immediate action Recalls

2,756 recalls tagged with “immediate action”.

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 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 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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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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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

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 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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Food & Beverages
HIGH
FDA FOOD

Ambriola Co. Recalls Pecorino Romano Cheese Over Listeria Risk

Ambriola Co., Inc. recalled 1,015 bags of Sam's Pecorino Romano grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria. Consumers should not consume the product and seek a refund or replacement immediately.

Ambriola Co., Inc.
Product tested
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Oxygen Masks Due to Tubing Disconnect Risk

Medline Industries recalled over 1.6 million oxygen masks on November 21, 2025. The recall affects multiple models after reports of tubing disconnecting during use. This defect can delay patient care and lead to shortness of breath, requiring medical intervention.

Medline Industries, LP
Firm received
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Health & Personal Care
HIGH
FDA DEVICE

Roche Diagnostics Recalling Anti-TSHR Immunoassay Over Diagnosis Risk

Roche Diagnostics Operations recalled 1,300 Anti-TSHR immunoassay cassettes on November 21, 2025. Variability in results may lead to incorrect diagnoses and treatment delays. The recall affects multiple states across the U.S.

Roche Diagnostics Operations
Issues identified:
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Food & Beverages
HIGH
FDA FOOD

SB FOOD Recalls Gummy Candy Over Unallowed Color Additive

SB FOOD recalled 100 cases of Yoyo Gummy Assorted Flavor on November 21, 2025. The product contains an unapproved color, Carmoisine (E122), posing health risks. Consumers should not consume the candy and seek refunds.

SB FOOD
The products
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Food & Beverages
HIGH
FDA FOOD

Boar's Head Grated Cheese Recalled Due to Listeria Risk

Boar's Head recalled 405 bags of Pecorino Romano Grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health risk. Consumers should not consume the cheese and seek a refund or replacement immediately.

Boar's Head
Product tested
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Food & Beverages
HIGH
FDA FOOD

Ambriola Grated Pecorino Romano Cheese Recalled for Listeria Risk

Ambriola Co., Inc. recalled 184 units of Grated Pecorino Romano cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a harmful bacteria that can cause serious illness. Consumers in multiple states should not consume this product.

Ambriola Co., Inc.
Product tested
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Health & Personal Care
HIGH
FDA DEVICE

Fresenius Kabi Recalls Ivenix Infusion System Software Over Safety Issues

Fresenius Kabi USA recalled 30 units of the Ivenix Infusion System LVP Software on November 21, 2025. The recall addresses concerns related to programming instructions for LVP duration. Patients and healthcare providers must stop using the device immediately.

Fresenius Kabi USA
Emphasizing instructions
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Food & Beverages
HIGH
FDA FOOD

SB FOOD Recalls Gummy Candy Over Unallowed Color Additive

SB FOOD recalled 100 cases of Yoyo Gummy Grape Plus Flavor on November 21, 2025. The products contain an unapproved color additive, Carmoisine (E122). The recall affects consumers in 14 states, including New York and Texas.

SB FOOD
The products
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Food & Beverages
HIGH
FDA FOOD

Silvestri Sweets Recalls Cookie Butter Bark Over Pecan Hazard

Silvestri Sweets Inc recalled 37,314 bags of Cookie Butter Holiday Bark on November 21, 2025. The recall stems from undeclared pecan allergens, posing a risk to consumers with nut allergies. The affected product was distributed nationwide through Aldi stores.

Silvestri Sweets Inc dba Carousel Candies
Undeclared pecan
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Food & Beverages
HIGH
FDA FOOD

Silvestri Sweets Recalls Choceur Holiday Bark Over Undeclared Wheat

Silvestri Sweets Inc recalled 37,314 bags of Choceur Pecan Cranberry & Cinnamon Holiday Bark on November 21, 2025. The recall stems from undeclared wheat, a serious allergen risk for consumers. The product was distributed nationwide through Aldi grocery stores.

Silvestri Sweets Inc dba Carousel Candies
Undeclared wheat
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Food & Beverages
HIGH
FDA FOOD

Lotus Mom Corporation Recalls Brass Pot Over Lead Contamination

Lotus Mom Corporation recalled 9 units of its Brass Pital Pot on November 21, 2025, due to potential lead contamination. Consumers should not consume the product and seek refunds or replacements. The affected pot features the sticker label 'BRASS HAMMERED HANDI NO 3' with UPC 7 023672 414398.

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

IKM Aluminum Saucepan Recalled Over Lead Contamination Risk

Lotus Mom Corporation recalled 56 units of its 9-inch aluminum saucepan on November 21, 2025. The product may contain leachable lead, posing serious health risks. Consumers should not use the saucepan and seek refunds immediately.

Lotus Mom Corporation dba Indian Kitchen Mart
Potential contamination
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