All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Food & Beverages
HIGH
FDA FOOD

Chefs Warehouse Recalls 15 Lbs of Cucumber Slices for Salmonella Contamination (2025)

Chefs Warehouse recalls 15 pounds of cucumber slices after Salmonella contamination was detected. The recall covers 10-pound and 5-pound packages labeled 5# Lot#B0515465 and 5# Lot#B0515867 distributed to Maryland, Delaware and Virginia. Consumers should not consume the recalled cucumbers and should contact Chefs Warehouse for refund or replacement.

Chefs Warehouse
Product is
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Food & Beverages
HIGH
FDA FOOD

Chefs Warehouse Recalls 5 lb Diced Cucumber for Salmonella Contamination (2025)

Chefs Warehouse recalled 5 lb diced cucumber distributed to Maryland, Delaware and Virginia after FDA confirmation of Salmonella contamination. The product is a 5 lb bag labeled 5# Lot#B0515911. Consumers should not consume the recalled cucumber and should contact Chefs Warehouse for refund or replacement.

Chefs Warehouse
Product is
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Food & Beverages
HIGH
FDA FOOD

Chefs Warehouse Cucumber Recall 98-Case Batch Salmonella Contamination (2025)

Chefs Warehouse recalled 98 cases of cucumber distributed to Maryland, Delaware and Virginia after Salmonella contamination was detected. The product is contaminated with Salmonella. Consumers who bought this cucumber should not consume it and should contact Chefs Warehouse for a refund or replacement.

Chefs Warehouse
Product is
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Recalls 1,440 Simplera Sensor Units Over Label Adhesion Risk (2025)

Medtronic MiniMed recalled 1,440 Simplera Sensor units distributed outside the United States after a device cap label may not adhere, risking sterility. The defect could increase infection risk. Patients and healthcare providers should stop using the device and follow recall instructions provided by Medtronic MiniMed or their healthcare provider.

Medtronic MiniMed
The device
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Food & Beverages
HIGH
FDA FOOD

Ventura Foods Recalls Peanut Butter and Jelly Due to Plastic Hazard

Ventura Foods recalled 929 cases of peanut butter and grape jelly on April 30, 2025. The company found pieces of blue plastic in the product during production. Consumers should not consume this product and can seek refunds or replacements.

Ventura Foods
Foreign material.
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Food & Beverages
HIGH
FDA FOOD

Turkana Food Floria Dried Apricots Recalled in 352-Case High-Hazard Alert (2025)

Turkana Food Inc. recalled 352 cases of Floria Dried Apricots, 200-gram packages, distributed to retailers in 19 states. The recall was issued on April 29, 2025. The product contains undeclared sulfites. Consumers should not eat it and should contact Turkana Food Inc. for refund or replacement via email.

Turkana Food
Product contains
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Health & Personal Care
HIGH
FDA DEVICE

3M Ranger Blood/Fluid Warming High Flow Set Recall Affects 530,470 Units

3M recalled 530,470 Ranger Blood/Fluid Warming High Flow Sets due to incorrect flow rates and outlet temperature locations. This defect can affect the warming of fluids, posing serious risks to patients. Healthcare providers must stop using these devices immediately and follow the manufacturer’s instructions for returns.

3M
Field action
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Vehicles & Parts
HIGH
NHTSA

Honda ADV160 Recall 2025 for Oil Pump Gear Loss of Drive Power

Honda recalled 2024-2025 ADV160 scooters after discovering the oil pump driven gear may fail, causing a loss of drive power. The loss of drive power could lead to a crash. Owner letters were mailed August 6, 2025, and dealers will replace the gear free of charge under recall KR9.

Honda
Loss of
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Health & Personal Care
HIGH
FDA DEVICE

ESAOTE Endocavity Ultrasonic Probe E 3-12 Recall Affects 5 Units (2025)

ESAOTE recalled 5 Endocavity Ultrasonic Probe E 3-12 units sold in the United States to healthcare providers in NC and TX. A potential weakness in the probe body could cause liquid to leak from the terminal part of the casing near the cable. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions.

ESAOTE
A potential
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Vehicles & Parts
HIGH
NHTSA

Kia EV9 Recalled for Rear GDU Weld Flaw in 2025 Model Year

Kia America, Inc. recalls 2025 EV9 vehicles for a damaged rear gear drive unit shaft from improper welds. The defect can cause loss of drive power and raise crash risk. Kia asks owners to contact dealers for a free replacement and lists SC337 as the recall number.

Kia America, Inc.
A loss
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Vehicles & Parts
HIGH
NHTSA

BMW 2025 X3 Recalled for Electrical Cable Overheating After Tightening Issue

BMW recalls 2025 X3 30 xDrive vehicles due to an overheated positive battery cable connection that can cause engine stall and fire risk. The recall affects 2025 X3 models and affects owners nationwide. Dealers will inspect and tighten or replace the positive battery cable and starter-generator at no charge. Letters to owners were mailed June 5, 2025.

BMW
An overheated
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Health & Personal Care
HIGH
FDA DRUG

World Perfumes Inc. Recalled Iodo Blanco Iodides First Aid Antiseptic Over Leaking Containers (2025)

World Perfumes Inc. recalled 3,900 bottles of Iodo Blanco Iodides First Aid Antiseptic in Florida after broken or leaking containers were reported. The recall covers iodine 2% antiseptic distributed by Essential Products. Consumers should stop use immediately and contact World Perfumes or a healthcare provider for guidance.

World Perfumes
Defective Container:
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Health & Personal Care
HIGH
FDA DEVICE

MEDITECH Expanse Lab Calculator Module Recalled for Input Error Risk in 2025

MEDITECH released an active recall for the Expanse Laboratory calculator/data processing module. The recall covers 148 units distributed worldwide, including the US, UK, Canada, Ireland and the British Virgin Islands. The hazard concerns simultaneous multi-key inputs potentially removing data from the first field in screens or questionnaires.

Medical Information Technology
Entering multiple
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