Recall archive
31,892 recalls · page 231 of 1329
Reported Jul 26, 2024
Supreme Service Solutions LLC recalls Supreme Produce Vegetable products due to Potential Foodborne Illness – Listeria monocytogenes
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Supreme Service Solutions LLC
FDA (recalls & safety alerts)
Consumer productsReported Jul 25, 2024
Clark Associates Recalls Lancaster Table & Seating Plastic Restaurant High Chairs Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Clark Core Services LLC, d/b/a Clark Associates
CPSC
Consumer productsReported Jul 25, 2024
DGL Group Recalls Hover-1 Dynamo E-Scooters Due to Risk of Serious Injury and Crash Hazard; Sold Exclusively at…
High riskUsing this product could cause serious injury, illness or death — stop using it now.DGL Group Ltd.
CPSC
Consumer productsReported Jul 25, 2024
Grand Rapids Chair Company Recalls Wood Dining Chairs Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grand Rapids Chair Company
CPSC
Consumer productsReported Jul 25, 2024
iFIT Recalls ProForm 50 LB Adjustable Dumbbells Due to Impact Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.iFIT Inc., f/k/a Icon Health & Fitness
CPSC
Consumer productsReported Jul 25, 2024
Kawasaki USA Recalls Mule PRO 1000 Off-Highway Utility Vehicles Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kawasaki Motors Manufacturing Corp., U.S.A.
CPSC
Consumer productsReported Jul 25, 2024
Ophanie Area Rugs Recalled Due to Fire Hazard; Violation of Federal Flammability Regulations; Sold Exclusively on…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ophanie
CPSC
Consumer productsReported Jul 25, 2024
Razor Recalls Icon Electric Scooters Due to Fall Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Razor USA LLC
CPSC
Consumer productsReported Jul 25, 2024
Toy Guns Recalled Due to Eye Injury Hazard; Failure to Meet Federal Safety Regulations for Projectile Toys; Sold…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shantoushi Chenghaiqu Youjiu Toy Factory
CPSC
Consumer productsReported Jul 25, 2024
Stiger Recalls Besrey Twins Strollers Due to Entrapment, Fall and Choking Hazards; Violation of Federal Regulation for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Stiger Inc.
CPSC
Consumer productsReported Jul 25, 2024
Textron Specialized Vehicles Recalls 2024 Arctic Cat Mountain 600 Snowmobiles Due to Crash Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Textron Specialized Vehicles
CPSC
Consumer productsReported Jul 25, 2024
Torquay eTrading Recalls Essential Values Golf Grip Solvent and Golf Grip Kits Due to Risk of Poisoning; Violation of…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Torquay eTrading LLC (dba Essential Values)
CPSC
Reported Jul 24, 2024
Abbott Proclaim XR 5 Implantable Pulse Generator, REF 3660, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Impella CP with SmartAssist, Product No.: 1000080 (REF 0048-0003). left heart support blood pump
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Surgical Image Guidance Functionality, software used with NGENUITY 3D Visualization System, Part Number: 8065000399
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Aurobindo Pharma USA, Inc. recalls Healthy Living Migraine Relief Acetaminophen 250mg, Aspirin (NSAID) 250mg & Caffeine 65mg tablets due to Device & Drug…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Aurobindo Pharma USA, Inc.
FDA (recalls & safety alerts)
Reported Jul 24, 2024
OUTLOOK IV SET 15DROP W/2 CARESITE-Used with an electrically-powered infusion pump for intravenous (IV) administration…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
28 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Volara System. Single Patient Use (SPU) Circuit 5kit for Volara and Single Patient Use (SPU) Circuit kit for Volara.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 24, 2024
BD Multitest 6-Color TBNK CE-IVD, REF: 644611; BD Multitest 6-Color TBNK Kit with BD Trucount Tubes CE-IVD, REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Biosciences
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Autotome RX 20mm CUT WIRE Cannulating Sphincterotome, Material Number (UPN) M00545170. The device is used in selective…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Oatmeal Daily Moisturizing Body Lotion (1.3% Dimethicone), 8 fl oz (236mL), packaged in an HDPE bottle 12 bottles per…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brands International Corporation
FDA (openFDA drug enforcement)
Reported Jul 24, 2024
Cascade IOMAX Cortical Module, REF: 190296-200
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cadwell Industries Inc.
FDA (openFDA device enforcement)
Reported Jul 24, 2024
Product Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canadian Hospital Specialties Ltd.
FDA (openFDA device enforcement)
Reported Jul 24, 2024
BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
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