Food & Beverages Recalls

587 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Food & Beverages
HIGH
FDA FOOD

Baker's Authority Graham Cracker Meal Recalled Over Allergen Risks

Baker's Authority recalled 70 units of Graham Cracker Meal on August 12, 2025, due to undeclared allergens. The product lacks proper labeling for wheat and soy, posing a serious health risk to allergic consumers. These items were distributed across multiple states including NY, CA, and TX.

Bakers Authority
Product label
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Food & Beverages
HIGH
FDA FOOD

H & N Group Recalls Frozen Shrimp Over Contamination Risk

H & N Group recalled 17,214 cases of frozen shrimp on August 12, 2025. The product may be contaminated with Cesium-137 due to unsanitary manufacturing conditions. Consumers should not consume the shrimp and seek refunds immediately.

H & N Group
Product manufactured
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Food & Beverages
HIGH
FDA FOOD

SUNGAL Canned Half Plum Recalled Due to Cyclamate Contamination

SUNGAL recalled 29 cases of canned Half Plum on August 8, 2025, due to cyclamate adulteration. The affected product may pose a health risk. Consumers in California, Maryland, New York, and Virginia should stop using the product immediately.

SUNGAL
Cyclamate adulteration
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Food & Beverages
HIGH
FDA FOOD

Wang Globalnet Recalls Frozen Oysters Over Norovirus Risk

Wang Globalnet recalled 1,705 cases of frozen oysters on August 7, 2025. The product may be contaminated with Norovirus. The affected oysters were distributed across retail locations in the Northeast and Southwest regions of the U.S.

Wang Globalnet
Oyster product
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Detox Supplement Over Misbranding

Hi-Tech Pharmaceuticals recalled 85,950 units of its Phytoform Fruits & Greens Formula on August 6, 2025. The product contains unapproved drug claims and is misbranded. Consumers should stop using the product immediately and seek a refund.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Slimaglutide Over Misbranding Risk

Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide on August 6, 2025. The recall is due to unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek a refund or replacement.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Joint-RX Supplement Over Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of its Joint-RX dietary supplement on August 6, 2025. The recall occurred due to unapproved drug claims related to the product. Consumers should not consume this supplement and should seek refunds or replacements.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Dietary Supplement Over Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of its Battle Hardener dietary supplement on August 6, 2025. The product makes unapproved drug claims and poses a high health risk. Consumers should stop using the product immediately and contact the company for a refund.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Taurine Supplement Over Misbranding

Hi-Tech Pharmaceuticals recalled 85,950 units of its Taurine Mental & Athletic Performance dietary supplement on August 6, 2025. The company faces scrutiny for unapproved drug claims and misbranding. Consumers are urged to stop using the product immediately.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Fish Oil Recalled Over Unapproved Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of its fish oil soft gels on August 6, 2025, due to unapproved drug claims. The recall affects multiple states across the U.S. Consumers should stop using the product immediately.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

The Candy Barn Recalls Chocolate Fudge Over Allergen Labeling Issue

The Candy Barn recalled 665 packages of its Chocolate Fudge on August 6, 2025. The product does not list egg in the allergen statement, posing a risk to those with egg allergies. Consumers should not consume the product and seek a refund.

The Candy Barn
Allergen labeling:
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Food & Beverages
HIGH
FDA FOOD

Hi-Tech Pharmaceuticals Recalls Uric Acid Control Supplement

Hi-Tech Pharmaceuticals recalled 85,950 units of its dietary supplement on August 6, 2025. The product contains unapproved drug claims, posing potential health risks. Consumers should stop using the supplement and seek refunds immediately.

Hi-Tech Pharmaceuticals
Unapproved Drug
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Food & Beverages
HIGH
FDA FOOD

The Candy Barn Recalls English Toffee Over Allergen Mislabeling

The Candy Barn recalled 665 packages of English Toffee on August 6, 2025. The product contains undeclared pecans, posing a risk to those with tree nut allergies. Consumers should not eat the candy and should seek a refund or replacement.

The Candy Barn
Allergen labeling:
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Food & Beverages
HIGH
FDA FOOD

The Candy Barn Recalls Chocolate Pecan Fudge Over Allergen Risk

The Candy Barn recalled 665 packages of Chocolate Pecan Fudge on August 6, 2025. The product lacks proper allergen labeling for pecans and eggs, posing a high risk to consumers. The recall affects products distributed in Kalona, Iowa.

The Candy Barn
Allergen labeling:
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