chemical hazard Recalls

1,035 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DRUG

DermaRite Recalls KleenFoam Soap Over Microbial Contamination

DermaRite Industries recalled 6,973 cartridges of KleenFoam Antimicrobial Foam Soap on July 17, 2025. The product contains a harmful bacterial contamination, Burkholderia cepacia. Consumers should stop using the soap immediately and seek guidance from healthcare providers.

KLEENFOAM
Microbial Contamination
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Health & Personal Care
HIGH
FDA DRUG

DermaKleen Antiseptic Lotion Soap Recalled for Microbial Contamination

DermaRite Industries LLC recalled 11,321 bags of DermaKleen antiseptic lotion soap on July 17, 2025. The product, contaminated with Burkholderia cepacia, poses a serious health risk. Consumers should stop using the product immediately and contact health providers for guidance.

DERMAKLEEN
Microbial Contamination
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Recalls Semaglutide Injection for Low Potency

Boothwyn Pharmacy recalled 186 vials of Semaglutide, 2.5 mg/mL injection on July 9, 2025. The product is subpotent and poses a risk to consumers. Healthcare providers and consumers should stop using this product immediately.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Recalls Semaglutide Injection for Subpotency

Boothwyn Pharmacy recalled 642 vials of Semaglutide injection on July 9, 2025. The recall follows the discovery that the drug is subpotent. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Boothwyn Pharmacy Recalls Fluorescein 2% Ophthalmic Solution

Boothwyn Pharmacy recalled 8 vials of Fluorescein 2% Ophthalmic Solution on July 9, 2025. The recall occurred due to the drug being subpotent, posing potential health risks. Consumers should stop using the product immediately and seek guidance from their healthcare provider.

Boothwyn Pharmacy
Subpotent Drug
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Health & Personal Care
HIGH
FDA DRUG

Rite Aid Recalls Alcohol Prep Pads Due to Subpotency Hazard

Rite Aid recalled 984,000 first aid alcohol prep pads on July 7, 2025, due to subpotent isopropyl alcohol levels. The affected product may not effectively disinfect, posing health risks to users.

Rite Aid Corporation
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

Walmart Recalls ReliOn Alcohol Swabs for Subpotency Risk

Walmart recalled 3.46 million ReliOn Sterile Alcohol Swabs on July 7, 2025. The swabs contain isopropyl alcohol levels below the labeled concentration. Consumers should stop using the product immediately.

Walmart
Subpotent Drug-
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Health & Personal Care
HIGH
FDA DRUG

Medline Alcohol Prep Pads Recalled Due to Subpotent Alcohol Levels

Medline Industries recalled approximately 6.67 million alcohol prep pads on July 7, 2025. The recall stems from isopropyl alcohol levels falling below the labeled concentration. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Medline Alcohol Prep
Subpotent Drug-
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Food & Beverages
HIGH
FDA FOOD

Evergreen Orchard Farm Korean Pear Juice Recalled Over Safety Issues

Evergreen Orchard Farm recalled 610 cases of Korean Pear Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The affected product was distributed to Pennsylvania, New Jersey, and New York. Consumers should not consume this juice and are advised to seek refunds or replacements.

Evergreen Orchard Farm
Lack of
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Food & Beverages
HIGH
FDA FOOD

Evergreen Farm Jujube Juice Recalled Over Safety Concerns

Evergreen Orchard Farm recalled 197 cases of Jujube Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The juice was distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds immediately.

Evergreen Orchard Farm
Lack of
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Food & Beverages
HIGH
FDA FOOD

CHETAK NEW YORK Recalls Sprouted Mat Due to Salmonella Risk

CHETAK NEW YORK recalled 5,232 packets of Deep Sprouted Mat on June 28, 2025. The product tested positive for Salmonella, a serious health risk. Consumers in CA, NJ, IL, FL, and TX should not consume the product and seek refunds.

CHETAK NEW YORK
Product tested
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Health & Personal Care
HIGH
FDA DEVICE

bioMerieux Recalls VITEK 2 AST Test Kits Over False Resistance Risk

bioMerieux recalled 235,269 VITEK 2 Gram-negative AST Test Kits on June 26, 2025. The recall follows potential false resistant results for Colistin with specific bacteria. This may affect patient treatment decisions in multiple countries.

bioMerieux
Potential for
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Food & Beverages
HIGH
FDA FOOD

BulkSupplements.com Inositol Powder Recalled Due to Contamination

BulkSupplements.com recalled 1,001 units of Inositol powder on June 25, 2025, due to potential contamination with Staphylococcus aureus. The recalled products include 250g, 500g, and 1kg packages sold in the U.S. and several international locations.

BulkSupplements.com
Finished product
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