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

AquaStar Cocktail Shrimp Recalled Due to Cesium-137 Contamination

AquaStar recalled 22,500 cases of its Cocktail Shrimp on August 14, 2025, due to potential contamination with Cesium-137. The shrimp was sold at Walmart stores across 25 states between July 31 and August 16, 2025. Consumers should not consume the product and seek a refund.

AquaStar
Product may
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Recalled LED module
HIGH
CPSC

Viewrail Recalls LED Modules Due to Fire Hazard Risk

Viewrail recalled electronic LED modules on August 14, 2025, due to a fire hazard. The model "E2-WR" can overheat and melt, posing risks to consumers. Affected modules were sold from August 2023 through June 2025 for about $80.

Viewrail
The LED
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Recalled STWUQIKONG Spiral Tower Toy
HIGH
CPSC

STWUQIKONG Recalls Children's Toys Over Choking Hazard

STWUQIKONG recalled children's tower toys on August 14, 2025, due to a choking hazard. The toys contain small balls and violate the small ball ban, posing risks to children under three years. Consumers must stop using the toys immediately and return them for a full refund.

STWUQIKONG
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT Systems Recalled Due to Patient Support Table Hazard

Philips recalled 181 CT scanner units on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728235, 728231, and 728317 distributed worldwide. Healthcare providers and patients must stop using these devices immediately to ensure safety.

Philips North America
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Hematology Analyzers Due to High HGB Risk

Beckman Coulter recalled its UniCel DxH 800 COULTER Cellular Analysis System on August 13, 2025. This recall affects devices that may produce inaccurately high hemoglobin results in patients with high white blood cell counts. The recall impacts worldwide distribution including numerous states in the U.S. and many countries.

Beckman Coulter
Hematology analyzers
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Sandwiches Over Undeclared Allergens

Fresh & Ready Foods LLC recalled 233 units of Piccolo Pranzo Box sandwiches on August 13, 2025. The recall follows the discovery of undeclared allergens, specifically wheat and milk, posing a serious risk to consumers. The recalled products were distributed to 15 locations across California.

Fresh & Ready Foods
undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT System Recalled Due to Unexpected Descent Hazard

Philips recalled 6 CT 6000 systems on August 13, 2025. The patient support table may descend unexpectedly due to a ball screw misalignment. This recall affects devices distributed worldwide, including the U.S.

Philips North America
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Hematology Analyzer Recalled for High HGB Risk

Beckman Coulter recalled the UniCel DxH 900 COULTER Cellular Analysis System on August 13, 2025, due to erroneous high hemoglobin results. The devices may misreport hemoglobin levels on samples with elevated white blood cell counts. This recall affects devices distributed worldwide, including the U.S.

Beckman Coulter
Hematology analyzers
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Hematology Analyzers Over High HGB Results

Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System on August 13, 2025. Erroneously high hemoglobin results may occur in patients with elevated white blood cell counts. Healthcare providers and patients must stop using the device immediately.

Beckman Coulter
Hematology analyzers
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls CT Systems Over Hazardous Couch Descent

Philips recalled 33 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. A misalignment in the ball screw can cause the couch to drop to its lowest position. The recall affects models distributed worldwide, including the U.S. and numerous countries.

Philips North America
The patient
Read more
Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Hematology Analyzers Over High HGB Risk

Beckman Coulter recalled the UniCel DxH 600 Cellular Analysis System on August 13, 2025. The devices may produce erroneously high hemoglobin results in patients with elevated white blood cell counts. This recall affects medical facilities worldwide, including the United States.

Beckman Coulter
Hematology analyzers
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls CT Systems Over Risk of Unexpected Descent

Philips recalled three Ingenuity CT Family systems on August 13, 2025, due to a hazard that could lead to sudden descent. The issue stems from a ball screw misalignment affecting the patient support table. Users should stop using the devices immediately and follow recall instructions.

Philips North America
The patient
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls CT Systems Over Risk of Unexpected Descent

Philips recalled 285 CT systems on August 13, 2025, due to a risk of patient support tables descending unexpectedly. The recall affects model numbers 728321, 728323, and 728326. Users should stop using the devices immediately and follow manufacturer instructions.

Philips North America
The patient
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Recalls CT Systems Over Risk of Unexpected Descent

Philips recalled 24 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The issue stems from a misalignment in a component after replacement. Health providers must stop using these devices immediately.

Philips North America
The patient
Read more
Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Ciabatta Sandwiches Over Allergen Risk

Fresh & Ready Foods LLC recalled 233 units of Spanish Club Ciabatta sandwiches on August 13, 2025. The recall stems from undeclared allergens, specifically wheat and milk, posing a high risk to consumers. The products were available at 15 corporate locations across California.

Fresh & Ready Foods
undeclared allergen
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Sandwiches Over Wheat Allergen Risk

Fresh & Ready Foods recalled 233 units of ready to eat sandwiches on August 13, 2025. The recall stems from undeclared wheat allergens that pose a serious risk to consumers. The sandwiches were distributed to 15 corporate locations in California.

Fresh & Ready Foods
undeclared allergen
Read more
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