jan 28, 2026
Recall: Jan 28, 2026
|
Details |
|
Instrument Panel Display Failure/FMVSS 101, 138
Kia America, Inc. (Kia) is recalling certain 2025 Kia K4, 2025-2026 Sorento, Sorento Hybrid, Sorento Plug-In Hybrid Electric (PHEV), 2026 Sportage, Sportage Hybrid, Sportage PHEV, K5, EV9, Carnival, and Carnival Hybrid vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 101, "Controls and Displays" and 138, "Tire Pressure Monitoring System." An instrument panel display that fails to show critical safety information, such as the speedometer, tire pressure, or warning lights, increases the risk of a crash.
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NHTSA
26V046000
|
Vehicle | High |
Jan 27, 2026
Recall: Jan 27, 2026
|
Details |
|
Instrument Panel Display Failure/FMVSS 101
Hyundai Motor America (Hyundai) is recalling certain 2025-2026 Tucson Hybrid, Tucson Plug-In Hybrid Electric (PHEV), 2026 IONIQ 5, Santa Cruz, Kona, Palisade, Palisade Hybrid, Santa Fe, Santa Fe Hybrid, Sonata, Sonata Hybrid, and Tucson vehicles. Due to a software error, the instrument panel display may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
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NHTSA
26V047000
|
Vehicle | High |
Jan 27, 2026
Recall: Jan 27, 2026
|
Details |
|
U-Bolt May Loosen and Shift Axle
Grand Design RV, LLC (Grand Design) is recalling certain 2021-2024 Momentum and 2022-2024 Solitude Fifth Wheel trailers. The U-bolt may become loose due to inadequate preload and preload losses, causing the axle to move out of position. An axle that moves out of position can cause a loss of vehicle control and increase the risk of a crash.
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NHTSA
26V044000
|
Vehicle | High |
Jan 26, 2026
Recall: Jan 26, 2026
|
Details |
|
Murphy Bed May Fall Unexpectedly
Keystone RV Company (Keystone) is recalling certain 2026 Coleman travel trailers. The bed brackets may not be secured to a stud, causing the bed to fall unexpectedly. A murphy bed that falls increases the risk of injury.
|
NHTSA
26V045000
|
Vehicle | Medium |
Jan 26, 2026
Recall: Jan 26, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.