burn risk Recalls

425 recalls tagged with “burn risk”.

Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026

Philips Medical Systems Nederland B.V. recalls 8 Allura Xper FD20/15 OR Tables worldwide due to a risk that X-ray imaging may not start or may stop intermittently when using the wired foot switch. The issue is tied to System Code 722059 and requires immediate action. Hospitals and patients should stop using the device and follow the manufacturer’s recall instructions.

Philips
Philips has
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Health & Personal Care
HIGH
FDA DRUG

K.C. Pharmaceuticals Sterile Eye Drops Recall 315,144 Bottles for Lack of Sterility (2026)

K.C. Pharmaceuticals recalled 315,144 sterile eye drop bottles distributed nationwide after lack of sterility. The products span several brands including GNP Eye Drops Redness and Dry Eye Relief, Leader Eye Drops Redness Relief, and Foster & Thrive Redness Relief Eye Drops. Consumers should stop using the products immediately and follow guidance from KC Pharmaceuticals or their healthcare provider

GNP Eye Drops Redness and Dry Eye Relief
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Olympus SOLTIVE Premium Laser System Recall Affects 408 Units Worldwide (2026)

Olympus recalls 408 SOLTIVE Premium Laser System units worldwide after a defect in the 24V power supply may render the system inoperable and cause smoke or a burning smell. The issue is contained within the internal console and would self-extinguish. Hospitals should stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Following a
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Health & Personal Care
HIGH
FDA DEVICE

Olympus SOLTIVE Pro Laser System Recall 2026 — 32 Units Worldwide

Olympus recalled 32 SOLTIVE Pro SuperPulsed Laser System units distributed worldwide after a defect in the 24V power supply may render the device inoperable. The defect can cause smoke or a burning smell, but the issue is contained within the laser console enclosure and self-extinguishing. Stop using the device and follow the manufacturer’s recall instructions.

Olympus
Following a
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Recalled TheKiddoSpace LED Soccer Hover Ball
HIGH
CPSC

TheKiddoSpace Recalls LED Soccer Hover Balls Over Burn Risk

TheKiddoSpace recalled LED soccer hover balls on February 26, 2026, due to a burn hazard. The balls exceed the allowable surface temperature for batteries, posing serious injury risks. Consumers should stop using these toys immediately and seek a replacement.

TheKiddoSpace
The surface
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Recalled Dupray Neat Steam Cleaner
HIGH
CPSC

Dupray Recalls Neat Steam Cleaners Over Burn Hazard Risk

Dupray USA recalled portable Neat Steam Cleaners on February 26, 2026, due to burn hazards. The model number is DUP020WNA, with batch codes from 0118-01 to 0425-05. Consumers should stop using the product immediately and follow safety instructions for a free replacement part.

Dupray USA
The steam
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Recalled Royal Oak Flame Saber Lighter
HIGH
CPSC

Royal Oak Recalls Lighters Over Serious Fire and Burn Hazards

Royal Oak Enterprises recalled flame saber lighters on February 26, 2026, due to serious fire and burn hazards. The lighters lack child-resistant mechanisms and violate labeling requirements. Consumers should stop using these lighters immediately and seek a refund.

Royal Oak Enterprises
The recalled
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Recalled Somgem Lightweight Tiny Pinky Pig Lighter
HIGH
CPSC

Somgem and Yomin Toilet Lighters Recalled for Fire Hazard

Somgem and Yomin recalled pig and toilet lighters on February 26, 2026. The lighters lack child-resistant features, posing serious burn risks. Consumers should stop using these products immediately and seek refunds.

Somgem Pig and Yomin Toilet Lighters
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Atellica CH A1c_E Recall for 21,291 Units (2026)

Siemens Healthcare Diagnostics recalled 21,291 Atellica CH A1c_E units distributed to laboratories nationwide and internationally in 2026. The recall addresses a depressed result bias when A1c_E is processed with RCRP on the same analyzer. Labs using separate analyzers are not impacted. Stop using the affected module immediately and follow manufacturer instructions. Contact Siemens or your lab’s F

Siemens Healthcare Diagnostics
A potential
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Recalled Joly's 80% Vinegar (32 oz, pack of two) Product packaging
HIGH
CPSC

Joly's Recalls 80% Vinegar Due to Poisoning and Burn Risks

Joly's LLC recalled 80% Vinegar on February 19, 2026, due to serious risks of poisoning and chemical burns. The product lacks essential warning labels and first aid instructions, violating federal safety laws. Consumers should stop using the product immediately and seek a refund.

Joly's LLC, of Orlando, Florida
The recalled
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Recalled MCS one-piece footed sleepwear - Style 7903815
HIGH
CPSC

Meijer Recalls Children's Sleepwear Due to Burn Hazard

Meijer recalled several styles of children's sleepwear on February 19, 2026, due to a burn hazard. The recall affects various one-piece footed sleepwear for infants sizes 12, 18, and 24 months. Consumers should stop using the sleepwear and return it for a full refund.

Meijer
The recalled
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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

Medtronic MiniMed Paradigm Real-Time Insulin Pump Recalled for 29,074 Units Worldwide (2026)

Medtronic MiniMed recalled 29,074 Paradigm Real-Time insulin pumps worldwide. The devices may deliver insulin improperly when the pump is elevated or lowered relative to the infusion site due to gravitational effects. Patients should stop using the pumps immediately and follow recall instructions from the manufacturer and their healthcare provider.

Medtronic MiniMed
All Medtronic
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Food & Beverages
HIGH
FDA FOOD

Juniper Granola Junebar Recall 2026: 1,800 Snack Bars Recalled for Undeclared Milk and Soy

Juniper Granola recalled 1,800 Junebar Chocolate Cherry All Natural Snack Bars sold in New York after undeclared milk and soy were found. The bars carry Lot L1300 and variants L1300A and L1300B. They were produced in a facility that also processes gluten, peanuts, and sesame. Consumers should not eat these bars and should contact Juniper Granola for refunds or replacements.

Juniper Granola
Products contain
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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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Tag Statistics

Total Recalls
425

Related Tags

electrical hazardimmediate actionstop use immediatelytip over risklaceration riskfederal law violationreturn for refundfda regulatedcpsc regulatedelectronicbattery poweredinfant product