immediate action Recalls

2,715 recalls tagged with “immediate action”.

Recalled Apollo Electric Scooter
MEDIUM
CPSC

Apollo Recalls Electric Scooters Over Fall Hazard

Apollo recalled certain electric scooters on July 24, 2025, due to a welding defect. The defect can cause the stem to break, leading to falls and injuries. Consumers should stop using the scooters and contact Apollo for a free replacement.

Apollo
The weld
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Recalled LIVACTI Retractable Safety Gate - Black
HIGH
CPSC

LIVACTI Safety Gates Recalled Due to Entrapment Risk

LIVACTI recalled retractable safety gates on July 24, 2025, due to serious entrapment hazards. The gates can pose a risk of injury or death to children. Consumers should stop using them immediately and seek refunds.

LIVACTI
The recalled
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalls Cashew Coffee Milk Over Pathogen Risk

Everpress Juice recalled cashew coffee milk on July 24, 2025, due to potential contamination with pathogenic bacteria. The product poses a high risk to consumers' health. Distribution included multiple states across the U.S.

Everpress Juice
Under-processed product
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalls DETOX GREENS Over Pathogen Risk

Everpress Juice recalled its DETOX GREENS product on July 24, 2025, due to potential contamination with pathogenic bacteria. Consumers in 20 states should not consume the product. No injuries have been reported, but the health risk is significant.

Everpress Juice
Under-processed product
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter MicroScan Neg MIC 56 Panels Recalled for Contamination Risk (2026)

Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.

Beckman Coulter
Due to
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalls Cashew Milk Over Pathogenic Bacteria Risk

Everpress Juice recalled its cashew milk on July 24, 2025, due to under-processing that may lead to pathogenic bacteria contamination. The recall affects consumers in 15 states, posing a high health risk. Consumers should stop using the product immediately and seek a refund or replacement.

Everpress Juice
Under-processed product
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalls Sweet Greens Juice Over Bacterial Contamination

Everpress Juice recalled its Sweet Greens product on July 24, 2025, due to possible pathogenic bacteria. The under-processed juice poses a high risk to human health. The recall affects distribution in multiple states, including California and Texas.

Everpress Juice
Under-processed product
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Spicy Lemonade Recall Due to Pathogenic Bacteria

Everpress Juice recalled spicy lemonade on July 24, 2025, due to under-processing that may lead to harmful bacteria. This recall affects consumers in 14 states including California and Texas. The product poses a high health risk and should not be consumed.

Everpress Juice
Under-processed product
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalled for Potential Bacterial Contamination

Everpress Juice recalled its upbeat product on July 24, 2025, due to under-processing potentially exposing consumers to pathogenic bacteria. The recall affects consumers across 15 states, including California and Texas. No injuries or illnesses have been reported, but the risk remains high.

Everpress Juice
Under-processed product
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Food & Beverages
HIGH
FDA FOOD

Everpress Juice Recalls Pineapple Mint Juice Over Bacterial Risk

Everpress Juice recalled Pineapple Mint Juice on July 24, 2025, due to potential contamination with pathogenic bacteria. This under-processed product poses a serious health risk to consumers. The recall affects multiple states including California and Texas.

Everpress Juice
Under-processed product
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Health & Personal Care
HIGH
FDA DRUG

Taizhou Kangping Medical Recalls Antiseptic Towelettes for Sterility Issues

Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.

Taizhou Kangping Medical Science And Technology Co.
Lack of
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Health & Personal Care
HIGH
FDA DRUG

AUM Pharmaceuticals Recalls Alcohol Prep Pads Due to cGMP Deviations

AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.

YANGZHOU YULOU PAPER PRODUCTS CO.
cGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Merck Recalls Belsomra Tablets Due to Dissolution Issues

Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets on July 21, 2025. The recall stems from a failure in dissolution specifications that could delay drug release. Consumers should stop using the product immediately and consult healthcare providers for guidance.

BELSOMRA
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Middlefield Cheese Recalled Due to Listeria Contamination Risk

Middlefield Original Cheese Cooperative recalled 640 pounds of cheese on July 21, 2025. The recall affects Monterey Jack and Farmers Cheese due to potential Listeria monocytogenes contamination. The products were distributed in Kentucky, Ohio, and Pennsylvania.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Cheese Recalled Due to Listeria Contamination Risk

Middlefield Original Cheese Co-op recalled 246.5 pounds of 100% Grass-Fed Pepper Jack Cheese on July 21, 2025. The cheese may be contaminated with Listeria monocytogenes, which can cause serious illness. Consumers should not eat this product and seek a refund.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

Summa Therapeutics Recalls 22 Finesse BTK Multicath Angioplasty Balloons Over Burst Specifications (

Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.

Finesse BTK Multicath
Potential for
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