2,153 recalls tagged with “stop use immediately”.
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.
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.
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.
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.
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.
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 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.
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 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.
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.
Cubimana recalled treehouse building toy sets sold on Shein by Vatos Toys from July 2025 through October 2025. The recall list includes 618-piece sets and a LED light component containing a button cell battery. Parents should stop using the toy immediately and contact Vatos Toys for a full refund.
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.
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.
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.
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.
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 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.
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.
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.
Philips North America recalled one unit of its MR system on December 3, 2025, due to potential stiffness value errors in MR Elastography maps. The recall affects systems with software versions R11.1 and R12.1, distributed worldwide. Healthcare providers should stop using the device immediately and follow the manufacturer's instructions.