Critical Food Safety Alert: Check your refrigerator and pantry immediately. 2 high-risk food recalls reported in the last 30 days.
Real-time monitoring of 527 food safety recalls and ongoing outbreak investigations. Track contaminated products, multi-state outbreaks, and FDA/CDC alerts including Listeria, Salmonella, and E. coli.
CDC and FDA are investigating multiple active foodborne illness outbreaks. Check the recalls below for affected products and retailers. Deaths and hospitalizations have been reported.
Boar's Head recalled 405 bags of Pecorino Romano Grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health risk. Consumers should not consume the cheese and seek a refund or replacement immediately.
Ambriola Co., Inc. recalled 184 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria that can cause serious illness. Consumers in multiple states should not consume this product.
Ambriola Co., Inc. recalled 964 bags of Grated Pecorino Romano on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health threat. Affected states include AZ, CA, CO, and more.
Potential contamination with leachable lead.
Potential contamination with leachable lead.
Potential contamination with leachable lead.
Potential contamination with leachable lead.
Doughy brand recalled 113 units of Chocolate Chip Cookie Dough on November 20, 2025. The product may be contaminated with Salmonella. Consumers should stop using the product immediately.
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, LLC recalled 278 bottles of Boswellia Herbal Supplement on November 20, 2025. The product has unapproved drug claims and lacks a Supplement Facts label. Consumers should stop using it immediately and seek a refund.
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 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, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately and seek a refund.
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 recalled 48 bags of Organic Ginger Root Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume the product and seek a refund.
A New Life Herbs recalled 275 bottles of Pain Away Herbal Supplement on November 20, 2025. The product contains unapproved drug claims and lacks a Supplement Facts label. Consumers should not consume this product and seek refunds.
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.
Sonex recalled two aluminum pots on November 19, 2025, due to leachable lead levels of 0.323mg/L. The recall affects products distributed in New York. Consumers must stop using the product and seek refunds or replacements.
GUSTO GROUP recalled 7 cases of DPA161 Shrimp Paste on November 19, 2025. Testing revealed elevated lead levels in the product. Consumers in Iowa and New Jersey should not consume this product.
GUSTO GROUP, INC. recalled 7 cases of Shrimp Paste (Klong Kone) 'M' due to high lead levels. The recall affects products distributed in Iowa and New Jersey. Consumers should not consume the product and seek refunds immediately.
New Way Import Inc recalled preserved mustard on November 19, 2025, due to undeclared wheat allergens. The product, sold in predominantly green packaging with black Chinese lettering, poses a high risk to consumers with wheat allergies. Approximately 55 cases of the product were distributed to 23 retail locations in California.
JR Simplot Company recalled 7,053 cases of Traditional Reduced Sodium Tater Gems on November 18, 2025. The recall is due to plastic fragments embedded in the product, posing a choking hazard. Consumers in 15 states are advised not to consume the affected items.
Karabetian Import and Distribution recalled 338 boxes of Zimi Puff Pastry on November 18, 2025. The recall was initiated due to the presence of partially hydrogenated oils, which are not permitted in foods exported to the U.S. Consumers should not consume the product and seek a refund or replacement.
Karabetian Import and Distribution recalled 338 boxes of Zimi Kunefe on November 18, 2025, due to partially hydrogenated oils. The recall affects frozen dessert products distributed in nine states including California and Texas.
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