Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
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.
CreateOn recalled Crayola pip-Cubes magnetic building cubes due to a magnet ingestion hazard. The recall is active. Consumers should stop using and contact CreateOn for a replacement.
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.
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.
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.
Little Pea Shop recalled two styles of crib bumpers sold by Little Pea Shop after violating the Safe Sleep for Babies Act. The recalled padding can obstruct an infant’s breathing, creating a suffocation risk. Parents should stop using the recalled bumpers immediately and contact Little Pea Shop for a full refund.
Casaottima recalled its 13-drawer dressers sold on Amazon after a risk of serious injury or death from tip-over and entrapment. The dressers can tip if not anchored to a wall. Stop using the recalled furniture and contact Casaottima for a full refund.
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.
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.
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 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.
Healthy Truth recalled 88 pounds of Moringa Powder on December 4, 2025. The products may be contaminated with Salmonella Richmond. Consumers in MD, NC, WA, CT, and PA should not consume the product.
AZ Gems, Inc. recalled 1,099 cases of Jumbo RAW SHRIMP on December 4, 2025, due to elevated chloramphenicol levels. The shrimp, sold under the Member's Mark label, poses a significant health risk. Consumers should not consume the product and seek refunds or replacements immediately.
Medtronic recalled its Abre Venous Self-Expanding Stent System on December 4, 2025, due to a potential Nitinol anomaly. This issue may lead to reduced stent diameter and corresponding radial force, increasing the risk of stent migration. The recall affects 442 units distributed worldwide, including the U.S.
Merit Medical Systems recalled 4,163,123 inflation devices on December 4, 2025, due to a risk that the handle may detach during use. This defect poses a high hazard to patients and healthcare providers. Consumers should stop using the device immediately and follow the manufacturer’s instructions for returns.
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 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 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.
Intuitive Surgical recalled 110,580 Ion Vision Probe Bags on December 4, 2025, due to compromised sterile seals. The recall affects devices distributed throughout the United States and several countries including Australia and Germany. Patients and healthcare providers should stop using the product immediately.
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.