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.
Start with the product name or brand. If the list is too broad, search the exact UPC, lot code, model number, date code, NHTSA campaign number or official recall number printed on the notice or label.
Results help you find a possible match quickly. Before you stop use, discard, return or repair anything, open the official notice and confirm every affected detail.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
|
Window Glass May Detach from Frame/FMVSS 217
Nova Bus (US) Inc. (Nova Bus) is recalling certain Ricon hidden frame windows sold through Prevost Parts and Prevost Service Center. Please refer to Nova Bus' attached document for specific part number information. Inadequate adhesion around the window frame may cause the glass to detach. As such, these windows fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 217, "Bus Emergency Exits and Window Retention and Release." The glass can fall out of the frame, increasing the risk of ejection and injury during a crash. Detached window glass can also become a road hazard for other vehicles, increasing the risk of a crash.
|
NHTSA
26E019000
|
Vehicle | High |
Apr 9, 2026
Recall: Apr 9, 2026
|
Details |
|
Touch Screen Display May Fail
Weldon Division of Akron Brass (Akron Brass) is recalling certain Enovation Controls PowerView 700 displays with part number 610-00060-080-ST or 610-00060-080. The display may stop responding to touch commands or fail to power on, preventing the activation of exterior emergency lights, fire fighting and other emergency equipment. A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
|
NHTSA
26E020000
|
Vehicle | High |
Apr 9, 2026
Recall: Apr 9, 2026
|
Details |
|
Air Bags May Deploy Unexpectedly
Honda (American Honda Motor Co.) is recalling certain 2018-2022 Odyssey vehicles. A software programming error can cause the side and side curtain air bags to deploy unexpectedly. Air bags that deploy unexpectedly can increase the risk of injury.
|
NHTSA
26V227000
|
Vehicle | Medium |
Apr 9, 2026
Recall: Apr 9, 2026
|
Details |
|
Deactivated Warning Lights & Stop Sign
Daimler Trucks North America, LLC (DTNA) is recalling certain Thomas Built Buses 2024-2027 Saf-T-Liner C2 school buses. The vehicle's software may misinterpret contact if the door switch is bumped, deactivating the amber and red warning lights and the stop sign arm. Warning lights and a stop sign arm that fail to activate will not warn other drivers the school bus is slowing down, increasing the risk of a crash or injury.
|
NHTSA
26V228000
|
Vehicle | High |
Apr 9, 2026
Recall: Apr 9, 2026
|
Details |
|
MEI HEONG YUEN GARLIC FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Garlic, Liquorice, Sugar, Saccharin; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; UPC: 6912449124329
Products contain cyclamates (banned sweetener)
|
FDA
H-0643-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 19, 2026
|
Details |
|
MEI HEONG YUEN WALNUT FLAVOR ROASTED PEANUTS; 9.17 oz (260g); Ingredients: Peanuts, Salt, Liquorice, Sugar, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237; UPC: 6912449124282
Products contain cyclamates (banned sweetener)
|
FDA
H-0642-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 19, 2026
|
Details |
|
Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins, CO 80524.
Product is potentially under-processed.
|
FDA
H-0661-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 24, 2026
|
Details |
|
Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5
The product states wild caught marine collagen and eggshell membrane collagen in ingredient statement but does not state EGG and the specific species of FISH parenthetically or via a Contains statement.
|
FDA
H-0637-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 27, 2026
|
Details |
|
FDA
H-0646-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 30, 2026
|
Details | |
|
MEI HEONG YUEN TANGERINE FLAVOR ROASTED PEANUTS; NET 9.17 oz (260g); Ingredients: Peanuts, Salt, Sugar, Liquorice, Spices, Sodium Cyclamate, Acesulfame-K, Vanilla, Ethyl Maltol; Shelf Life: 18 Months; Manufacturer: Heshan Mei Heong Yuen Food Pte Ltd; Distributor in USA: Super World Trading Inc 28 Varick Ave. Brooklyn, NY 11237 UPC: 6912449124312
Products contain cyclamates (banned sweetener)
|
FDA
H-0641-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 19, 2026
|
Details |
|
Imu-Tek Colostrum-5 120 Capsules; 30% IgG, 2 capsules 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band seal, 500 mg capsule, 7 38654 00026 7, Imu-Tek, Inc. Ft. Collins, CO 80524.
Product is potentially under-processed.
|
FDA
H-0660-2026
|
Food | High |
Apr 8, 2026
Recall: Feb 24, 2026
|
Details |
|
Mama Rose's Prickly Pear Salad Dressing. 12 oz (340 g) glass bottle with gold cap.
Undeclared sulfites.
|
FDA
H-0644-2026
|
Food | High |
Apr 8, 2026
Recall: Nov 5, 2025
|
Details |
|
POPPING BOBA RTD PEACH OOLONG TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
|
FDA
H-0633-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 16, 2026
|
Details |
|
POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
|
FDA
H-0636-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 16, 2026
|
Details |
|
POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
|
FDA
H-0635-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 16, 2026
|
Details |
|
FDA
H-0639-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 5, 2026
|
Details | |
|
POPPING BOBA RTD MIXED BERRY HIBISCUS TEA 12 X 13.8OZ
Packaging integrity issue that may compromise product quality .
|
FDA
H-0634-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 16, 2026
|
Details |
|
" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953
Foreign Object (Glass)
|
FDA
H-0638-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 5, 2026
|
Details |
|
Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
Salmonella spp. identified in finished product testing
|
FDA
H-0640-2026
|
Food | High |
Apr 8, 2026
Recall: Mar 11, 2026
|
Details |
|
Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.
Undeclared milk.
|
FDA
H-0645-2026
|
Food | High |
Apr 8, 2026
Recall: Nov 5, 2025
|
Details |
|
ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1661-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
Cardinal Health Monoject Tuberculin Syringe, 1 mL Luer Lock, Catalog Number 1180100777
The outer packaging and blister pack labeling identify the product as 1mL Luer Lock Tuberculin Syringe (Product Code 1180100777), however the syringes contained within the packages are U-100 Insulin syringes.
|
FDA
Z-1768-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 27, 2026
|
Details |
|
MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death.
|
FDA
Z-1739-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 13, 2026
|
Details |
|
Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
|
FDA
Z-1675-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Mar 3, 2026
|
Details |
|
2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US.
A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread.
|
FDA
Z-1703-2026
|
Medical Device | High |
Apr 8, 2026
Recall: Feb 25, 2026
|
Details |
Use brand, product name, UPC, lot code, best-by date, package size, allergen, contamination issue or distribution state.
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Start broad with the product name, manufacturer, retailer brand or model family. This is usually the fastest way to find a possible notice.
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Use the brand, product name, manufacturer or retailer. If the result list is long, add a code from the label or package.
Read the product description, recall reason, hazard, affected dates, source agency and official recall number before taking action.
Compare the UPC, lot, best-by date, establishment number, model, serial range, color, size, state, retailer and product photo.
The notice may say stop using, do not eat, discard, return for refund, request a repair kit, replace a part or schedule dealer service.
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.
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.
Use campaign results to understand the issue, then verify your VIN, car seat model or tire information with NHTSA or the manufacturer.
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.
A product recall is a safety or compliance notice saying a product may need to be corrected, removed, returned, repaired, replaced, refunded or discarded.
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.
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.
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.
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.
Yes. Lot codes are especially useful for food, drug, cosmetic and pet food recalls because only certain production batches may be affected.
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.
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.