burn risk Recalls

425 recalls tagged with “burn risk”.

Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Humeral Head Plate MRI Recall Affects 292 Units in 2026

ITS GmbH recalled 292 proximal humeral plates nationwide in the United States after MRI safety testing showed higher RF-induced heating under certain MRI conditions. The heating can occur during MRI and may cause burns or tissue damage. Patients and clinicians should stop using the device immediately and follow the recall instructions from ITS GmbH and their healthcare providers.

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

I.T.S. Ulna Locking Plate Systems Recalled Over MRI Heating Risk (2026)

I.T.S. GmbH recalled 120 units of its DUL and UOL ulna locking plate systems distributed nationwide to U.S. healthcare providers after MRI safety testing showed higher RF-induced heating. The updated testing found temperature increases under certain MRI conditions not reflected in the Instructions for Use. Healthcare facilities and patients should stop using the devices immediately and follow the厂

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

Dukal BZK Antiseptic Towelettes Recalled for CGMP Deviations (2026)

Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.

Dukal
CGMP Deviations
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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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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

Integra LifeSciences Corp. recalled 55,276 units of MEDIHONEY Calcium Alginate with Active Leptospermum Honey on January 16, 2026. The recall cites potential packaging failures that may compromise sterility. Affected products include model numbers 31012, 31022, and 31045.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls MediHoney Gel for Packaging Issues

Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Integra LifeSciences Corp.
Potential packaging
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Recalled Asher Pajama Set
HIGH
CPSC

Morgan Lane Recalls Children's Pajama Sets Over Burn Hazard

Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.

Morgan Lane
The recalled
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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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Food & Beverages
HIGH
FDA FOOD

WinCo Foods Recalls Deli Margherita Pizza Due to Metal Fragments

WinCo Foods recalled 5,066 cases of Deli Margherita Pizza on January 15, 2026, due to potential metal fragments. The affected item is a 17oz Take & Bake pizza. Consumers should not consume the product and seek refunds immediately.

WinCo Foods
Product may
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Health & Personal Care
HIGH
FDA DEVICE

FUJIFILM Healthcare Recalls X-ray Generator Over Fire Hazard

FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.

FUJIFILM Healthcare Americas
It was
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Recalled Isla Rae Magnetic Wireless Charger (white)
HIGH
CPSC

Isla Rae Magnetic Wireless Chargers Recalled Over Fire Hazard

Isla Rae recalled magnetic wireless chargers on January 8, 2026, due to risks of fire and burn hazards. Consumers should stop using the chargers immediately and seek refunds. The chargers were sold at T.J. Maxx and Marshalls locations between June 2024 and November 2025.

Isla Rae Magnetic Wireless Chargers
The chargers
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Medical Device Recalled Over Deformation Risk

Olympus Corporation recalled 4,183 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. Devices may deform and lose performance due to inadequate thermoforming. Healthcare providers should immediately stop using the affected products and follow recall instructions.

Olympus Corporation of the Americas
Devices which
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Sphincterotome Over Deformation Risk

Olympus Corporation of the Americas recalled 93 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to a manufacturing flaw. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Devices which
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Sphincterotome Over Performance Risks

Olympus Corporation of the Americas recalled 5,946 single use sphincterotomes on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must cease use immediately to avoid potential hazards.

Olympus Corporation of the Americas
Devices which
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Sphincterotome Recalled Due to Deformation Risk

Olympus Corporation recalled 1,474 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform and lose performance due to improper thermoforming. Healthcare providers and patients must stop using these instruments immediately.

Olympus Corporation of the Americas
Devices which
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Tag Statistics

Total Recalls
425

Related Tags

adult productimmediate actionstop use immediatelyfda regulatednhtsa regulatedcpsc regulatedelectronicmetalreplacement availableliving roominfant productfire hazard