Recall archive
31,892 recalls · page 218 of 1329
Consumer productsReported Sep 19, 2024
Jo-Ann Stores Recalls Place & Time Battery-Operated Desk Lamps Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jo-Ann Stores LLC
CPSC
Reported Sep 19, 2024
KTM Services Inc recalls Enjoy Premium Coconut and Taro Cookies due to Undeclared milk allergen
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.KTM Services Inc.
FDA (recalls & safety alerts)
Consumer productsReported Sep 19, 2024
Children's Jewelry Sets Recalled Due to Risk of Lead and Cadmium Poisoning; Violations of the Federal Lead Content Ban…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Memovan Technology Industrial Co. Limited, (dba Newmemo)
CPSC
Consumer productsReported Sep 19, 2024
Polaris Recalls Sportsman All-Terrain Vehicles Due to Fire Hazard
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 Sep 19, 2024
Wee Gallery Recalls Baby Tummy Time Gallery Due to Violation of the Federal Phthalates Ban
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Wee Gallery Inc.
CPSC
Consumer productsReported Sep 19, 2024
Ceither Adult Portable Bed Rails Recalled Due to Serious Entrapment and Asphyxia Hazards; Violation of Federal…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Yangkeqiang, dba Inforce
CPSC
Reported Sep 18, 2024
American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Outdoor Products, Inc.
FDA (openFDA food enforcement)
Reported Sep 18, 2024
Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U
High riskUsing this product could cause serious injury, illness or death — stop using it now.B Braun Medical Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Guidewire 70cm x 1mm (0.038 ) REF 5583705 These accessories are intended for use with Bard 14.5 Fr. Long-Term Dual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Bionpharma Inc. recalls BionPharma Atovaquone Oral Suspension, 750 mg/mL due to Product found to be contaminated with Cohnella bacteria
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Bionpharma Inc.
FDA (recalls & safety alerts)
Reported Sep 18, 2024
Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz (97g), Rx Only, Manufactured for Elevate Oral…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Elevate Oral Care
FDA (openFDA drug enforcement)
Reported Sep 18, 2024
6.5oz Emerald Kettle Glazed Walnut, UPC: 0 10300 80894 7
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flagstone Foods, LLC
FDA (openFDA food enforcement)
Reported Sep 18, 2024
Blood Pressure Module BPM3 TM-2917B (Spare Part Numbers 191378 or 191389) with firmware version S005 installed in 2008…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A Software Version: N/A Product Description: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi America, Ltd., Particle Therapy Division
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
IBA Proton Therapy System - PROTEUS 235 ProteusPLUS and ProteusONE Software versions: PTS-8 versions, PTS-10 versions,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Yummy Monkey Organics Butter & Yeast Popcorn, Made With Purified Ghee & Nutritional Yeast. UPC 9 96692 66641 2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kester Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 18, 2024
Foam Protective Pouches, model numbers 6010 (50 each/case), 6010-1 (350 each /case), 6060 (8 rolls/case), 6070 (75…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Action Industries, Inc. 306
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Medline Convenience kits, labeled as: 1) TRACHEOTOMY TRAY, Pack Number DYNDA1894; 2) ULTRASOUND GUIDED PIV KIT, Pack…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
105 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Medtronic Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Medtronic DLP Single Stage Venous Cannulae with right angle metal tip, REF 67312
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Medtronic ENT Ultra Round Steel Cutting Bur, Model Number REF 31313069
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Xomed, Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2024
Olympus Triangle Tip Electrosurgical Knives- to be used with Olympus endoscopes and electrosurgical units to cut tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 18, 2024
BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC 7189147148, Orwaiian LLC, 465 NE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orwaiian LLC
FDA (openFDA food enforcement)
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