These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

2,168 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
Recalled iMirror Rechargeable Electric Fly Swatter
HIGH
CPSC

iMirror Recalls Electric Bug Zapper Due to Fire Hazard

iMirror Inc. recalled its Electric Bug Zapper Racket, Fly Swatter, and Mosquito Swatter on July 24, 2025. The rechargeable battery can catch fire during extended use. Consumers should stop using the products and contact iMirror for a full refund.

iMirror
The rechargeable
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Recalled Transpro A3 Hub Motor Electric Scooter
HIGH
CPSC

Transpro Recalls Electric Scooters Over Fire Risks

Transpro US recalled electric scooters on July 24 due to fire hazards. The A3 Hub Motor, A11F Spark, and R1 Commuter scooters have unauthorized lithium-ion battery certification labels. Consumers should stop using these scooters and contact Transpro for a refund or replacement.

Transpro US
The battery
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Recalled Pura 4 Smart Home Fragrance Diffuser with detachable cover
HIGH
CPSC

Pura Scents Recalls Fragrance Diffusers Over Magnet Ingestion Hazard

Pura Scents recalled detachable covers of its Smart Home Fragrance Diffusers on July 24, 2025. The covers contain magnets that can detach and pose an ingestion hazard to children. Consumers should stop using the product immediately and contact Pura Scents for a replacement.

Pura Scents
The magnets
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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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA 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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HIGHFDA DEVICE

DJO Surgical Recalls Glenoid Reamer Sleeve Due to Kickback Risk

DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.

DJO Surgical
Their is
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