Recall archive
31,892 recalls · page 376 of 1329
Reported Dec 28, 2022
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Young Dental Manufacturing I, LLC
FDA (openFDA device enforcement)
Reported Dec 27, 2022
GFA Production recalls Multiple brand names After Burn® Cream and First Aid Kits containing After Burn Cream due to Product is contaminated with Bacillus…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.GFA Production
FDA (recalls & safety alerts)
Consumer productsReported Dec 22, 2022
Nova Medical Products Recalls Adult Bed Rails Due to Serious Entrapment and Asphyxia Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bliss Health Products Co. Ltd.
CPSC
Consumer productsReported Dec 22, 2022
BLU3 Recalls Nomad Battery-Powered Tankless Diving Systems Due to Drowning Hazard for Divers
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blu3
CPSC
Consumer productsReported Dec 22, 2022
KTM North America Recalls GASGAS Off-Road Motorcycles Due to Crash and Injury Hazards
High riskUsing this product could cause serious injury, illness or death — stop using it now.KTM North America Inc.
CPSC
Reported Dec 22, 2022
Morasch Meats Inc. Recalls Raw Frozen Diced Beef Products Due to Possible E. Coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Morasch Meats, Inc.
USDA FSIS
Consumer productsReported Dec 22, 2022
Pacific Cycle Recalls Pacific Kids' Igniter and Pacific Bubble Pop 20-Inch Bicycles Due to Fall Hazard; Sold…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pacific Cycle Inc.
CPSC
Consumer productsReported Dec 22, 2022
Samsung Recalls Top-Load Washing Machines Due to Fire Hazard; Software Repair Available
High riskUsing this product could cause serious injury, illness or death — stop using it now.Samsung Electronics America Inc.
CPSC
Consumer productsReported Dec 22, 2022
Target Recalls Children's Pillowfort Weighted Blankets Due to Asphyxiation Hazard; Two Fatalities Reported
High riskUsing this product could cause serious injury, illness or death — stop using it now.Target Corporation
CPSC
Reported Dec 21, 2022
CarePoint 60 mL Syringe Without Needle, REF: 04-7560
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Allison Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
High riskUsing this product could cause serious injury, illness or death — stop using it now.ARROW INTERNATIONAL Inc.
32 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Neuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6 mL) bottles, Mfg.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Atlantic Management Resources Ltd.
3 more products in this recall
FDA (openFDA drug enforcement)
Reported Dec 21, 2022
Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml, Total Volume 8 ml in 10 ml syringe, 5-count syringes packaged in a bag…
High riskUsing this product could cause serious injury, illness or death — stop using it now.BayCare Integrated Service Center, LLC /dba BayCare Central Pharmacy
FDA (openFDA drug enforcement)
Reported Dec 21, 2022
BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Lacosamide Oral Solution, USP, CV, 10mg/mL, packaged in 200 mL bottle, Rx Only, Manufactured for: Camber…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Camber Pharmaceuticals, Inc.
FDA (openFDA drug enforcement)
Reported Dec 21, 2022
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Cordis Angiographic Catheter Extensions. Used to transport fluid from the power injector to the catheter for injection…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis US Corp.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
DeRoyal MINOR ORAL / ENT PACK, REF 89-2576.15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DeRoyal Industries Inc.
155 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Oncentra Brachy radiation therapy planning system software.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
PDS II (polydioxanone) Suture- VIOLET MONOFILAMENT 27IN 0 S/A CT-1 Product Code: Z340H For use in soft tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon, Inc.
FDA (openFDA device enforcement)
Reported Dec 21, 2022
8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Exela Pharma Sciences LLC
1 more product in this recall
FDA (openFDA drug enforcement)
Reported Dec 21, 2022
Leica MICROSYSTEMS Proveo 8, Part Number 10449058, surgical microscope system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 21, 2022
Lupin Pharmaceuticals Inc. recalls Lupin Quinapril 20 and 40 mg tablets due to Presence of nitrosamine impurity, N-Nitroso-Quinapril
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Lupin Pharmaceuticals Inc.
FDA (recalls & safety alerts)
Reported Dec 21, 2022
NUVASIVE MAGEC MAGEC 2 Rod. The MAGEC System is used to brace the spine during growth to minimize the progression of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NuVasive Specialized Orthopedics, Inc.
FDA (openFDA device enforcement)
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