Recall archive
31,892 recalls · page 306 of 1329
Consumer productsReported Nov 2, 2023
Grizzly Industrial Recalls Wood Lathes Due to Injury and Laceration Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grizzly Industrial Inc.
CPSC
Consumer productsReported Nov 2, 2023
Yoocaa Baby Loungers Recalled Due to Suffocation Risk and Fall and Entrapment Hazards; Fails to Meet Safety…
High riskUsing this product could cause serious injury, illness or death — stop using it now.He Nan Ji Bu Gong Yi Pin You Xian Gong Si, D/B/A Yoocaa Direct
CPSC
Consumer productsReported Nov 2, 2023
Lochinvar Recalls Condensing Boilers Due to Risk of Carbon Monoxide Poisoning
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lochinvar LLC
CPSC
Consumer productsReported Nov 2, 2023
Murf Electric Bikes Recalls Electric Bicycles Due to Fall and Injury Hazards (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Murf Electric Bikes LLC
CPSC
Consumer productsReported Nov 2, 2023
UncleWu Life Recalls Infant Bath Seats Due to Drowning Hazard; Violation of Bath Seat Requirements; Sold Exclusively on…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.UncleWu Life LLC
CPSC
Reported Nov 1, 2023
TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acclarent, Inc.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
General Pack, REF BBGP31C
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System
High riskUsing this product could cause serious injury, illness or death — stop using it now.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Betty Lou's Inc.
FDA (openFDA food enforcement)
Reported Nov 1, 2023
ION*Sinus Spray, 1 fl oz/ 30 mL, Manufactured by: ION* Biome Charlottesville, VA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Biomic Sciences, LLC dba ION Intelligence
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 1, 2023
Monoject 1 mL Tuberculin Syringe Luer-Lock Tip Soft Pack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health 200, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
OPMI LUMERA 300, REF 6137
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Suzhou Co., Ltd.
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Oxytocin synthetic, 30 Units added to 0.9% Sodium Chloride 500mL IV Bag (0.06 Units per mL), Rx only, Leiter…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Denver Solutions, LLC dba Leiters Health
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Nov 1, 2023
Whole cantaloupe, Brand name Kandy 11 count carton, 8 count carton, 9 count carton, 15 count carton d. Container…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eagle Produce LLC, dba Martori Farms
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Embrace2- Indicated for use as an adjunct to seizure monitoring of adults and children age 6 and up in home or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Empatica Srl
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Centricity PACS-IW, software versions V3.7.x through 3.7.3.9 SP3; Radiological Image Processing System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
SOZO Bilateral Arm L-Dex Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Impedimed Limited
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Maquet Acrobat-i Vacuum Stabilizer System Intended for use during performance of cardiac surgical procedures through a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Grafton DBM Crunch, Model Numbers: T44115, Demineralized Bone Matrix
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Sofamor Danek USA Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Omega Medical Imaging, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Organic Protein & 50 Superfoods Protein Powder with Probiotic - Chocolate flavor
High riskUsing this product could cause serious injury, illness or death — stop using it now.Orgain
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Penzeys Brady Street Cheese Sprinkle. Item 20756. net wt 2.2 oz (62g). Penzeys Spices, Wauwatosa, WI 53222.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penzeys, Ltd.
FDA (openFDA food enforcement)
Reported Nov 1, 2023
Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Preat Corp.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 1, 2023
Astral 100 and Astral 150 ventilators
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
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