chemical hazard Recalls

1,003 recalls tagged with “chemical hazard”.

Food & Beverages
HIGH
FDA FOOD

GUSTO GROUP Recalls Shrimp Paste Over High Lead Levels

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.

GUSTO GROUP
Product tested
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Food & Beverages
HIGH
FDA FOOD

New Way Import Recalls Mustard Over Undeclared Wheat Allergen

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.

NEW WAY IMPORT
Undeclared allergen
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Food & Beverages
HIGH
FDA FOOD

Sonex Aluminum Pot Recall: 2 Units for Lead Leaching (2025)

Two Sonex aluminum pots sold in New York are recalled after tests found leachable lead at 0.323 mg/L. The recall is issued by Alanwar Food Corp. Consumers who own the pots should not use them for cooking and should contact Alanwar Food Corp. for refund or replacement information.

Sonex
Products found
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Food & Beverages
HIGH
FDA FOOD

Zimi Puff Pastry Recalled Due to Partially Hydrogenated Oils

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
partially hydrogenated
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Food & Beverages
HIGH
FDA FOOD

Karabetian Import and Distribution Recalls Frozen Kunefe for PHOs

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.

Karabetian Import and Distribution
partially hydrogenated
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Nebivolol Tablets Over Contamination

Glenmark Pharmaceuticals recalled 672 bottles of Nebivolol Tablets on November 18, 2025, due to cross-contamination. The 20 mg tablets, prescribed for hypertension, may pose health risks. Consumers should stop using the product and seek guidance from healthcare providers.

NEBIVOLOL
Cross Contamination
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Food & Beverages
HIGH
FDA FOOD

JR Simplot Recalls Tater Gems Due to Plastic Fragments

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.

JR Simplot
Plastic fragments.
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Health & Personal Care
HIGH
FDA DEVICE

Sheathing Technologies Recalls Ultrasound Probe Covers Over Infection Risk

Sheathing Technologies recalled 12 units of its ultrasound probe covers on November 17, 2025, due to potential contamination risks. The non-sterile vaginal and rectal covers may have defects that pose an infection risk during use. Consumers should stop using the product immediately and follow the manufacturer's instructions.

Sheathing Technologies
Vaginal/rectal ultrasound
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Food & Beverages
HIGH
FDA FOOD

Venzu Traders Recalls Cinnamon Powder Over Lead Contamination

Venzu Traders LLC recalled 24 cases of cinnamon powder on November 14, 2025, due to potential lead contamination. The affected product weighs 3.5 ounces and is sold under UPC 7 46241 29537 8. Consumers should stop using this product immediately and contact the distributor for a refund.

VENZU TRADERS
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Cipla Recalls Cinacalcet Hydrochloride Tablets Over Impurity Risk

Cipla USA, Inc. recalled 63,504 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall results from a nitrosamine impurity, N-nitroso-cinacalcet, exceeding acceptable daily intake limits. Consumers should stop using the tablets immediately and contact healthcare providers for guidance.

CINACALCET
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Recalls Cinacalcet Hydrochloride Tablets Over Nitrosamine Hazard

Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.

CINACALCET
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Recalls Cinacalcet Hydrochloride Tablets Over Impurity Risk

Cipla USA recalled 12,576 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025, due to a nitrosamine impurity. The impurity, N-nitroso-cinacalcet, exceeds acceptable daily intake limits. Consumers must stop using this product immediately and contact healthcare providers for guidance.

CINACALCET
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Lupin Pharmaceuticals Recalls Ganirelix Acetate Injection for Impurity Risk

Lupin Pharmaceuticals recalled 32,736 vials of Ganirelix Acetate Injection on November 13, 2025. The recall follows the discovery of impurities in the drug. Consumers and healthcare providers should stop using the product immediately to avoid health risks.

GANIRELIX ACETATE
Failed impurities/degradation
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Food & Beverages
HIGH
FDA FOOD

Stuffed Foods Recalls Cacio e Pepe Arancini Over Soy Allergy Risk

Stuffed Foods recalled 51 cases of Cacio e Pepe Arancini on November 12, 2025. The products contain undeclared soy protein concentrate, posing a risk to those with soy allergies. The affected items were distributed in Connecticut, Massachusetts, Florida, and Missouri.

Stuffed Foods
Undeclared Soy
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Food & Beverages
HIGH
FDA FOOD

Santos Agency Recalls Brass Langri Cookware Over Lead Risk

Santos Agency recalled Brass Langri Cookware on November 12, 2025, due to potential lead contamination. Consumers should not use the product and seek a refund. The affected item features sticker label: 14.

Santos Agency
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health Recalls ChemoPlus Gowns Over Expiration Date Error

Cardinal Health 200 recalled 251,165 ChemoPlus gowns on November 12, 2025, due to incorrect expiration dates. The gowns are mislabeled with a five-year shelf life instead of the correct three years. Patients and healthcare providers must stop using these gowns immediately.

Cardinal Health 200
Affected gowns
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Health & Personal Care
HIGH
FDA DRUG

Dr. Reddy's Labs Recalls Varenicline Tablets Over Potency Issues

Dr. Reddy's Laboratories recalled 4,800 bottles of Varenicline tablets on November 11, 2025, due to sub potent drug levels. The affected lot failed stability tests, posing potential health risks to users. Consumers should stop using the product immediately and consult healthcare providers.

VARENICLINE TARTRATE
Sub potent
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