2,143 recalls tagged with “cpsc regulated”.
Honda is recalling 2021-2025 Acura TLX, 2023-2025 Acura MDX, and 2023-2025 Honda Pilot vehicles over a brake pedal pivot pin that may loosen. The defect can shift the pedal, reducing braking ability. Dealer repairs are free. Honda notified owners on July 29, 2025. Contact Honda at 1-888-234-2138.
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.
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.
Meridian Bioscience recalled 211 units of the Revogene C. difficile diagnostic assay on December 5, 2025. Users may experience false-negative results due to a decline in performance over time. Patients and healthcare providers must stop using the device immediately.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.