stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

Food & Beverages
HIGH
FDA FOOD

Tampa Maid Foods Recalls Shrimp Due to Cesium-137 Contamination

Tampa Maid Foods recalled 776 cases of Panko Style Breaded Butterfly Shrimp on August 16, 2025. The product may be contaminated with Cesium-137, a radioactive substance. Consumers should not eat the shrimp and should seek refunds or replacements.

TAMPA MAID FOODS
Product may
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Food & Beverages
HIGH
FDA FOOD

TAMPA MAID FOODS Recalls Shrimp Due to Cesium-137 Contamination

TAMPA MAID FOODS recalled 31 cases of Breaded Butterfly Shrimp on August 16, 2025, due to potential contamination with Cesium-137. The product, sold in bulk packaging, may pose serious health risks. Consumers should not consume the shrimp and seek refunds immediately.

TAMPA MAID FOODS
Product may
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Occluder Due to Failure Risks

Maquet Cardiovascular recalled 32,867 units of the Heartstring III Proximal Seal System on August 15, 2025. Three failure modes can lead to inadequate hemostasis during procedures. Patients and healthcare providers must stop using this device immediately.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Occluder Due to High Risk

Maquet Cardiovascular recalled 16,512 Heartstring III Proximal Seal Systems due to critical failure modes. The recall affects devices distributed globally since August 15, 2025. Users must stop using the device immediately and follow manufacturer instructions.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA 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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Health & Personal Care
HIGH
FDA 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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Health & Personal Care
HIGH
FDA DEVICE

ETHICON Recalls Tissue Control Device for Barb Non-Engagement Risk

ETHICON recalled 516 units of the STRATAFIX Spiral PDS Plus device on August 15, 2025. The recall follows reports of potential barb non-engagement that could affect surgical procedures. Healthcare providers and patients must stop using the device immediately.

ETHICON
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Recalls Reverse Shoulder Humeral Liners Over Safety Concerns

Exactech recalled 61,334 units of Reverse Shoulder Humeral Liners on August 15, 2025. The liners do not meet specified dimensional standards, posing a risk to patients. Healthcare providers and patients must stop using the devices immediately.

Exactech
Reverse Shoulder
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Food & Beverages
HIGH
FDA FOOD

Great Value, Sea Best Frozen Shrimp Recalled Over Cesium-137 Risk

Beaver Street Fisheries recalled 33,164 pounds of Great Value and Sea Best raw frozen shrimp on August 15, 2025. The product may contain Cesium-137, a radioactive substance. Consumers should not consume the affected shrimp and should seek refunds.

Beaver Street Fisheries
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 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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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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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
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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

Philips CT Systems Recalled Due to Hazardous Couch Descent

Philips recalled 73 CT systems on August 13, 2025, due to a risk of the patient support table descending unexpectedly. The recall affects models 728240, 728246, and 728256 distributed worldwide. This recall includes systems sold across the US and several countries globally.

Philips North America
The patient
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