fire hazard Recalls

250 recalls tagged with “fire hazard”.

Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Garlic & Herb Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads Inc recalled 557 five-pound tubs of Garlic & Herb Cream Cheese sold in New York after a confirmed Listeria monocytogenes contamination. The recall was activated on February 19, 2026 and remains active as of March 18, 2026. Consumers who purchased the product should not consume it and should contact the company for refund or replacement guidance.

Made Fresh Salads
Products may
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.

Mentor
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medline Industries, LP recalled 14,379 Airway Exam Kits containing Olympus biopsy valves nationwide. The recall cites rubber fragments detaching from the slit of single-use biopsy valves. Potential harm includes a foreign body in the patient’s tracheobronchial tree, inflammatory response, hypoxia, and longer procedures. Providers and patients should stop using the kit and follow recall directions.

Medline Industries, LP
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-1443/MAJ-1444 Endoscope Suction Valves Recalled in 2026

Olympus Corporation of the Americas recalls 47,383 MAJ-1443 and MAJ-1444 endoscope suction valves distributed nationwide in the United States. The valves are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors. Hospitals and clinics should stop using the valves immediately and follow the manufacturer’s recall instructions.

Olympus Corporation of the Americas
The MAJ-1443
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Recalled LSHOME 3-Pack Smoke Detector Fire Alarm packaging
HIGH
CPSC

LShome Smoke Detectors Recalled Over Failure to Warn During Fire

LShome recalled 3-Pack Smoke Detector Fire Alarms on February 12, 2026, due to a failure to warn during a fire. The defect poses a serious risk of injury or death. Consumers should stop using these alarms immediately and contact the manufacturer for a refund.

LShome Photoelectric Smoke Detector Fire Alarms
If the
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Recalled Aroeve MK04 Air Purifier in white
HIGH
CPSC

Airova Recalls Aroeve Air Purifiers Due to Fire Hazards

Airova recalled Aroeve air purifiers on February 9, 2026, due to fire and burn hazards. The recall affects model MK04 with serial numbers starting with 'BN' manufactured before July 2025. Consumers should stop using these air purifiers immediately and seek replacements.

Airova
The air
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Recalled Scepter B62 Gas and Oil Fuel Container – front
HIGH
CPSC

Scepter B62 Gas and Oil Fuel Containers Recalled for Flash Fire Risk (2026)

Scepter B62 dual-chamber fuel containers imported by Mameix Retail are recalled for a flash fire and child poisoning risk. The recall cites a lack of flame-mitigation devices and a non–child-resistant spout. Consumers should stop using the recalled containers and contact Mameix Retail for a full refund.

Scepter
The recalled
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NorthStar Gas Wet Steam and Hot Water Pressure Washer (Item #157310)
HIGH
CPSC

Northern Tool Recalls Hot Water Pressure Washers Over Fire Risk

Northern Tool + Equipment recalled three models of hot water pressure washers on January 29, 2026. Abnormal burner operation can produce smoke and flames, posing a fire hazard. Consumers should stop using the products immediately and seek repairs.

Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
The fan
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026

I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Pilon Plate with Angular Stability Recalled for MRI Heating Risk (2026) 101 Units

ITS GmbH recalls 101 Pilon Plate with Angular Stability implants distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

I.T.S. GmbH
Updated MRI
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Recalled Matrix Retail T30 (TM729) Treadmill
HIGH
CPSC

Johnson Health Tech Expands Treadmill Recall Over Fire Hazard

Johnson Health Tech expanded its recall of Matrix and Vision treadmills due to fire hazards. The affected models include T30, TF30, T50, TF50, T75, and others. Consumers should stop using these treadmills immediately and check for a power cord bracket.

Johnson Health Tech Expands
The power
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Health & Personal Care
HIGH
FDA DRUG

Medi-First Antiseptic Wipes Recalled for CGMP Deviations in 2026, 100 Wipes per Box

ACME United Corporation recalled Medi-First Antiseptic Wipes sold nationwide in the United States. The recall cites CGMP deviations that could affect product quality. Consumers and healthcare providers should stop using the wipes immediately and contact ACME United Corporation or a healthcare provider for guidance.

Medi-First Antiseptic Wipes
CGMP Deviations
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Food & Beverages
HIGH
FDA FOOD

Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)

Bader Enterprises recalls 60 pounds of Premium Food Jordan Almonds sold in New Jersey and New York. The product contains undeclared wheat and blue color additives. Consumers who purchased the product should not consume it. Contact Bader Enterprises for refund or replacement information via two or more notification methods.

Bader Enterprises
Contains undeclared
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Recalled Curtis International Minifridge Model EFMIS121 – serial numbers between A2001 to A2310
HIGH
CPSC

Curtis International Recalls Frigidaire Minifridges Over Fire Risk

Curtis International recalled 50,000 Frigidaire-brand minifridges on January 15, 2026, due to fire and burn hazards. The recall affects model EFMIS121 and previously recalled models EFMIS129, EFMIS137, EFMIS149, and EFMIS175. Consumers should stop using these minifridges immediately and seek a refund.

ShangYu North Electron Manufacture Co. Ltd., of China
The minifridges'
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Tag Statistics

Total Recalls
250

Related Tags

chemical hazardpoisoning riskinfant productlaceration riskchoking hazardburn riskelectrical hazardstop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulated
    fire hazard Recalls | RecallRadar