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Latest recalls
35,021 found- Stop using nowVehicle
TIFFIN WAYFARER (2026) recall — Equipment
Tiffin recalls certain 2026-2027 Wayfarer RVs due to LP tanks that may not shut off or detach, creating fire and crash hazards. Free dealer repair available.
TiffinAug 31, 2026 - Use cautionFood
LMSI, LLC recalls Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17
LMSI, LLC recalls Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil because it contains garlic essential oil not approved for culinary use.
KofinasAug 29, 2026 - Use cautionMedical device
LeMaitre Vascular, Inc. recalls TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;
LeMaitre Vascular recalls 54 units of TufTex Over-the-Wire Embolectomy Catheter (Catalog E1651-88) due to potential balloon failure during medical procedures. Affected units distributed nationwide in specific states.
LeMaitre VascularAug 28, 2026 - Use cautionMedical device
Intellijoint Surgical, Inc. recalls Intellijoint Navigation System: Workstation G2 Configured, REF: 000-0241; Intellijoint HIP Cart System, REF: 000-0250;
Intellijoint Navigation System Workstation G2 (REF: 000-0241) may overheat due to Apple battery recall, posing fire risk. Affected units include specific REF and MacBook serial numbers. Contact manufacturer for remedy.
IntellijointAug 28, 2026 - Lower riskMedical device
Philips North America recalls Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T
Philips recalls Ingenia 3.0T and 3.0T CX MRI scanners with model numbers 781342, 781377, 782103, and 781271 due to incorrect diffusion tensor imaging data exports that may cause inaccurate nerve pathway mapping in brain imaging software.
PhilipsAug 28, 2026 - Lower riskDrug
Amneal Pharmaceuticals of New York, LLC recalls Exenatide Injection, USP, 250 mcg/mL, 1.2 mL per prefilled pen, Rx Only, Subcutaneous Use Only, For Single Patient Use
Amneal recalls Exenatide injection pens that may contain no medication. This could lead to ineffective diabetes treatment. Check your pen's lot number and contact Amneal for details.
AmnealAug 28, 2026 - Use cautionPet food
Northwest Naturals – Chicken Recipe: Potential contamination with Salmonella and/or Listeria monocytogenes
Northwest Naturals is recalling chicken recipe pet food due to potential Salmonella and Listeria monocytogenes contamination. Consumers should stop feeding affected products and return unused portions for full refunds.
Northwest NaturalsAug 28, 2026 - Stop using nowFood
Frutas y Hortalizas del Sur S.A. recalls Organic Triple Berry Blend Strawberries, Blackberries & Blueberries, NET WT 10 OZ (283g), packed in plastic bag, 5 bags
Organic Triple Berry Blend strawberries recalled due to potential E. coli O145:H28 contamination. Consumers should stop using if they have the product with lot number 6 040 01-6.
Frutas y Hortalizas del SurAug 28, 2026 - UnratedFood
Tiffany Food Corp recalls Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.;
Tiffany Food Corp recalls Hexing Haw Balls candy due to unapproved dye Ponceau 4R. Products packaged in 200g clear plastic bags with best before 10/01/2026.
Tiffany Food CorpAug 28, 2026 - Lower riskMedical device
Merit Medical Systems, Inc. recalls Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT
Merit Medical Systems recalls Scout MD Delivery System (MDS05A-01, MDS05C-01, MDS10C-01) due to potential clip deployment failures affecting surgical guidance.
Merit Medical SystemsAug 27, 2026 - Lower riskMedical device
Olympus Corporation of the Americas recalls Olympus Tripp-Lite P580-025 25ft DisplayPort Cable, Model Number P580-025, an accessory used in conjunction wtih
Olympus recalls 543 P580-025 DisplayPort cables sold worldwide for possible video dropout during high-power operation. Affected cables were sold in the US and Poland. Return or stop using immediately.
OlympusAug 27, 2026 - Lower riskDrug
Macleods Pharmaceuticals Limited recalls Olanzapine Tablets, USP 5 mg, 30-count bottle, Rx Only, Manufactured For: Macleods Pharma USA, Inc. Princeton, NJ,
Macleods Pharmaceuticals recalls 5mg Olanzapine tablets due to impurities that could pose health risks. Affected products have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
MacleodsAug 27, 2026 - Stop using nowConsumer product
Montessori Baby Toy Sets Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by Chillife Official
Chillife 5-in-1 Montessori Baby Toy Sets with small silicone strings that can cause choking are recalled. Consumers must stop using, destroy toys by cutting strings and marking as destroyed, then dispose of them.
ChillifeAug 27, 2026 - Stop using nowConsumer product
Kmaier Recalls Infant Walkers Due to Risk of Serious Injury or Death from Fall Hazard; Violate Mandatory Standard for Infant Walkers
Kmaier recalls infant walkers due to fall hazards. Stop using immediately, destroy the unit, and contact Kmaier for a full refund.
KmaierAug 27, 2026 - Stop using nowConsumer product
HABA USA Recalls Rainbow Rattle Grasping and Teething Toys Due to Risk of Serious Injury or Death from Choking and Ingestion Hazards
HABA USA recalls Rainbow Rattle Grasping and Teething Toys due to choking risks. Stop using immediately, destroy the toy, and contact HABA for a full refund.
