Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,025 found- Lower riskFood
Champion Foods, LLC recalls Motor City Pizza Co. 5 Cheese Bread Single retail pack; 22.43 oz. (1 lb. 6.4 oz.) 636g UPC 8 70375 00511 1; 6 retail
Champion Foods recalls 5 Cheese Bread Singles and Twins with potential salmonella contamination. Consumers should check UPC 8 70375 00511 1 and 8 70375 00509 8 for affected products.
Champion FoodsMay 29, 2026 - Use cautionMedical device
SEASPINE ORTHOPEDICS CORPORATION recalls SeaSpine Polyaxial Head REF Number: 41-3010
SeaSpine recalls polyaxial heads with REF 41-3010 due to potential pop-off during surgery. Affected lots include AW199682G and AW199684G. Contact for replacement.
SeaSpineMay 28, 2026 - Use cautionVehicle
SUBARU FORESTER (2026) recall — Visibility
Subaru recalls 2026 Forester models with potentially detachable moonroof glass, which could become a road hazard and increase crash risk. Owners must have their glass panel inspected by dealers.
SubaruMay 28, 2026 - Use cautionMedical device
Acumed LLC recalls Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL
Acumed recalls specific hexalob screw sizes used in wrist fixation systems due to manufacturing errors that may cause screws to break during use. Affected products include 2.7mm and 3.0mm hexalobe screws with reference numbers listed.
AcumedMay 28, 2026 - UnratedMedical device
Medline Industries, LP recalls Medline Convenience Kits: 1) ANESTHESIA KIT PEDS 90-LF, Model Number: DYNJAP10125A
Medline recalls specific convenience kits containing temperature probes with a distribution error. Affected kits may have safety risks; contact Medline for details.
MedlineMay 28, 2026 - Use cautionMedical device
Medline Industries, LP recalls Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG
Medline recalls convenience kits with Swan-Ganz catheters that may leak or break, risking infection or blood loss. Affected kits include Germantown and University CABG models.
MedlineMay 28, 2026 - UnratedDrug
Ajanta Pharma USA Inc recalls Fenofibrate Capsules, USP 200 mg, Rx only, 100 Capsules, Manufactured by: Ajanta Pharma Limited, India, Marketed by:
Ajanta Pharma USA recalls 200mg Fenofibrate capsules due to CGMP deviations. Consumers should check NDC 27241-120-04 and lot # PA02216 for affected units.
Ajanta PharmaMay 28, 2026 - Use cautionDrug
CareFusion 213, LLC recalls BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) and 70% v/v isopropyl alcohol (IPA) 1 mL Applicator, 60
BD recalls 60 ChloraPrep Clear 1mL applicators due to potential contamination from paper lidding wrinkles breaching the sterile seal. Affected lots have specific expiration dates and are sold by CareFusion 213, LLC.
BDMay 28, 2026 - Use cautionDrug
Guardian Drug Co. Inc. recalls HALEON CALCIUM CARBONATE TUMS ANTACID, Assorted Fruit Tablets, 1000 mg, 160-count bottle, Haleon, Warren, NJ 07059, UPC
Haleon recalls 160-count Tums Antacid tablets due to small metallic particles in chewable tablets. Affected lots expire 1/31/2029. Consumers should check lot numbers on the bottle.
HaleonMay 28, 2026 - Lower riskFood
Azuma Foods International Inc USA recalls azuma foods TAKO WASABI Seasoned Octopus with Wasabi PERISHABLE/KEEP FROZEN PRODUCT OF JAPAN DISTRIBUTED BY: AZUMA
Azuma Foods recalls TAKO WASABI Seasoned Octopus with Wasabi due to undeclared fish content. Products distributed in the US from Japan require immediate attention to avoid potential health risks.
Azuma FoodsMay 28, 2026 - Stop using nowFood
Specialty Bakers, LLC recalls Vanilla Dessert Shells (Giant), 6 dessert shells/1 package, 1 dessert shell is approximately 23.67 grams. 1package is
Specialty Bakers, LLC is recalling Frozen Vanilla Dessert Shells (Giant) because they contain an undeclared allergen: soy. Check your freezer.
Specialty BakersMay 28, 2026 - Use cautionFood
Wise Foods Inc recalls Wise Onion Rings, 3.75 oz, metalized film in cardboard cartons, 14 bags per case,
Wise Foods is recalling 3.75 oz Onion Rings due to undeclared Yellow 5, 6, Blue 1, and unapproved Red 3 dyes. Check your lot codes.
Wise FoodsMay 28, 2026 - Stop using nowConsumer product
Walmart Recalls Mainstays 9-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units
Walmart recalls Mainstays 9-Drawer Fabric Dressers due to tip-over and entrapment hazards that can cause serious injury or death, especially for children. Unanchored dressers violate safety standards.
MainstaysMay 28, 2026 - Stop using nowConsumer product
Tzumi Electronics Recalls SLF Sauna Blankets Due to Fire and Burn Hazards
Tzumi Electronics recalls SLF Sauna Blankets (model 30065TAR) due to fire and burn risks from overheating. Stop using immediately and contact for replacement.
