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

3,615 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
Health & Personal Care
HIGH
FDA DEVICE

Abbott Recalls FreeStyle Libre 3 Plus Sensors Over Low Glucose Risk

Abbott Diabetes Care recalled 1,663,241 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may lead to incorrect low glucose results, creating serious health risks for users. Patients should stop using the sensors immediately and follow recall instructions.

Abbott Diabetes Care
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Abbott Recalls FreeStyle Libre 3 Plus Sensor Over Glucose Errors

Abbott Diabetes Care recalled 8,062 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may cause inaccurate low glucose readings, posing serious health risks. Consumers should stop using the device immediately and follow recall instructions.

Abbott Diabetes Care
Due to
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Health & Personal Care
HIGH
FDA DEVICE

LotFancy Urinary Tract Infection Test Strips Recalled for False Results

LotFancy recalled 91,366 urinary tract infection test strips on November 22, 2025. The strips may produce false results, risking inappropriate medical intervention. Affected products include various models sold nationwide in states like Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks

Changchun Wancheng Bio-Electron Co. recalled 32,500 Keto-pH-Uric Acid Test Strips on November 22, 2025. The strips may provide inaccurate results and lead to inappropriate medical intervention. The recall affects products distributed nationwide in Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Recalls Ovulation Test Over False Results Risk

Changchun Wancheng Bio-Electron Co. recalled 1,000 LH One Step Ovulation Test Devices on November 22, 2025. The tests may deliver false or inaccurate results, potentially leading to inappropriate medical intervention. The recall affects U.S. consumers in Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Food & Beverages
HIGH
FDA FOOD

Wegmans Grated Cheese Recalled Over Listeria Contamination

Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.

Wegmans Food Markets
Product may
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Food & Beverages
HIGH
FDA FOOD

GBC Food Services Recalls Chicken Caesar Salad Over Listeria Risk

GBC Food Services recalled EverRoast Chicken Caesar Salad on November 22, 2025, due to potential Listeria monocytogenes contamination. The recall affects 2 units of the product distributed in Kentucky and Indiana. Consumers should not consume this product and seek a refund or replacement.

GBC Food Services
Potential presence
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Food & Beverages
HIGH
FDA FOOD

GBC Food Services Recalls Chicken Caesar Wrap for Listeria Risk

GBC Food Services recalled 11 units of EverRoast Chicken Caesar Wrap on November 22, 2025. The recall occurred due to potential contamination with Listeria monocytogenes. The affected products were distributed in Kentucky and Indiana.

GBC Food Services
Potential presence
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Bio-Electron Recalls Diagnostic Test Strips

Changchun Wancheng Bio-Electron Co. recalled 1,000 units of S. Typhi/Para Typhi A Antigen test strips on November 22, 2025. The recall affects tests distributed nationwide, which may produce false results and lead to inappropriate medical intervention.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Bio-Electron Recalls Menopause Test Cassette

Changchun Wancheng Bio-Electron Co. recalled 1,000 Menopause Test Cassettes on November 22, 2025. The recall follows reports that the devices can produce false or inaccurate results, potentially leading to inappropriate medical interventions. Customers in Texas, Georgia, and California should stop using the test immediately and follow recall instructions.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Vivoo Vaginal pH Test Recalled Over Inaccurate Results Risk

Vivoo recalled 3,000 vaginal pH tests on November 22, 2025. The tests may cause false results leading to inappropriate medical interventions. The products were distributed nationwide, including Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Vivoo Test Strips Recalled Due to False Diagnostic Risk

Changchun Wancheng Bio-Electron Co. recalled 3,300 Vivoo test strips on November 22, 2025. The devices may provide inaccurate results, leading to inappropriate medical actions. Affected products include sodium, Vitamin C, and hydration tests.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Bio-Electron Recalls Vivoo pH Test for Inaccurate Results

Changchun Wancheng Bio-Electron Co. recalled 500 Vivoo pH Test strips on November 22, 2025. The recall follows concerns over false diagnostic results that could lead to inappropriate medical interventions. These devices were distributed nationwide, including Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Recalls Male Fertility Test Over False Results

Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Recalls Male Fertility Test Over Inaccurate Results

Changchun Wancheng Bio-Electron Co. recalled 4,800 Exploro Male Fertility Tests on November 22, 2025. These devices may provide false diagnostic results, potentially leading to inappropriate medical interventions. Consumers should stop using the product immediately and follow recall instructions.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Over False Results

Changchun Wancheng Bio-Electron Co. recalled 500 Vivoo Protein Test strips on November 22, 2025. The devices may provide false diagnostic results, leading to inappropriate medical interventions. This recall affects consumers nationwide in Texas, Georgia, and California.

Changchun Wancheng Bio-Electron Co.
Test strips
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Pharmaceuticals Recalls Bisoprolol Tablets Due to Contamination

Glenmark Pharmaceuticals recalled over 11,000 bottles of Bisoprolol Fumarate and Hydrochlorothiazide Tablets on November 21, 2025. Testing revealed traces of ezetimibe, posing a health risk. Consumers should stop using the product immediately and contact their healthcare provider.

BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE
Cross Contamination
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Food & Beverages
HIGH
FDA FOOD

Lotus Mom Corporation Recalls Brass Tope Due to Lead Contamination

Lotus Mom Corporation recalled 10 units of Brass Tope on November 21, 2025, due to potential contamination with leachable lead. Consumers should not use the product and seek refunds or replacements. The recall affects distribution in California and Colorado.

Lotus Mom Corporation dba Indian Kitchen Mart
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Ambriola Grated Pecorino Romano Recalled Due to Listeria Risk

Ambriola Co., Inc. recalled 6,632 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a dangerous bacteria that can cause serious illness. Consumers should not consume the affected product and should seek refunds or replacements.

Ambriola Co., Inc.
Product tested
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