Recall archive
31,892 recalls · page 110 of 1329
Reported Oct 17, 2025
Kenz Henz recalls Kenz Henz Grade AA Large Pasture Raised Eggs due to Potential to be contaminated with Salmonella
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Kenz Henz
FDA (recalls & safety alerts)
Reported Oct 17, 2025
Nat’s Nuts recalls Nat’s Nuts Cinnamon Whiskey Pecans due to Undeclared cashews
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Nat’s Nuts
FDA (recalls & safety alerts)
Reported Oct 17, 2025
Publix recalls Publix Rich & Creamy Vanilla Ice Cream due to May contain undeclared egg allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Publix
FDA (recalls & safety alerts)
Consumer productsReported Oct 16, 2025
Wilteexs Bioethanol Fuel Bottles Recalled Due to Risk of Serious Injury or Death from Flash Fire; Violates Mandatory…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hongyaodekejiyouxiangongsi, dba online seller Wilteexs
CPSC
Consumer productsReported Oct 16, 2025
iFIT Recalls NordicTrack Rowing Machines Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.iFIT Inc.
CPSC
Consumer productsReported Oct 16, 2025
WLIVE Fabric 12-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment; Violates…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jiangsu Pengcheng Weiye Furniture Co., Ltd.
CPSC
Consumer productsReported Oct 16, 2025
RH Recalls Byron Tables and Desks Due to Risk of Injury
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rh US, LLC
CPSC
Consumer productsReported Oct 16, 2025
AOWOS Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shenzhen Shuanglong Home Furnishing Co., Ltd.
CPSC
Consumer productsReported Oct 16, 2025
Belivium Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation and Entrapment Hazards;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shenzhenshiyingjiayueshangmaoyouxiangongsi, dba Belivium
CPSC
Consumer productsReported Oct 16, 2025
Super Wheels (Formerly Allite) Recalls Vaast A/1 Bicycles and Frames Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Super Wheels Inc. f/k/a Allite Inc.
CPSC
Consumer productsReported Oct 16, 2025
Textron E-Z-GO Recalls Personal Transportation Vehicles Due to Risk of Serious Injury and Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Textron E-Z-GO LLC
CPSC
Consumer productsReported Oct 16, 2025
VESTA.DS Recalls VST Brand Tankless Water Heaters Due to Carbon Monoxide (CO) Poisoning Hazard and Risk of Serious…
High riskUsing this product could cause serious injury, illness or death — stop using it now.VESTA.DS, Inc.
CPSC
Consumer productsReported Oct 16, 2025
Yamaha Recalls Model Year 2017-2024 Golf Car Vehicles Due to Risk of Serious Injury or Death from Crash Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yamaha Golf Car Company
1 more product in this recall
CPSC
Reported Oct 15, 2025
Automated Impella Controller (AIC), used for left heart support blood pump, labeled as the following with corresponding…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2025
Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg), 90 Tablets per bottle, Rx Only, Manufactured for Accord…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accord Healthcare, Inc.
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
Doxycycline Hyclate Tablets, USP 100 mg*, 500-count bottle, Rx Only, Distributed by: Acella Pharmaceuticals, LLC,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acella Pharmaceuticals, LLC
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
Wyandotte, Sanifect E3, Hand Sanitizer (Ethanol-Based, Product 5511), Ethyl Alcohol 60.1%, Manufacture By: AFCO, 550…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acuity Specialty Products, Inc.
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Technology Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2025
Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg, 3 Units,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AvKARE
FDA (openFDA drug enforcement)
Reported Oct 15, 2025
PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B Braun Medical Inc.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 15, 2025
SYNCHRON Systems Phosphorus (PHOSm) Reagent REF: 467868 For In Vitro Diagnostic Use, Rx Only.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2025
This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2025
BD Alaris Pump Infusion Sets for the following reference numbers: C24101E, Amber Tubing, 15 Micron Filter, 0.2 Micron…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Oct 15, 2025
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Corneat Vision, Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
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