All Product Recalls

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

Health & Personal Care
HIGH
FDA DRUG

ORL Kids Toothpaste Recalled Due to cGMP Deviations

ORL Labs recalled 1,458 containers of ORL Kids Natural Toothpaste, Bubblegum Flavor, on December 8, 2025. The recall follows cGMP deviations that could pose health risks. Consumers should stop using the product immediately.

ORL Labs
cGMP Deviations
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Health & Personal Care
HIGH
FDA DEVICE

IMRIS Imaging Recalls Head Fixation Device Over Safety Concerns

IMRIS Imaging recalled 122 Head Fixation Devices on December 8, 2025. A torque screw may crack or separate, posing serious risks during surgical procedures. Healthcare providers must stop using the device and follow recall instructions immediately.

IMRIS Imaging
Torque screw
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Health & Personal Care
HIGH
FDA DEVICE

Securitas Healthcare Recalls 900 MHz Call Stations Over Firmware Issue

Securitas Healthcare recalled 5,627 Arial 900 MHz Call Stations on December 8, 2025. A firmware issue may prevent low battery alerts from being transmitted, posing a risk. Affected devices were sold worldwide, including the US and Canada.

Securitas Healthcare
Securitas Healthcare
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Food & Beverages
HIGH
FDA FOOD

Goldenroot Ginger Beer Recalled Over Pasteurization Issues

Goldenroot recalled 1,066 cases of Lemon Ginger Elderberry Ginger Beer on December 8, 2025. The product may contain unpasteurized ginger juice, posing a health risk. Consumers should stop using the product immediately and seek a refund or replacement.

Weaver's Brew
Ginger Beer
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Health & Personal Care
HIGH
FDA DEVICE

Securitas Healthcare Recalls 900 MHz Call Station Over Battery Alert Failure

Securitas Healthcare recalled 1,898 units of the Arial 900 MHz Call Station on December 8, 2025. A firmware issue may prevent low battery alerts, posing a risk of battery failure. Users should stop using the device immediately and follow recall instructions.

Securitas Healthcare
Securitas Healthcare
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Food & Beverages
HIGH
FDA FOOD

Keurig Recalls McCafe Decaf Coffee Pods Due to Caffeine Risk

Keurig Green Mountain recalled 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods on December 6, 2025. The product is inaccurately labeled as decaf but may contain caffeine. Consumers in CA, IN, and NV should not consume the pods and seek refunds.

Keurig DR Pepper
Product is
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Health & Personal Care
HIGH
FDA DEVICE

LimFlow Vector Medical Device Recalled Due to Expiration Date Error

LimFlow recalled 33 units of its Vector model VT-US-23 on December 5, 2025, due to incorrect expiration dates. Patients and healthcare providers should stop using this device immediately. The recall affects distribution across 14 states and the District of Columbia.

LimFlow
Incorrect expiration
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Food & Beverages
HIGH
FDA FOOD

Evergreen Refreshments Tacos Recalled Due to Foreign Material

Fresh & Ready Foods recalled 200 units of its Evergreen Refreshments brand Ready to Eat Tacos on December 5, 2025. The product may contain foreign material posing a health risk. Consumers should not eat the product and seek a refund.

Fresh & Ready Foods
Foreign material.
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Health & Personal Care
HIGH
FDA DEVICE

Beaver-Visitec Recalls Laser and Endoscopy System Over Safety Hazard

Beaver-Visitec International recalled five units of the OME6000U Laser and Endoscopy System on December 5, 2025. The recall stems from a manufacturing deviation where ferrites required for the USB cable were not installed. This omission poses a high electrical hazard risk to patients and healthcare providers.

Beaver-Visitec International
Manufacturing deviation
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Food & Beverages
HIGH
FDA FOOD

Bharat Bazar Recalls Asafoetida Due to Undeclared Wheat

Bharat Bazar recalled 180 packages of SOMA Kitchen Natural Asafoetida on December 5, 2025, due to undeclared wheat. The product, sold in 4-ounce containers, poses a high risk of allergic reactions for those with wheat allergies. Consumers should stop using the product immediately and contact Bharat Bazar for refunds.

BHARAT BAZAR
Undeclared wheat.
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Recalls LUMINOS Medical Imaging Systems Over Collimation Risk

Siemens Medical Solutions USA recalled LUMINOS Lotus Max and Luminos dRF Max systems on December 5, 2025. The recall affects systems with software version VF11 and involves a potential collimation error. Healthcare providers and patients must stop using the devices immediately.

Siemens Medical Solutions USA
A potential
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Breakfast Burritos for Foreign Material

Fresh & Ready Foods recalled 93 units of Spicy Breakfast Burrito on December 5, 2025, due to foreign material contamination. The burritos were sold in Oregon and Washington. Consumers should not eat the product and seek refunds or replacements.

Fresh & Ready Foods
Foreign material.
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Recalled INIU Power Bank – model BI-B41
HIGH
CPSC

INIU Recalls 10,000mAh BI-B41 Power Banks Over Fire Hazard (2025 Recall)

INIU recalled 10,000mAh portable power banks sold on Amazon after identifying a fire risk from overheating. The recall covers BI-B41 models with serial numbers 000G21, 000H21, 000I21 and 000L21. Consumers should stop using the recalled power banks immediately and contact INIU for a full refund.

INIU
The lithium-ion
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Tacos Due to Foreign Material Hazard

Fresh & Ready Foods recalled 62 units of Spicy Egg Potatoes Cheese Tacos on December 5, 2025. The product may contain foreign material posing a health risk. Consumers should not eat the tacos and seek refunds immediately.

Fresh & Ready Foods
Foreign material.
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Food & Beverages
HIGH
FDA FOOD

Fresh & Ready Foods Recalls Breakfast Burrito Over Foreign Material

Fresh & Ready Foods recalled 278 units of Spicy Veggie Breakfast Burrito on December 5, 2025. The recall occurred due to foreign material found in the product. Consumers should not eat the burrito and should seek a refund or replacement.

Fresh & Ready Foods
Foreign material.
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Recalled Grizzly Industrial 15” 3HP Heavy-Duty Planer
MEDIUM
CPSC

Grizzly Industrial Recalls G0815 15-Inch Planer for Debris Ejection Hazard

Grizzly Industrial is recalling all G0815 15-inch heavy-duty planers sold nationwide. The recall covers units from June 2016 through September 2025. The chip breaker can contact cutterhead blades and eject debris, posing an injury risk to users and bystanders. Stop using the recalled planers and contact Grizzly for a free repair kit and installation instructions.

Grizzly Industrial
The chip
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