immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Recalls Heartstring III Proximal Seal System 3.8 mm Occluder (32,867 Units) 0

Maquet Cardiovascular recalls the Heartstring III Proximal Seal System, a 3.8 mm intravascular anastomosis occluder used by hospitals worldwide. Three failure modes have been identified: loading failure, deployment failure, and failure to provide adequate hemostasis. Healthcare facilities should stop using the device immediately and follow manufacturer recall instructions.

Maquet Cardiovascular
Three failure
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Food & Beverages
HIGH
FDA FOOD

Anderson Candy Company Recalls 960,000 Peanut Rounds for Undeclared Soy Allergen (2025)

Anderson Candy Company recalled 960,000 Peanut rounds after undeclared soy allergen was found. The sizes are 2.25 oz and 3 oz. The affected distribution covers Oklahoma, Louisiana, Texas, Arkansas, Kansas, Missouri, Arizona, Alabama, Mississippi and Tennessee. Consumers should not eat the product and should contact the company for refund or replacement.

Anderson Candy Company
Undeclared soy
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Health & Personal Care
HIGH
FDA DEVICE

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.

Maquet Cardiovascular
Three failure
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe 61,334 Reverse Shoulder Humeral Liners Recalled Worldwide (2025)

Exactech recalled 61,334 Equinoxe reverse shoulder humeral liners sold worldwide after finding the articular surface position outside labeling dimensions. The recall covers REF 320-38-00, REF 320-38-03, REF 320-42-00, and REF 320-42-03. Healthcare providers and patients should stop using the devices immediately and follow recall instructions distributed by email.

Exactech
Reverse Shoulder
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Food & Beverages
HIGH
FDA FOOD

Great Value and Sea Best Raw Frozen Shrimp Recalled for Cs-137 Contamination (33,164 Lbs) 2025

Beaver Street Fisheries is recalling 33,164 pounds of Great Value and Sea Best raw frozen shrimp distributed to Arkansas, Florida and Illinois after Cs-137 contamination was detected. The product may be contaminated with Cesium-137, a radiological hazard. Consumers should not consume it and should contact Beaver Street Fisheries for refund or replacement.

Great Value
Product may
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Health & Personal Care
HIGH
FDA DEVICE

Ethicon Stratafix PDS Plus Recall 516 Units for Barb Non-Engagement (2025)

Ethicon recalled 516 STRATAFIX Spiral PDS Plus Bidirectional Knotless Tissue Control Devices sold worldwide through healthcare providers, including 18 U.S. states and Singapore and Malaysia. The defect is potential barb non-engagement that could compromise tissue control. Clinicians and patients should stop using the device immediately and follow recall instructions from Ethicon.

Ethicon
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Recalled 11,542 HumeraL Liners Worldwide Over Dimension Mismatch (2025)

Exactech recalled 11,542 Equinoxe reverse shoulder humeral liners worldwide after finding the articular surface position outside labeling specifications. The recall covers several REF numbers and UDIs and is active as of 2025. Healthcare providers were advised to stop using affected liners and follow manufacturer instructions.

Exactech
Reverse Shoulder
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Recalled LED module
HIGH
CPSC

Viewrail Recalls LED Control Module for Floating Stairs Over Fire Hazard

Viewrail recalls the electronic LED module E2-WR used with floating stairs and rails after a fire hazard was identified. The recall covers modules located inside the metal stringer tube at the back of the stairs. The recall was announced by the CPSC on 2025-08-14. Consumers should stop using the module and contact Viewrail for a replacement or refund.

Viewrail
The LED
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Food & Beverages
HIGH
FDA FOOD

AquaStar Frozen Breaded Shrimp Recalled for Cs-137 Contamination (2025)

AquaStar recalled 126 cases of Frozen AquaStar Breaded Shrimp sold at Walmart stores nationwide and Kroger banners after Cesium-137 contamination was detected. The product is contaminated with Cs-137. Consumers who purchased the affected shrimp should not eat it and should contact AquaStar via email for refund or replacement.

AquaStar
Product may
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Food & Beverages
HIGH
FDA FOOD

Kroger Mercado Shrimp and AquaStar Frozen Shrimp Recalled for Cs-137 Contamination (2025)

18,000 bags recalled. AquaStar Cocktail Shrimp and Kroger Mercado Shrimp were pulled after Cs-137 contamination was detected. The recalls cover products sold at Walmart and Kroger stores in multiple states between late July and mid August 2025. Consumers should stop using these products immediately and contact AquaStar for refunds or replacements.

Kroger
Product may
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Recalled Drinkmate 1L Carbonation Bottles
MEDIUM
CPSC

Drinkmate Recalls 1-Liter Carbonation Bottles for Explosion Risk

Drinkmate recalled certain 1-liter carbonation bottles after receiving reports of potential explosions. Users may suffer serious laceration and hearing damage from exploding bottles. Consumers should stop using the bottles immediately and contact Drinkmate for a free replacement.

Drinkmate
The recalled
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Recalled STWUQIKONG Spiral Tower Toy
HIGH
CPSC

STWUQIKONG Three-Tier Spiral Tower Toy Recalled for Choking Hazard (2025)

STWUQIKONG recalled a three-tier spiral tower toy sold on Shein because of a choking hazard. The recall was announced on August 14, 2025. The toy includes three yellow balls and is designed for children under three, violating the small-ball ban. Stop using the product immediately and email STWUQIKONG_RECALL@hotmail.com to receive a full refund.

STWUQIKONG
The recalled
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Recalled Firefly Safe & Green 32 oz. fuel bottles
HIGH
CPSC

Firefly Safe & Green 32 oz. Fuel Bottles Recalled for Poisoning Risk to Children

Firefly Fuel Inc. recalled Firefly Safe & Green 32 oz. bottles. The recall date is August 14, 2025. The fuel is sold in a clear bottle with a white cap and nozzle applicator. The product label shows Firefly brand, Safe & Green in green font, and claims Non-Toxic and Kosher. The nozzle applicator lacks child-resistant features, violating the Poison Prevention Packaging Act and the Federal Hazardous

Firefly Fuel
The recalled
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Tuscan Artichoke and Mozzarella Salad Recalled for Undeclared Allergens (8.5 oz)

Fresh & Ready Foods recalled 233 units of Tuscan Artichoke and Mozzarella Salad distributed to 15 California locations after undeclared wheat and milk allergens were found. The allergen was not declared on the label. Consumers should not eat the product and should contact Fresh & Ready Foods LLC for refunds or replacements via email.

Fresh & Ready Foods
undeclared allergen
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Tag Statistics

Total Recalls
2,756

Related Tags

stop use immediatelyreturn for refundreplacement availableglassmetalelectronicbattery poweredcpsc regulatedfda regulatednhtsa regulatedinfant productadult product