immediate action Recalls

2,756 recalls tagged with “immediate action”.

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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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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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Recalls Vascular Tray Over Detaching Handle Hazard

Merit Medical Systems recalled 864 units of its Custom Waste Management Kit Vascular Tray on December 4, 2025. The handle of the inflation device may detach from the syringe during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.

Merit Medical Systems
Inflation device
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Recalls Custom Manifold Kit Due to Detachment Risk

Merit Medical Systems recalled 2,192 units of its Custom Manifold Kit on December 4, 2025. The inflation device handle may detach from the syringe during procedures. This poses a significant risk to patients and healthcare providers.

Merit Medical Systems
Inflation device
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Health & Personal Care
HIGH
FDA DEVICE

Mobius Imaging Recalls AIRO CT X-ray Pendant Over Safety Label Issue

Mobius Imaging recalled 101 units of the AIRO Computed Tomography X-ray system pendant on December 4, 2025. The pendants lack a critical "Safe Hand Position Warning" label, posing a safety risk for healthcare providers. Users should immediately stop using these devices and follow recall instructions.

Mobius Imaging
AIRO pendant
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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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FUFU&GAGA White Wood Frame Queen Size Murphy Wall Bed (unfolded)
MEDIUM
CPSC

FUFU&GAGA Murphy Wall Beds Recalled for 215-Pound Fall Hazard (2025)

Ningbo Tianqi Electronic recalled FUFU&GAGA white wood frame queen-size Murphy wall beds sold at Home Depot and Lowes. The model KF210284US-01MH-A001 may fall during assembly or disassembly. Consumers should stop using the recalled wall beds and contact Ningbo Tianqi Electronic for a full refund.

FUFU&GAGA
During assembly
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Recalled Primark Water Balloon Pump (front)
MEDIUM
CPSC

Primark Water Balloon Pumps Recall 5252801 Over Rupture Hazard (2025)

Primark US recalls Primark Water Balloon Pumps due to rupture risk. The affected units were sold at Primark stores in the United States from March 2023 through July 2023 for about $6. Consumers should stop using the pumps immediately and return them to a Primark store for a full refund.

Primark
The water
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Recalls Impella 5.5 Devices Due to Packaging Error

Abiomed recalled two units of the Impella 5.5 with SmartAssist on December 4, 2025. The devices were packaged in incorrect outer cartons, posing a potential hazard. Patients and healthcare providers must stop using the devices immediately.

Abiomed
Device packaged
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Recalled KTEBO Writing Tablet Toys in Blue/Pink (front)
HIGH
CPSC

KTEBO Writing Tablet Toys Recalled Over Battery Ingestion Risk on Amazon (2025)

KTEBO recalled its Writing Tablet Toys sold on Amazon on December 4, 2025. The screw securing the battery compartment containing a button cell battery does not remain attached as required. This creates a risk of ingestion with potential serious injury or death. Consumers should stop using the 2-pack sets immediately and contact KTEBO for a free replacement.

KTEBO
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Recalls Inflation Kits Due to Handle Detachment Hazard

Merit Medical Systems recalled 18,897 custom inflation kits on December 4, 2025. The inflation device handle may detach from the syringe during use, posing a risk of injury. Healthcare providers and patients should stop using the device immediately.

Merit Medical Systems
Inflation device
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Recalls Inflation Device Due to Detachment Hazard

Merit Medical Systems recalled 173,645 Allwell Inflation Devices on December 4, 2025. The device handle may detach from the syringe during procedures, posing a high hazard. Healthcare providers and patients should stop using the device immediately.

Merit Medical Systems
Inflation device
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Recalled 14 oz. Sport Tumbler in Cowgirl, Sports, Daisy Checkers, Dinosaur and Bows patterns
HIGH
CPSC

HydroJug Recalls 14-Ounce Children’s Sport Tumblers for Choking Hazard (2025)

HydroJug recalls its 14-ounce children’s sport tumbler sold through HydroJug's online store after reports of a choking hazard. The rivet-attached handle can loosen and detach from the lid, posing a choking risk to children. Stop using the tumbler and contact HydroJug at service@thehydrojug.com for a free replacement lid.

HydroJug
The rivets
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Systems Recalls Angioplasty Packs Over Detachment Hazard

Merit Medical Systems recalled 328,000 angioplasty packs on December 4, 2025, due to a risk of the inflation device handle detaching during procedures. The recall affects devices distributed worldwide, including states across the U.S. Healthcare providers and patients must stop using the devices immediately.

Merit Medical Systems
Inflation device
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Food & Beverages
HIGH
FDA FOOD

Lil' Turtles Recalls Tomato Basil Soup for Undeclared Milk Allergen

Lil' Turtles recalled 110 cases of Grandma Belle's Tomato Basil Soup on December 4, 2025. The product contains undeclared milk, posing a risk to consumers with milk allergies. Consumers should stop using the soup and contact the manufacturer for a refund.

Lil Turtles
Undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

Mobius Imaging Recalls AIRO CT X-ray Pendant Due to Safety Risk

Mobius Imaging recalled 26 units of the Detachable 10in Pendant Upgrade for the AIRO CT X-ray System on December 4, 2025. The devices lack a critical "Safe Hand Position Warning" label, posing a high risk during operation. Healthcare providers and patients must cease use immediately and follow the manufacturer's instructions.

Mobius Imaging
AIRO pendant
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical Recalls Custom Procedure Kits Due to Detachment Hazard

Merit Medical Systems recalled multiple Custom Procedure Kits on December 4, 2025, due to a risk of the inflation device handle detaching from the syringe during use. The recall affects several reference numbers sold worldwide, including in the U.S. and various international markets.

Merit Medical Systems
Inflation device
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