burn risk Recalls

471 recalls tagged with “burn risk”.

Food & Beverages
HIGH
FDA FOOD

Ajinomoto Foods North America Recalls 35,955 Pounds of Japanese-Style Fried Rice for Glass Contamin‑

Ajinomoto Foods North America recalled 35,955 pounds of Ajinomoto Japanese-Style Vegetable Fried Rice distributed by multiple retailers in 43 states after glass fragments were found in the product. The glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers who bought the product should not eat it and should contact Ajinomoto Foods North America for a refund or replacement.

Ajinomoto Foods North America
Foreign objects
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Kroger Chinese Inspiration Fried Rice Recalled for Glass Contamination (2026)

Ajinomoto Foods North America recalled 109,741 cases of Kroger Chinese Inspiration Vegetable Fried Rice sold at Kroger stores after glass fragments were found. Glass pieces measure 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat this product and should seek a refund or replacement from Ajinomoto Foods North America.

Ajinomoto Foods North America
Foreign objects
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Food & Beverages
HIGH
FDA FOOD

Ajinomoto Green Gyoza Dumplings Recalled for Glass Shards in 537,033 Lbs (2026)

Ajinomoto Foods North America recalls 537,033 pounds of Ajinomoto Green Gyoza Vegetable & Edamame Dumplings sold nationwide after glass fragments were found. Glass pieces range from 1 to 3 cm long and 2 to 4 mm wide. Consumers should not eat the recalled dumplings and should contact Ajinomoto Foods North America for a refund or replacement.

Ajinomoto Foods North America
Foreign objects
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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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Health & Personal Care
HIGH
FDA DEVICE

Spacelabs Healthcare 91496 Multi-parameter Module Recall Affects 1,790 Units Worldwide (2026)

Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.

Spacelabs Healthcare
Multi-parameter command
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic RA Syringe Recall Expands to 966 Kits Worldwide (2026)

Medline Industries, LP recalls 966 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers kits labeled DELIVERY PACK with SKUs DYNJ42892F and DYNJ42892G distributed worldwide, including the US and PR. The defect is a rotating adaptor that may unwind, creating a loose connection or disconnection between syringe and manifold. Stop using the device and use

Medline Industries, LP
Medline Industries,
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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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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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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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Tag Statistics

Total Recalls
471

Related Tags

glasslaceration riskpoisoning riskinfant productadult productpet relatedfederal law violationcpsc regulatedreturn for refundreplacement availablestop use immediatelyimmediate action