immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Recalls Knee Fusion Nail Due to Assembly Error

Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.

Waldemar Link GmbH & Co. KG
The device
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Over Cracking Hazard

Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.

Draeger
Multiple complaints
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Health & Personal Care
HIGH
FDA DEVICE

Draeger Recalls Airway Connector Due to Cracks in Hose

Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.

Draeger
Multiple complaints
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Diluent Due to Elevated Platelet Counts

Beckman Coulter recalled 76,098 units of COULTER DxH Diluent on November 10, 2025. The recall affects specific lots contributing to elevated platelet background counts in analyzers. Healthcare providers and patients must stop using this product immediately.

Beckman Coulter
Due to
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Food & Beverages
HIGH
FDA FOOD

Kosher First Recalls Herring Due to Undeclared FD&C Red #40

Kosher First recalled 283 units of Shloimy's Heimishe Matjes Herring on November 10, 2025, due to undeclared FD&C Red #40. The recall affects products distributed in New York and poses a high risk of allergic reactions. Consumers should not consume the product and seek refunds or replacements.

Kosher First
Undeclared FD&C
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Vehicles & Parts
HIGH
NHTSA

Toyota recall affects 2023-2025 models, instrument cluster display may fail

Toyota Motor Engineering & Manufacturing recalls multiple 2023-2025 vehicles because the instrument panel may fail to display speed, braking and tire pressure alerts. Dealers will update software for non-PHEV models and inspect/possibly replace panels for PHEV models at no charge. Owner letters expected Oct 27, 2025. Contact Toyota at 1-800-331-4331; Lexus follow numbers 25LB05/25LA05.

Toyota
An instrument
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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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Vehicles & Parts
HIGH
NHTSA

Ford recalls 2025 Explorer and other models for possible fuel injector leak linked to fire risk (24S

Ford Motor Company recalled 2023 Lincoln Corsair, 2023-2024 Escape, 2024 Mustang, and 2025 Explorer vehicles due to fuel injector assembly lacking O-ring support discs. The defect may cause a fuel leak with ignition risk. Dealers will install new fuel injector O-rings and O-ring support discs at no charge. Owner letters mailed Oct 7, 2024. Ford contact: 1-866-436-7332. Recall number 24S54.

Ford Motor Company
A fuel
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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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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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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

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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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

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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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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