Recall archive
31,892 recalls · page 299 of 1329
Consumer productsReported Nov 30, 2023
GE Appliances, a Haier Company, Recalls Electric Cooktops Due to Burn Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Haier US Appliance Solutions Inc., d/b/a GE Appliances
CPSC
Consumer productsReported Nov 30, 2023
Peg Perego Recalls Inclined Sleeper Bassinets for YPSI and Z4 Strollers Due to Risk of Suffocation and Fall Hazard;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Peg Perego SPA
CPSC
Consumer productsReported Nov 30, 2023
Polaris Recalls Patriot 9R MATRYX PRO RMK and Patriot 9R MATRYX RMK KHAOS Snowmobiles Due to Injury Hazard (Recall…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Polaris Industries Inc.
1 more product in this recall
CPSC
Consumer productsReported Nov 30, 2023
Russound Recalls AW70V6 Loudspeakers Due to Impact Injury Injury Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Russound/FMP Inc.
CPSC
Consumer productsReported Nov 30, 2023
Klickpick Home Recalls Stainless Steel Children's Cup Sets Due to Violation of Federal Lead Content Ban; Sold…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Shree Ashtavinayak LLC, dba Klickpick Home
CPSC
Consumer productsReported Nov 30, 2023
Specialized Bicycle Components Recalls Supacaz Brand Orbitron Pedals Due to Fall Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Specialized Bicycle Components Inc.
CPSC
Reported Nov 29, 2023
ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26), UPC: 363102217104.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.ActiPharma, Inc.
FDA (openFDA food enforcement)
Reported Nov 29, 2023
Bronchoscope-for endoscopy and endoscopic surgery within the airways and tracheobronchial tree. Model Numbers:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aizu Olympus Co., Ltd.
21 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Asenzya Hot & Spicy Cajun Style Seasoning, Item 121331. Net Wt 15 lbs. Distributed by: Asenzya 7616 South Sixth Street,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Asenzya Inc.
FDA (openFDA food enforcement)
Reported Nov 29, 2023
AVANOS BALLARD Closed Suction System for Adults, 14 Fr, DSE, MDI, Product code 221038, provide suction on patients on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Avanos Medical, Inc.
FDA (openFDA device enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Compress Device Segmental Anchor Plug, 10 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
LEADER brand Eye Irritation Relief (Polyvinyl alcohol 0.5%, Povidone 0.6%, Tetrahydrozoline Hydrochloride 0.05%), 0.5…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health Inc.
5 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Convergent Dental
FDA (openFDA device enforcement)
Reported Nov 29, 2023
8.4% Sodium Bicarbonate Injection, USP, 50 mEq/50 mL (1mEq/mL), a) 20x50 mL Single Dose Vials (Vial NDC 51754-5001-1;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Exela Pharma Sciences LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
Esomeprazole Magnesium Delayed-Release Capsules, USP 20mg, Packaged as (a) 30-count bottle, NDC 68462-390-30; (b)…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Glenmark Pharmaceuticals Inc., USA
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Part Numbers 00024307504, 00024330004, 00024345004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Integrity Biochem HSC 70-LM, Alcohol Antiseptic 70%, Hand Sanitizer, Lemon Scented Topical Gel, 208.19 L (55 gallons)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integrity Bio-Chemicals LLC
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
Tiglutik (riluzole) Oral Suspension 50 mg/10 mL (5 mg/mL), 600 mL (two bottles/300 mL each), RX only, Manufactured for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Itf Pharma Inc.
FDA (openFDA drug enforcement)
Reported Nov 29, 2023
Jeni's Splendid Ice Cream: Buttercream Birthday Cake Ice Cream packaged in paperboard pint cups with heat seals and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jeni's Splendid Ice Creams LLC
FDA (openFDA food enforcement)
Reported Nov 29, 2023
ORION System with software OSS v6.0 and OSS v7.0- An electro-mechanical robotic arm for patient positioning in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leoni Cia Cable Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Medtronic Mo.Ma Ultra Proximal Cerebral Protection Device, Model Number MUS0130069X6
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
2 more products in this recall
FDA (openFDA device enforcement)
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