Tzumi ElectronicsMay 28, 2026 - Stop using nowConsumer product
Missry Associates Recalls Misco Sports Light-Up Racket Sets Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
Missry recalls Misco Sports Light-Up Racket Sets (model MT2287) due to button cell batteries being accessible to children, risking serious injury or death if swallowed.
MissryMay 28, 2026 - Stop using nowConsumer product
MiniWarGaming and Primal Horizon Disc Magnets Recalled Due to Risk of Serious Injury or Death from Ingestion; Violate Mandatory Standard for Magnets; Imported by MiniWarGaming
MiniWarGaming disc magnets violate safety standards due to small size and high strength, posing serious ingestion risk to children. Recalled products include specific sizes and packaging. Consumers must stop use and return for refund.
MiniWarGamingMay 28, 2026 - Stop using nowConsumer product
Luminous Fidget Spinner Balls Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Anzmtosn
Anzmtosn's Luminous Fidget Spinner Balls (model FS0862) are recalled due to button cell batteries that can cause serious injury or death if swallowed by children. Consumers must stop using and dispose of batteries safely.
AnzmtosnMay 28, 2026 - Stop using nowConsumer product
Lithium Coin Batteries Recalled Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Coin Batteries; Imported by Proudly American Store, of Canada
Panasonic VL2020 lithium coin batteries sold without child-resistant packaging and required labels are being recalled due to risk of serious injury if swallowed. Consumers should stop using and dispose of batteries safely.
PanasonicMay 28, 2026 - Stop using nowConsumer product
Joy Furniture Recalls Talan and Royce Living Room Furniture Sets Due to Risk of Serious Injury from a Fire Hazard
Joy Furniture recalls Talan and Royce living room sets with faulty power switches that can overheat and cause fire. Consumers must stop using the sets and get a free upgraded switch replacement.
Joy FurnitureMay 28, 2026 - Stop using nowConsumer product
Giantex Recalls Lounge Chairs Due to Amputation Hazard
Giantex recalls blue outdoor lounge chairs (NP10025NY) due to amputation risk. Stop using immediately and contact Giantex for a full refund or destruction instructions.
GiantexMay 28, 2026 - Stop using nowConsumer product
Giantex Recalls Giantex and Costway Portable Steam Saunas Due to Burn Hazard
Giantex recalls portable steam saunas with burn hazard if steam diffuser is too close to body. Consumers must stop using and destroy the sauna by cutting the cord.
GiantexMay 28, 2026 - Stop using nowConsumer product
Daoen Recalls Zen Magnetic Promotional Ball Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys
Daoen recalls Zen-branded magnetic ball fidget toys due to serious injury or death risk from magnet ingestion. Stop using immediately.
ZenMay 28, 2026 - Use cautionVehicle
TIFFIN GT1 (2025) recall — Fuel System, Diesel
Tiffin recalls 2025-2026 GT1 motorhomes for potential fuel leaks that could cause fire if near ignition sources. Owners must park away from structures until repairs are done.
TiffinMay 27, 2026 - Use cautionVehicle
TIFFIN OPEN TRAIL (2026) recall — Equipment
Tiffin recalls 2026-2027 Open Trail RVs with incorrect white CCC label that may cause crash due to misread tire pressure info. Owners must contact Tiffin for free label replacement.
TiffinMay 27, 2026 - Stop using nowVehicle
FORD EXPLORER (2025) recall — Engine And Engine Cooling
Ford recalls certain 2025-2026 Explorers due to engine failure risk. Dealers will replace the engine long block free of charge. Check your VIN for details.
FordMay 27, 2026 - Use cautionVehicle
TOYOTA LAND CRUISER HYBRID (2024) recall — Electrical System
2024 Toyota Land Cruiser Hybrid recall due to instrument panel display failure. Free OTA software update available. Check your VIN for details.
ToyotaMay 27, 2026 - Use cautionVehicle
FORD BRONCO SPORT (2026) recall — Suspension
Ford is recalling 2026 Bronco Sport vehicles with a potential detached control arm that could cause loss of vehicle control and crash risk. Owners must stop driving until repairs are completed.
FordMay 27, 2026 - Use cautionVehicle
FORD EXPEDITION (2020) recall — Seat Belts
Ford is recalling 2020 Expedition vehicles with seat belts that may lock, preventing proper retraction or extension during crashes. Owners must have seat belt retractors inspected and replaced by dealers.
FordMay 27, 2026 - Lower riskMedical device
Inter-Med Llc recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
Inter-Med recalls Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit (Catalog 504600-28) due to incorrect package insert that may instruct users to induce vomiting after ingestion, which is unsafe. Affected units contain Ferric Sulfate Gel instructions instead of proper Aluminum Chloride instructions.
Inter-MedMay 27, 2026 - Use cautionMedical device
Medtronic MiniMed, Inc. recalls MiniMed 780G Insulin Pump, REF: MMT-1885, MMT-1886, MMT-1895, MMT-1896
Medtronic recalls MiniMed 780G insulin pumps with specific software versions due to a software anomaly that can cause insulin delivery to stop when paired with Instinct sensors, risking hyperglycemia or diabetic ketoacidosis.
MedtronicMay 27, 2026
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83,613 recalls tracked · 72,041 explained in plain English · 10,977 manufacturers. Pulled directly from CPSC, FDA, USDA FSIS and NHTSA and refreshed every day.