1,716 recalls tagged with “cpsc regulated”.
Vasicar recalled 18,000 dressers on January 8, 2026, due to tip-over risks. The dressers can cause serious injury or death if not anchored to the wall. Consumers should stop using them immediately and seek a refund.
Joyful Journeys recalled baby loungers on January 8, 2026, due to serious injury risks. The loungers pose fall and entrapment hazards to infants. Consumers should stop using them immediately and seek a refund.
RH recalled its Natural Antler Chandeliers on January 8, 2026, due to an impact hazard. The chandeliers can detach if hung at an angle, posing a risk of falling. Consumers should stop using the product immediately and contact RH for repairs.
Sangohe recalled adult portable bed rails on January 8, 2026, after identifying risks of serious injury and death. The bed rails can entrap users, leading to potential asphyxiation. Consumers should stop using the product immediately and seek a full refund.
Agrish recalled adult portable bed rails on January 8, 2026. The recall affects models 2512, 2513, and 2516 due to an entrapment hazard. Consumers should stop using the product and seek a full refund.
Infant Innovations recalled BabyBond retractable safety gates on January 8, 2026, due to a risk of serious injury or death from entrapment. The gates can allow a child's torso to fit through an opening, violating safety standards. Consumers should stop using the gates immediately and seek a refund.
Marcus Adler Glove recalled Julie and Judah pajama pants and shorts on January 8, 2026. The products violate mandatory flammability standards for children's sleepwear. Consumers should immediately stop using these items and seek a refund.
Lterfear recalled the Multifunction Pounding Game model D888 on January 8, 2026. The toy poses a serious ingestion hazard due to high-powered magnets that can detach. Consumers should stop using the toy immediately and seek a refund.
Rattan recalled its 6-Drawer Dressers on January 8, 2026, due to serious tip-over and entrapment risks. The unstable dressers pose a significant danger to children, especially if not anchored. Consumers should stop using these dressers immediately and seek a full refund.
Medline Industries recalled 150 dialysis convenience kits on January 8, 2026, due to silicone seal defects. Affected kits may obstruct fluid paths and risk exposure to biological contaminants.
Medline Industries recalled 14,525 dialysis convenience kits on January 8, 2026. The recall affects multiple product SKUs due to potential silicone seal failures. These issues may cause therapy delays or exposure to contaminants.
Outside The Breadbox recalled 4,497 units of bread crumbs on January 8, 2026. The product contains undeclared allergens: egg and milk. Consumers in CO, MS, ND, NE, RI, TN, TX, and WI should not consume the product.
Medline Industries recalled 1,212 kits containing Tego Connectors on January 8, 2026. The recall stems from issues with silicone seals that may cause occluded fluid paths. Users may experience delays in therapy or exposure to contaminants due to this defect.
Medline Industries recalled 516 medical kits on January 8, 2026, due to issues with Tego Connectors. The silicone seal may tear or dome, posing a high risk of therapy interruption and exposure to contaminants. Healthcare providers must stop using these devices immediately and follow recall instructions.
Medline Industries recalled 2,020 dialysis kits on January 8, 2026, due to defective silicone seals. The seals may dome or tear, leading to fluid leaks and contamination. Patients and healthcare providers should stop using these kits immediately.
Medline Industries recalled 31,848 dialysis dressing change kits on January 8, 2026. The recall follows reports of defective silicone seals on Tego Connectors that may occlude fluid paths. This defect can delay therapy and expose patients to biological contaminants.
Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.
Medline Industries recalled 9,720 convenience kits on January 7, 2026, due to sterilization calibration issues. The affected products may not meet sterility assurance levels. Patients and healthcare providers should stop using these kits immediately.
Medline Industries, LP recalled 684 medical convenience kits on January 7, 2026. The recall affects the LVAD Driveline Tray and the KIT Surg Onc Insert Cent. Venou due to calibration issues impacting sterility. Health providers and patients should stop using these products immediately.
Olympus Corporation recalled 4,183 units of the Single Use 3-Lumen Sphincterotome V on January 7, 2026. Devices may deform and lose performance due to inadequate thermoforming. Healthcare providers should immediately stop using the affected products and follow recall instructions.