HABAAug 27, 2026 - Stop using nowConsumer product
Walmart Reannounces Recall of Mainstays Nine-Drawer Fabric Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Walmart Distributed Recalled Dressers Post-Recall; Sold to Consumers Through Liquidators
Walmart recalls Mainstays 9-Drawer Fabric Dressers (2023-2025) due to tip-over and entrapment hazards that can cause serious injury or death to children. Unanchored dressers pose risks.
MainstaysAug 27, 2026 - Stop using nowConsumer product
Steelite Pressure Washers Recalled Due to Risk of Serious Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by Longer 3D
Steelite electric pressure washers without GFCI protection and adequate power cord recalled due to electrocution risk. Consumers must stop using and destroy units by cutting cord in half.
SteeliteAug 27, 2026 - Stop using nowConsumer product
Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards; Sold on Amazon by YERYORK
YERY: 300 units of pressure washers without GFCI pose electrocution risk. Stop using immediately and return for refund.
YERYORKAug 27, 2026 - Stop using nowConsumer product
Little Loves & Co. Recalls Youth Clothing with Drawstrings Due to Risk of Serious Injury or Death from Entrapment Hazard
Little Loves & Co. recalls youth clothing with drawstrings that can cause entrapment injuries or death. Consumers should stop using and return items for refund or cut drawstrings.
Little Loves & Co.Aug 27, 2026 - Stop using nowConsumer product
Excel Industries Recalls Accessory LED Light Kits Due to Risk of Serious Injury from Fire Hazard
Excel Industries recalls accessory LED light kits for Hustler and BigDog mowers due to fire hazard from overheating. Consumers must stop using immediately and get refunds by returning kits to dealers.
Excel IndustriesAug 27, 2026 - Use cautionConsumer product
Diamond Wipes International Recalls MD Wipe Outz Numbing Tattoo Wipes Due to Risk of Serious Injury or Death from Child Poisoning; Violate Mandatory Standard for Child-Resistant Packaging
Diamond Wipes recalls MD Wipe Outz Numbing Tattoo Wipes due to child poisoning risk from non-child-resistant packaging. Consumers must secure wipes away from children and get a refund.
Diamond WipesAug 27, 2026 - Stop using nowConsumer product
Conair Expands Recall of Cuisinart Grill Brushes Due to Ingestion Hazard; Over 3.6 Million Brushes Now Recalled
Conair recalls over 3.6 million metal wire grill brushes due to small metal bristles detaching and posing ingestion hazards that could cause serious internal injuries requiring surgery.
ConairAug 27, 2026 - Stop using nowConsumer product
AudioLineOut Recalls Studio Six Headphone Amplifiers Due to Risk of Serious Injury or Death from Electrocution Hazard
AudioLineOut recalls Studio Six Headphone Amplifiers with model ST6 due to electrocution risk when used with aftermarket metal base tubes. Consumers must stop using immediately and return for free repair.
AudioLineOutAug 27, 2026 - Use cautionMedical device
Canon Medical System, USA, INC. recalls Alphenix INFX-8000C/B5
Canon Medical recalls one Alphenix INFX-8000C/B5 device (serial B5F2532011/UDI 4987670100192) due to risk of tabletop shifting causing imaging errors. Stop using immediately.
Canon MedicalAug 26, 2026 - Use cautionMedical device
GRI Medical & Electronic Technology Co., Ltd. recalls HALYARD Laparoscopy Comprehensive Pack II REF: 49332
GRI Medical recalls 396 laparoscopy packs labeled 'latex free' that contain a latex urethral catheter. Affected kits sold in Mississippi with specific lot numbers. Stop using immediately.
GRI MedicalAug 26, 2026 - Use cautionMeat & poultry
Shanghai Ravioli Corporation Recalls Not Ready-To-Eat Frozen Buffalo Chicken Products Produced Without the Benefit of Inspection
USDA FSIS recalls ~24,900 lbs of frozen Buffalo chicken products made without inspection due to potential allergens and contaminants. Products should be thrown away or returned to purchase location.
Shanghai Ravioli CorporationAug 26, 2026 - Stop using nowPet food
Shelter’s Choice, Breeder’s Edge – Feline Milk Replacers: Low levels of potassium, copper, folic acid, choline and/or pyridoxine (vitamin B6)
Revival Animal Health recalls Shelter's Choice and Breeder's Edge feline milk replacers due to low potassium, copper, and vitamin B6 levels that can cause fatal or permanent damage in kittens.
Shelter's ChoiceAug 26, 2026 - Stop using nowFood
FOODS ALIVE INC. recalls Foods Alive organic moringa leaf powder, 8oz pouch, UPC 8 91551 00092 8
Foods Alive is recalling 8oz pouches of organic moringa leaf powder due to potential Salmonella contamination. Check your UPC and lot code.
Foods AliveAug 26, 2026 - Lower riskDrug
Mylan Pharmaceuticals Inc recalls Carton label: Mycophenolate Mofetil for injection, USP, 500 mg/vial, Sterile, 4 Single Dose Vials, Rx only,
Mylan recalls 500mg Mycophenolate Mofetil injections due to failed dissolution specifications. Affected lots manufactured in India with specific NDC numbers and expiration dates. Patients should contact Mylan for details.
MylanAug 26, 2026 - Use cautionVehicle
MITSUBISHI OUTLANDER (2025) recall — Back Over Prevention
Mitsubishi recalls 2025-2026 Outlander and PHEV models due to rearview camera software failure causing reduced driver visibility. Owners must update A-IVI software by September 2026 to prevent crashes.
MitsubishiAug 26, 2026
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