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

3,615 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

Pacific Seafood Recalls 15,498 Lbs Raw Blackened Shrimp Peeled & Deveined Tail-Off Over Sulfite (202

Pacific Seafood recalled 15,498 pounds of Raw Blackened Shrimp Peeled & Deveined Tail-Off sold refrigerated after undeclared sulfite was detected. The product is a shrimp tray produced in Ecuador and distributed in Alabama, Florida and Massachusetts. Consumers should not eat the product and should contact Pacific Seafood Group for a refund or replacement.

Pacific Seafood
Undeclared Sulfite.
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Food & Beverages
HIGH
FDA FOOD

ByHeart Infant Formula Recalled Due to Botulism Risk

ByHeart announced a recall of over 6.9 million units of its infant formula on November 8, 2025, due to contamination with Clostridium botulinum. The recall affects both cans and single-serve packets sold nationwide. Parents are urged to stop using the affected products immediately to prevent serious health risks.

ByHeart
Contaminated with
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Vehicles & Parts
HIGH
NHTSA

Gulf States Toyota Recalls 2025 Camry Hybrid Over Load Capacity Label Inaccuracies

Gulf States Toyota, Inc. recalls 2025 Camry Hybrid vehicles equipped with GST accessories after discovering load carrying capacity labels may display inaccurate added weight values. The mislabeling could cause the vehicle to be overloaded, increasing the risk of a crash. Owners should contact GST for a free label replacement; letters were mailed September 16, 2024.

Gulf States Toyota
A vehicle
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Food & Beverages
HIGH
FDA FOOD

Costco Recalls 142,532 Kirkland Signature Caesar Salad Units Over Plastic Dressing Packet (2025)

Costco Wholesale Corp is recalling 142,532 Kirkland Signature Caesar Salad units sold nationwide after discovering the 3oz sealed Caesar Dressing packet may contain plastic material. The dressing packet inside the salad may contain plastic material. Consumers who bought this product should not eat it and should contact Costco for a refund or replacement.

Costco
The 3oz.
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Health & Personal Care
HIGH
FDA DRUG

Actavis Recalls Testosterone Gel Due to Leakage Risk

Actavis Laboratories recalled 15,944 cartons of Testosterone Gel on November 7, 2025. The recall follows a defect in the side-seal of the containers, which may allow product leakage. Consumers must stop using the product immediately and contact their healthcare providers for guidance.

TESTOSTERONE
Defective Container
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Food & Beverages
HIGH
FDA FOOD

Anthony's BBQ Sauce Recalled for Undeclared Fish Allergen

Anthony's Barbecue & Dip-It Sauce is recalled due to an undeclared fish allergen. The recall affects 192 glass bottles with UPC 6 89076 62272 1. Consumers should not consume the sauce and contact the company for a refund.

Anthony's BBQ
Undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

Da Vinci Surgical Systems Recalled Due to Diagnostic Software Flaw

Intuitive Surgical recalled 219 da Vinci surgical systems on November 7, 2025, due to a software error. This error allowed malfunctioning instrument arms to remain in clinical use, posing a high risk of failure. Healthcare providers and patients must stop using these systems immediately.

Intuitive Surgical
Due to
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Front view of Recalled Napei Collapsible Infant Bath Tub
HIGH
CPSC

Napei Infant Bath Tubs Recalled for Button Battery Ingestion Hazard (2025)

Napei recalled its collapsible infant bath tubs sold on Amazon by Sefon Store after discovering the built-in thermometer uses button cell batteries that are accessible to children. The batteries pose a risk of ingestion, which can cause serious injuries or death. Stop using the tub immediately and contact Sefon Store for a free replacement battery compartment.

Napei
The recalled
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Recalled Vevor Baby Swing in White/Gray with White Base and Mosquito Net, Model Number BB501
HIGH
CPSC

Sanven Technology Recalls 3 Vevor Baby Swing Models for Suffocation Risk (2025)

Sanven Technology recalls 3 Vevor Baby Swing models on 2025-11-06 for a suffocation risk linked to an incline greater than 10 degrees. The swings carry the VEVOR trademark and are labeled as Multi-Function Electric Swing with model numbers BB501K, BB702A, and BB005. Consumers should stop using the swings immediately and contact Sanven Technology for a full refund.

Sanven Technology
The swings
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Recalled Umeyda Shortsleeve Nightgown – Baby Pink Stripe
HIGH
CPSC

Umeyda Nightgowns Recalled for Burn Risk in 2025 Sold on Amazon

Umeyda recalled 100% cotton girls' nightgowns sold on Amazon. The recall involves nightgowns with a pocket and a front button closure. The garments do not meet mandatory flammability standards and pose a burn risk. Stop using them and email ameyda123@163.com for a full refund.

Umeyda
The recalled
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Food & Beverages
HIGH
FDA FOOD

Ventura Foods Publix Deli Carolina-Style Mustard BBQ Sauce Recalled for Foreign Objects (700 Cases)

Ventura Foods recalled Publix Deli Carolina-Style Mustard BBQ Sauce on Nov 6, 2025 after foreign objects were found in granulated onion. The lot is B28725, with 700 cases distributed to 7 retailers across 42 locations and one Costa Rica customer. Consumers should not consume the sauce and should contact Ventura Foods for refund or replacement via email.

Ventura Foods
foreign objects
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Recalled Inkari Plush Alpacas - Naturals
HIGH
CPSC

Inkari Plush Alpaca Toys Recalled for Choking Hazard in 2025

Inkari recalled plush alpaca toys sold through multiple retailers after eyes detach, creating a choking hazard for children under three. The eyes can detach, violating the small parts ban. Consumers should stop using the recalled plush toys and contact Inkari for a full refund.

Inkari
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Famotidine Injection Recall Expands for Microbial Contamination in 2.2 Million Vials

Fresenius Kabi USA, LLC recalls 2,199,850 vials of Famotidine Injection, U.S. distribution nationwide plus Alaska, Hawaii and Puerto Rico after endotoxin testing concerns. The microbial contamination risk prompted an immediate stop-use order. Healthcare providers and patients should follow recall guidance and seek alternatives through their providers.

Famotidine
Microbial Contamination
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Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Ureteral Stent Kit Recalled Due to Labeling Discrepancy

C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual stent size to differ from the labeled size. Healthcare providers and patients should stop using the device immediately.

C.R. Bard
Labeling discrepancy;
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