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

2,775 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
Food & Beverages
HIGH
FDA FOOD

Wegmans Camembert Cheese Recalled Due to Listeria Risk

Wegmans Food Markets recalled 4,884 units of Medium Camembert Soft Ripened Cheese on August 12, 2025. The product may be contaminated with Listeria monocytogenes, posing a serious health risk. Consumers should not eat the cheese and should contact the company for refunds.

Wegmans Food Markets
Products may
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Food & Beverages
HIGH
FDA FOOD

Wegmans Grilling Camembert Recalled Due to Listeria Risk

Wegmans Food Markets recalled 4,884 units of Grilling Camembert on August 12, 2025, due to possible contamination with Listeria monocytogenes. The affected products are packaged in black and gold metal trays and distributed in several states including New York and Pennsylvania. Consumers should not consume this product and seek a refund or replacement.

Wegmans Food Markets
Products may
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Health & Personal Care
HIGH
FDA DRUG

Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)

Viona Pharmaceuticals recalls Tavaborole Topical Solution 5% 10 mL bottles, distributed nationwide in the U.S. The effective recall date is August 12, 2025. The product is manufactured by Zydus Lifesciences Ltd. Discoloration was cited as the reason for the recall. Consumers should stop using the product and contact the distributor for guidance.

TAVABOROLE
Discoloration
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Food & Beverages
HIGH
FDA FOOD

Wegmans Cheese Flight Recalled Due to Listeria Contamination

Wegmans Food Markets recalled 4,884 units of its Assorted Cheese Flight on August 12, 2025. The product may be contaminated with Listeria monocytogenes, a serious foodborne pathogen. The recall affects consumers in NY, PA, MA, NJ, MD, VA, NC, DE, CT, and DC.

Wegmans Food Markets
Products may
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Health & Personal Care
HIGH
FDA DEVICE

Max Mobility/Permobil Recalls 8,413 Smart Drive MX2+ SpeedControl Dials (2025)

Max Mobility LLC recalls 8,413 Smart Drive MX2+ SpeedControl Dials used with the SmartDrive MX2+ Wheelchair Power Assist. A faulty electrical connection between the dial and the motor can cause loss of control. Stop using the device immediately and follow recall letters for instructions.

Max Mobility
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall 840 Units (2025)

Applied Medical Technology recalled 840 NutraGlide ENFit nasal feeding tubes distributed in the United States to Massachusetts and Rhode Island. The tubes have distal tips that may detach at lower than expected forces. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Applied Medical Technology
The nasal
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Health & Personal Care
HIGH
FDA DEVICE

Agilent Technologies Denmark ApS Recalls 67 FLEX CD20 Antibody for Potential Weak Staining

Agilent Technologies Denmark ApS recalled 67 FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use antibodies sold nationwide in the United States. The antibody may stain weakly, potentially producing false negative CD20 results. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.

Agilent Technologies Denmark ApS
Their is
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Health & Personal Care
HIGH
FDA DRUG

Lannett Lisdexamfetamine Recall Alerts 40 mg Capsules for Label Mix-Up (2025)

Lannett Company, Inc. recalls 8,544 bottles of Lisdexamfetamine Dimesylate 40 mg capsules distributed nationwide. A labeling mix-up may have placed 30 mg and 40 mg strengths in mislabeled bottles. Healthcare providers and patients should stop use and contact the company for guidance.

Lisdexamfetamine Dimesylate
Labeling: Label
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Health & Personal Care
HIGH
FDA DEVICE

Agilent Technologies Recalls 65 FLEX Monoclonal CD20 Antibodies Over Weak Staining Risk (GA60461-2CN

Agilent Technologies recalled 65 FLEX Monoclonal Mouse Anti-Human CD20cy antibodies distributed nationwide in the United States. The recall cites weak staining that may yield false negative CD20 results. Labs and healthcare providers should stop using the product immediately and follow the manufacturer’s recall instructions.

Agilent Technologies Denmark
Their is
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Health & Personal Care
HIGH
FDA DEVICE

Agilent FLEX Monoclonal CD20 Antibody Recalled for 4,145 Units (2025)

Agilent Technologies Denmark ApS recalled 4,145 FLEX Monoclonal Mouse Anti-Human CD20cy, Clone L26, Ready-to-Use antibodies distributed nationwide in the United States. The defect is a potential for weak staining that can yield a false negative CD20 result. Labs should stop using the product immediately and follow manufacturer recall instructions.

Agilent Technologies
Their is
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Food & Beverages
HIGH
FDA FOOD

SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)

SUNGAL Inc. recalls 29 cases of UDK Half Plum, 170 g containers distributed to California, Maryland, New York and Virginia. The product is adulterated with cyclamate. Consumers should not consume it and should email SUNGAL Inc. for refund or replacement information.

SUNGAL
Cyclamate adulteration
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Health & Personal Care
HIGH
FDA DEVICE

PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide

Philips Medical Systems Nederland B.V. recalls four IntelliSpace Cardiovascular software units distributed to facilities in Georgia, North Carolina and Texas. A software issue can display outdated information on the device. Hospitals should stop using the device immediately and follow Philips recall instructions.

Philips Medical Systems Nederland B.V.
Software issue
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