glass Recalls

51 recalls tagged with “glass”.

Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Icosapent Ethyl Capsules Over Subpotency

Zydus Pharmaceuticals recalled 22,896 bottles of Icosapent Ethyl capsules on December 30, 2025. The recall stems from leakage and oxidation that may reduce the drug's effectiveness. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Zydus Pharmaceuticals
Subpotent Drug:
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Health & Personal Care
HIGH
FDA DRUG

Aleve 60-Count Pain Relievers Recalled for CGMP Deviations by Gold Star Distribution (2026)

Gold Star Distribution recalls Aleve 60-count pain relievers distributed nationwide due to CGMP deviations and insanitary conditions at its distribution center. Rodent exposure and activity were reported at the facility. Consumers and healthcare providers should stop using the product immediately and contact Gold Star Distribution for guidance.

Aleve
CGMP Deviations:
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Food & Beverages
HIGH
FDA DRUG

Swan White Clear Alcohol Recall by Gold Star Distribution in 2026

Gold Star Distribution recalls Swan White Clear Alcohol, 50% ABV, 16 oz, 12 count, nationwide. FDA enforcement cites CGMP deviations and insanitary distribution-center conditions including rodent exposure. Stop using the product now and contact the distributor or a healthcare provider for guidance.

Swan
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DRUG

Imprimis NJOF Recalls Intraocular Injection Over Glass Particles

Imprimis NJOF, LLC recalled 314 boxes of Tri-Moxi+¿ intraocular injections on December 18, 2025. The recall is due to the presence of glass-like particles in the product. Consumers and healthcare providers should stop using the product immediately and contact the company for further guidance.

Imprimis NJOF
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)

Nivagen Zinc Oxide Ointment 20% skin protectant, manufactured in India for Nivagen Pharmaceuticals and distributed nationwide in the USA, is recalled. The recall covers 912 containers. The defect cited is cGMP deviations. Consumers and healthcare providers should stop using the product and follow guidance from Blossom Pharmaceuticals or a healthcare professional.

Nivagen Zinc Oxide
cGMP deviations
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Food & Beverages
HIGH
FDA FOOD

Sno Pac Foods Recalls Frozen Spinach Due to Listeria Risk

Sno Pac Foods recalled 4,006 cases of frozen organic spinach on October 6, 2025, due to potential Listeria contamination. Affected products include various lot codes with best-by dates ranging from April to July 2027. Consumers should not eat this product and seek refunds immediately.

SNO PAC FOODS
Organic Spinach
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Food & Beverages
HIGH
FDA FOOD

New Age International Recalls Enoki Mushroom Over Listeria Risk

New Age International, Inc. recalled 175 boxes of its Signature brand Enoki Mushroom on September 29, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not eat the product and seek a refund or replacement.

New Age International
Product may
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Food & Beverages
HIGH
FDA FOOD

Kroger Recalls Basil Pesto Bowtie Pasta Salad Over Listeria Risk

Kroger recalled 5,567.4 pounds of Basil Pesto Bowtie Pasta Salad on September 26, 2025. The salad contains a pasta ingredient linked to potential Listeria monocytogenes contamination. Affected products were sold in various states across the U.S.

The Kroger Co
Store-made deli
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Food & Beverages
HIGH
FDA FOOD

Toto Foods Recalls S'Mores Cookies Over Soy Allergy Risk

Toto Foods recalled 120,180 units of S'Mores Ooey Gooey Cookies on August 20, 2025. The product label conflicts regarding soy content pose a health risk to consumers with soy allergies. The cookies were distributed across 13 states including California and New York.

Toto Foods
Product label
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