immediate action Recalls

2,756 recalls tagged with “immediate action”.

Food & Beverages
HIGH
FDA FOOD

SB FOOD Recalls Gummy Candy Due to Unsafe Color Additive

SB FOOD recalled 100 cases of Yoyo Gummy Tropical Flavor on November 21, 2025. The products contain an unallowed color, Carmoisine (E122), posing health risks. Consumers in 14 states should stop consuming the product immediately.

SB FOOD
The products
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination

Glenmark Pharmaceuticals recalled over 11,000 bottles of Bisoprolol Fumarate and Hydrochlorothiazide Tablets on November 21, 2025. Testing revealed traces of ezetimibe, posing a health risk. Consumers should stop using the product immediately and contact their healthcare provider.

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
Cross Contamination
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Food & Beverages
HIGH
FDA FOOD

Ambriola Grated Pecorino Romano Recalled Due to Listeria Risk

Ambriola Co., Inc. recalled 6,632 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a dangerous bacteria that can cause serious illness. Consumers should not consume the affected product and should seek refunds or replacements.

Ambriola Co., Inc.
Product tested
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Food & Beverages
HIGH
FDA FOOD

Ambriola Piccante Grated Pecorino Romano Recalled for Listeria Risk

Ambriola Co., Inc. recalled 179 bags of grated Pecorino Romano on November 21, 2025. The product tested positive for Listeria Monocytogenes, prompting immediate consumer action. It was distributed across 15 states, including California and Texas.

Ambriola Co., Inc.
Product tested
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Food & Beverages
HIGH
FDA FOOD

Ambriola Grated Pecorino Romano Recalled Due to Listeria Risk

Ambriola Co., Inc. recalled 45 bags of Pinna Grated Pecorino Romano on November 21, 2025, after Listeria Monocytogenes was detected. The recall affects products distributed in 17 states including California and Texas. Consumers should not consume the recalled product and should seek refunds or replacements.

Ambriola Co., Inc.
Product tested
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Food & Beverages
HIGH
FDA FOOD

Lotus Mom Corporation Recalls Aluminum Kadai Over Lead Contamination

Lotus Mom Corporation recalled 43 units of its Aluminum Kadai on November 21, 2025, due to potential lead contamination. Consumers should avoid using the product and seek refunds or replacements. The recall affects distribution in California and Colorado.

Lotus Mom Corporation dba Indian Kitchen Mart
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Lotus Mom Corporation Recalls Brass Tope Due to Lead Contamination

Lotus Mom Corporation recalled 10 units of Brass Tope on November 21, 2025, due to potential contamination with leachable lead. Consumers should not use the product and seek refunds or replacements. The recall affects distribution in California and Colorado.

Lotus Mom Corporation dba Indian Kitchen Mart
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Fagron Compounding Services Recalls Ophthalmic Solution Over Incorrect Formulation

Fagron Compounding Services recalled 2,980 syringes of a topical ophthalmic solution on November 20, 2025. The recall stems from an incorrect product formulation that could pose health risks. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Fagron Compounding Services
Incorrect Product
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Recalled MoonSoll Ethanol Fuel Bottle
HIGH
CPSC

Demlar Recalls MoonSoll and Magic Chems Fuel Bottles Over Flash Fire Risk (2025)

Demlar recalled MoonSoll ethanol and Magic Chems bioethanol fuel bottles sold online by the Demlar Online Store. The bottles lack flame mitigation devices required by the Portable Fuel Container Safety Act, creating a flash-fire risk. Consumers should stop using the recalled bottles immediately and contact Demlar for a full refund.

Demlar
The ethanol
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Recalled Spartan Riding Lawn Mower (SRT-XD)
MEDIUM
CPSC

Spartan Mowers Recalls 2025 SRT-XD and KGZ-XD Riding Mowers for Steering Damper Hazard

Spartan Mowers recalled certain Model Year 2025 SRT-XD and KGZ-XD zero-radius-turn riding mowers sold through Spartan dealers nationwide. A steering arm damper can be installed incorrectly, creating a bouncing motion and loss of operator control. Owners should stop using the recalled mowers and contact an authorized Spartan dealer for a free inspection and repair.

Spartan Mowers and UTVs
The riding
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Recalled Play Yard
HIGH
CPSC

Anna Queen Play Yard Recall 2025 for Suffocation Risk on Amazon

Anna Queen recalls Play Yards sold on Amazon due to suffocation and entrapment risks. The product features black fabric sides, gray mesh panels, and white top rails with a bear-print design. Model P700 and production date 202503 appear on packaging and a removable tag. Consumers should stop using recalled units and obtain a full refund from Anna Queen.

Play Yards
The play
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Recalled Anzmtosn Magnet Fidget Spinner Set
HIGH
CPSC

Anzmtosn 15-Piece Magnet Fidget Spinner Sets Recalled for Ingestion Risk (2025)

Anzmtosn recalled 15-piece Magnet Fidget Spinner Sets sold on Amazon after magnets pose a serious ingestion hazard. The magnets can detach and, if swallowed, attract each other or metal objects and cause internal injuries. Stop using the sets now and email disposal photos to Anzmtosn53@163.com for a full refund.

Anzmtosn
The recalled
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Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Baby Soothe Herbal Supplement Over Misbranding

A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

A New Life Herbs
Unapproved drug
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Food & Beverages
HIGH
FDA FOOD

A New Life Herbs Recalls Chaga Mushroom Supplement Over Misbranding

A New Life Herbs, LLC recalled 144 bottles of Chaga Mushroom Herbal Supplement on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

A New Life Herbs
Unapproved drug
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Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Sinus Cap Herbal Supplement Over Misbranding

A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.

A New Life Herbs
Unapproved drug
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Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Baby Allergy Herbal Supplement Over Label Issues

A New Life Herbs, LLC recalled 23 bottles of its Baby Allergy Herbal Supplement on November 20, 2025. The recall follows unapproved drug claims and absence of a Supplement Facts label on the product. Consumers should not consume the supplement and should seek refunds immediately.

A New Life Herbs
Unapproved drug
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Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Ear Drops Over Misbranding Issues

A New Life Herbs, LLC recalled 22 bottles of Mullein flower alcohol tincture on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using this product immediately.

A New Life Herbs
Unapproved drug
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