Product Recall Checker | Search Product Recalls by UPC, Lot Code, Brand or Model

Latest Product Recall Matches

Showing 3,051 - 3,075 of 3,318 matching product recalls.

Product Recall	Source	Type	Risk	Date	Action
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.	FDA Z-1109-2026	Medical Device	High	Jan 28, 2026 Recall: Nov 28, 2025	Details
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.	FDA Z-1108-2026	Medical Device	High	Jan 28, 2026 Recall: Nov 28, 2025	Details
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.	FDA Z-1142-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
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.	FDA Z-1113-2026	Medical Device	High	Jan 28, 2026 Recall: Dec 12, 2025	Details
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.	FDA Z-1140-2026	Medical Device	High	Jan 28, 2026 Recall: Oct 24, 2025	Details
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	Details
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	Details
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	FDA H-0413-2026	Food	High	Jan 28, 2026 Recall: Dec 18, 2025	Details
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	Details
Mini Gaceniga Authentic Cuban Loaf Cake Raisins (Net Wt. 12 oz (340g)) packaged in wax paper, placed in clear bag and packed in cardboard carton. 12/ 12 oz per master case. Undeclared colors FD&C Yellow #5	FDA H-0414-2026	Food	High	Jan 28, 2026 Recall: Dec 18, 2025	Details
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).	FDA H-0407-2026	Food	High	Jan 28, 2026 Recall: Nov 7, 2025	Details
Gacen¿iga Authentic Cuban Loaf Cake Classic (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	FDA H-0412-2026	Food	High	Jan 28, 2026 Recall: Dec 18, 2025	Details
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
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
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.	FDA H-0411-2026	Food	High	Jan 28, 2026 Recall: Dec 26, 2025	Details
Mini Gaceniga Authentic Cuban Loaf Cake Classic (Net Wt. 12 oz (340g)) packaged in wax paper, placed in clear bag and packed in cardboard carton. 12/ 12 oz per master case. Undeclared colors FD&C Yellow #5	FDA H-0415-2026	Food	High	Jan 28, 2026 Recall: Dec 18, 2025	Details
Gregory's Foods Bag Full of Cookies, White Chocolate Macadamia Nut, frozen cookie dough. Net Wt 2 lbs 8.5 oz (1148g). UPC 8 30825-00124 7. Keep Frozen. Gregory's Foods, Inc., 1301 Trapp Road, Eagan, MN 55121. Undeclared peanuts.	FDA H-0409-2026	Food	High	Jan 28, 2026 Recall: Dec 19, 2025	Details
White Castle Original Sliders, Net Wt. 6.35 oz. (180g), packaged as a 4-count carton, each containing 2-Two Packs. UPC 082988029693, packed 6 cartons per case. Undeclared allergens (milk and soy).	FDA H-0416-2026	Food	High	Jan 28, 2026 Recall: Dec 10, 2025	Details
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.	NHTSA 26V048000	Vehicle	High	Jan 28, 2026 Recall: Jan 28, 2026	Details
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.	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.	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.	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.	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.	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

Showing 3,051 - 3,075 of 3,318 product recalls

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Food safety

Food Product Recall Search

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Vehicle Recall Lookup

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Family safety

Baby Product Recall Alerts

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Fresh updates

Latest Product Recalls Today

Browse new and recently updated notices across consumer products, foods, vehicles, medical devices and household items.

What To Enter In The Search Box

A recall usually applies to specific products, batches, model ranges or dates. Use the details printed on the item, package, label, receipt or vehicle paperwork.

Product Name Or Brand

Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.

UPC, Lot Code And Dates

For food, drugs, cosmetics and packaged goods, compare the UPC, lot code, product code, best-by date, use-by date and package size.

Model, Serial Or Date Code

For appliances, electronics, toys, furniture and baby products, match the model number, serial range, date code, color, size and retailer listing.

VIN Or NHTSA Campaign

This site can find vehicle recall campaigns. For your exact car, use the official NHTSA VIN lookup to confirm unrepaired recall status.

Official Sources This Checker Organizes

The goal is to make official notices easier to search. The final decision should still come from the linked agency or manufacturer notice.

CPSC

Consumer Product Recalls

Consumer products, toys, furniture, appliances, electronics and baby products. CPSC remedy details can change after a notice is first posted.

FDA

Food And Medical Device Recalls

FDA-regulated foods, drugs, cosmetics and medical devices. FDA notes that not every recall has a press release on the public recalls page.

USDA FSIS

Meat, Poultry And Egg Product Recalls

Meat, poultry and egg product recalls and public health alerts. Check establishment numbers, lot codes, labels and affected states.

NHTSA

Vehicle, Tire And Car Seat Recalls

Vehicle, tire, equipment and child-seat campaigns. VIN or license plate lookup is needed to know whether your specific vehicle still needs repair.

How To Confirm A Recall Match

1. Search The Obvious Name First

Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.

2. Open The Closest Result

Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.

3. Match Every Identifier

Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.

4. Follow The Official Remedy

The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.

When A Recall Result Looks Like Your Product

Use this checklist before you throw away a product, call the company, request a refund or schedule a repair.

If It Is Food, Formula Or Pet Food

Do not rely on brand alone. Match the package size, UPC, lot code, best-by date, use-by date, distribution states and any allergy or contamination warning.

If It Is A Baby Or Household Product

Look for model number, date code, serial range, color, size, online listing, product photo and the exact hazard such as choking, suffocation, fire or fall risk.

If It Is A Vehicle Or Car Seat

Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.

If The Details Do Not Match

Your item may not be part of that specific recall. Check spelling, older notices, retailer alerts and the official source before deciding it is safe.

What Is A Product Recall?

A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.

What Should You Do After Finding A Recall?

If all affected details match, follow the official instructions. Keep packaging, take photos, save receipts and contact the company or retailer when a refund or repair is offered.

Why Recall Details Must Match Exactly

A similar brand or product name is not enough. UPCs, lot codes, dates, model numbers, serial ranges and distribution areas determine whether your item is included.

How To Avoid Fake Recall Notices

Be careful with text messages, social posts or refund forms that ask for private information. Verify the notice through an official agency, retailer or manufacturer page.

Product Recall FAQ

Short answers for common product recall searches.

Can I search product recalls by UPC code?

Yes, when the official recall notice includes a UPC or product code. If no result appears, also search the brand, product name, package size, lot code and company name.

Can I search product recalls by lot code?

Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.

Does this replace a VIN recall lookup?

No. This tool helps find vehicle recall campaigns and NHTSA numbers. Use the official NHTSA VIN or license plate lookup for vehicle-specific unrepaired recall status.

Are all recalls listed here?

The database combines multiple official U.S. sources, but agencies and companies can publish or update notices at different times. Always check the linked official notice before taking final action.

Product Recall Checker: Search Recalls by UPC, Lot Code, Brand or Model

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