Fire and burn hazard recalls
A notice appears here when the stated hazard is fire, burning, overheating or a lithium-ion battery failure. These are the recalls where agencies most often say to stop using the product immediately rather than wait for a replacement part — the notice itself says which.
1,108 stored notices, reported between Jun 27, 2012 and Sep 17, 2026. Newest first.
Consumer productsReported Mar 4, 2015
Melville Direct Recalls Aquarium Motion Lamps Due to Fire Hazard; Sold Exclusively by Bits & Pieces (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Melville Direct
CPSC
Consumer productsReported Feb 24, 2015
Safe Step Walk-In Tubs Recalled by Oliver Fiberglass Products and NuWhirl Systems Due to Burn Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oliver Fiberglass Products
CPSC
Consumer productsReported Feb 18, 2015
Hayneedle Recalls Fiber Optic Lighted Christmas Trees Made by East-West Basics Due to Fire Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.East-West Basics
CPSC
Consumer productsReported Feb 12, 2015
Jackco Transnational Recalls ZETA Battery Pack Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jackco Transnational, Inc.
CPSC
Reported Feb 11, 2015
LINAC Accelerators: ARTISTE, ONCOR Avant Garde, ONCOR Impression Plus, ONCOR Expression, ONCOR Impression, PRIMUS HI,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Consumer productsReported Feb 4, 2015
Children's Pajamas and Robes Recalled by Lazy One Due to Violation of Federal Flammability Standard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lazy One, Inc.
CPSC
Consumer productsReported Jan 28, 2015
Vosges Haut-Chocolat Recalls Festival of Lights Gift Box Sets Due to Fire Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vosges Haut-Chocolat
CPSC
Consumer productsReported Jan 27, 2015
Mirka Extends Recall of Compact Electric Random Orbital Sanders Due to Fire Hazard
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mirka Abrasives, Inc.
CPSC
Consumer productsReported Jan 21, 2015
La-Z-Boy Recalls Control Wands Sold With Silver Luxury Lift Chairs Due to Burn Hazard (Recall Alert)
High riskUsing this product could cause serious injury, illness or death — stop using it now.La-Z-Boy Incorporated
CPSC
Consumer productsReported Jan 8, 2015
CoScentrix Expands Recall of DD Brand Candles Due to Fire Hazard; Exclusively at Hobby Lobby
High riskUsing this product could cause serious injury, illness or death — stop using it now.CoScentrix
CPSC
Reported Dec 31, 2014
Component- Dianz Capacitor used in PerfectO2 Oxygen Concentrator, packaged one unit per box.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Sep 10, 2014
Hitachi Echelon Oval MRI system is a diagnostic imaging device (one unit per package) and is intended to provide the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Patient Side Cart Battery Box used in conjunction with the da Vinci A surgical system. Intuitive Surgical Inc.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 16, 2014
Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Stirling Ultracold Portable Shuttle, ULT-25. Storage for cold-chain management, short-term or long-term ultra-low and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Global Cooling Inc.
FDA (openFDA device enforcement)
Reported Jul 9, 2014
Siemens Mobilett XP Digital Mobile X-ray System Product Usage: The Mobilett XP and Mobilett XP Hybrid are radiographic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jul 2, 2014
IF 8000; 1/F Interferential Electrical Stimulation Device; NMES (neuromuscular electrical stimulation) mode. Designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zynex Medical, Inc.
FDA (openFDA device enforcement)
Reported May 28, 2014
Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic Balloon Pump (IABP) is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maquet Datascope Corp. - Cardiac Assist Division
FDA (openFDA device enforcement)
Reported May 28, 2014
Lithium Ion Battery M4605A and M4607A for use with IntelliVue Patient Monitors. The monitor is used for monitoring and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Apr 30, 2014
GE Healthcare, Discovery MR450, Discovery MR750, Optima MR450w, Optima MR 450w GEM, Discovery MR750w, and Discovery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2013
Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Cardiovascular, LLC
FDA (openFDA device enforcement)
Reported Oct 23, 2013
Getinge 46-Series Medical Washer-Disinfectors, Listing # E208196 Product Usage: The washer disinfector is used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Getinge Disinfection
FDA (openFDA device enforcement)
Reported May 15, 2013
Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus America Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Nicolet EEG Wireless Amplifier 32/64 Channel. Catalog/Part Numbers : 515-015400 for the 32 channel amplifier and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology Incorporated
FDA (openFDA device enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.