1,035 recalls tagged with “chemical hazard”.
Domino Foods, Inc. recalled 4,500 bags of granulated sugar on August 12, 2025. The recall stems from potential contamination with foreign objects. The affected products were distributed in California and Utah.
Applied Medical Technology recalled 200 NutraGlide Nasal Feeding Tubes on August 12, 2025. The distal tips may detach under lower than expected forces, posing a risk to patients. This recall affects devices distributed in Massachusetts and Rhode Island.
Lannett Company recalled 8,544 bottles of Lisdexamfetamine Dimesylate Capsules on August 11, 2025. The recall occurred due to a labeling mix-up where 40 mg capsules were mislabeled as 30 mg. This issue poses a high risk to consumers who may receive incorrect dosages.
Agilent Technologies Denmark ApS recalled 65 units of its FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26 on August 11, 2025. The recall stems from potential weak staining that could lead to false negative CD20 identification. Healthcare providers and patients should stop using the product immediately.
Quallent Pharmaceuticals recalled 3,591 bottles of Duloxetine Delayed-Release Capsules on August 8, 2025. The recall stems from CGMP deviations regarding an impurity exceeding safety limits. Consumers should stop using the product immediately and contact their healthcare provider.
Glenmark Pharmaceuticals Inc. recalled 22,656 bottles of Theophylline extended-release tablets on August 8, 2025. The recall follows reports of failed dissolution specifications that could impact medication efficacy. Consumers should stop using the product and consult healthcare providers immediately.
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.
Medline Industries recalled 88 units of its Sterile Convenience Kits on August 8, 2025. The kits were labeled as sterile but did not undergo the required sterilization process. Healthcare providers and patients must stop using these kits immediately.
Medline Industries recalled 22 sterile convenience kits on August 8, 2025, after discovering they had not been sterilized. The affected models include DYNJ0382730O and DYNJ61038B. This recall impacts states including Florida, Maryland, New Jersey, and Tennessee.
Monica Vinader recalled select 14k Yellow Gold Mini Heart Chain Bracelets, Necklaces, and Stud Earrings on August 7, 2025. The products contain high levels of cadmium, posing health risks. Consumers should stop using the items immediately and contact the company for a refund or replacement.
Glenmark Pharmaceuticals recalled 6,432 bottles of Carvedilol Tablets on August 7, 2025. The recall stems from CGMP deviations due to the presence of a nitrosamine impurity above acceptable levels. Consumers should stop using the product immediately and contact healthcare providers for guidance.
Glenmark Pharmaceuticals recalled 4,800 bottles of Carvedilol Tablets on August 7, 2025. The recall stems from CGMP deviations leading to high levels of nitrosamine impurities. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Glenmark Pharmaceuticals recalled 44,328 bottles of Carvedilol Tablets, USP, 3.125 mg on August 7, 2025. The recall follows the discovery of N-Nitroso Carvedilol I impurity above acceptable levels. Consumers should stop using this medication immediately and consult their healthcare providers.
Guangzhou Ariel Biotech recalled Séfralls Hair Generation Serum on August 7, 2025. The recall affects an unknown number of units due to the product's non-compliance with child-resistant packaging standards. The defective packaging poses a serious poisoning risk to children if ingested.
The Candy Barn recalled 665 packages of Grandma's Old-Fashioned Peanut Brittle on August 6, 2025. The packaging failed to list peanuts and milk as allergens. Consumers should avoid the product and seek a refund.
The Candy Barn recalled 665 packages of Chocolate Walnut Fudge on August 6, 2025. The product does not list walnut and egg allergens in the 'contains' statement. Consumers should not consume the fudge and seek refunds or replacements.
The Candy Barn recalled 665 packages of Peanut Butter Fudge on August 6, 2025. The product contains undeclared egg allergens not listed in the labeling. Consumers should not consume this fudge and seek a refund or replacement.
The Candy Barn recalled 665 packages of Maple Nut Fudge on August 6, 2025. The product contains undeclared allergens: pecans and eggs. Consumers should not consume the fudge and seek refunds.
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 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.