All Product Recalls

Browse through 652 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Occluders Over High Hazard

Maquet Cardiovascular recalled the Heartstring III Proximal Seal System on August 15, 2025, due to three identified failure modes. These failures include issues with the seal's loading, deployment, and hemostasis. The recall affects 168 units distributed worldwide.

Maquet Cardiovascular
Three failure
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HIGHFDA FOOD

Anderson Candy Company Recalls Peanut Rounds Over Soy Allergen Risk

Anderson Candy Company recalled 960,000 units of Peanut Rounds on August 15, 2025. The recall stems from undeclared soy allergens that pose a serious health risk. The affected products were distributed in several states including Texas and Louisiana.

Anderson Candy Company
Undeclared soy
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HIGHFDA DEVICE

Exactech Recalls Reverse Shoulder Humeral Liners Over Hazard

Exactech recalled 11,542 reverse shoulder humeral liners on August 15, 2025. The devices have an articular surface position outside of the specified dimensions. This recall affects units distributed worldwide, including several U.S. states.

Exactech
Reverse Shoulder
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HIGHFDA DEVICE

Mindray Recalls BeneVision N1 Patient Monitor Over Alarm Issues

Mindray DS USA, Inc. recalled 2,278 BeneVision N1 Patient Monitors on August 15, 2025. The monitors may activate an abnormal alarm pause, compromising patient safety. Health professionals must cease using these devices immediately and follow recall instructions.

Mindray DS USA, Inc.
Potential for
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Recalled ESR HaloLock Kickstand Wireless Power Bank Model 2G520
HIGH
CPSC

ESR HaloLock Wireless Power Banks Recalled Over Fire Hazard

ESR recalled HaloLock wireless power banks on August 14, 2025, following reports of fire hazards. The lithium-ion batteries can overheat and ignite. Consumers should stop using these devices immediately and return them for a full refund.

ESR HaloLock Wireless Power Banks
The lithium-ion
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HIGHFDA 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 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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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 Werner 20’ and 24’ Multi-Max Pro Multi-Purpose Ladder with location of product label and attached black rope
MEDIUM
CPSC

Werner Recalls Multi-Max Pro Ladders Over Fall Hazard

Werner recalled 20,000 Multi-Max Pro ladders on August 14, 2025 after reports of locking mechanism failures. The recall affects models ALMP-20IAA and ALMP-24IAA sold in silver with blue features. Consumers must stop using the ladders and contact Werner for a refund.

Werner
The ladders'
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HIGHFDA 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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HIGHFDA 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
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HIGHFDA 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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