These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
3,615 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The product poses a risk of Clostridium botulinum contamination. Consumers should not consume the product and should seek a refund.
Medartis AG recalls 126 APTUS 2.8 TriLock Screws 16mm HD7 worldwide. The mix-up between 2.5mm and 2.8mm outer diameter screws could affect fixation. Stop using the device and follow manufacturer recall instructions for disposition.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The product may be contaminated with Clostridium botulinum, which poses serious health risks. Consumers should stop using the product immediately and contact the company for a refund.
Diva Fam Inc recalled 5.4 million jars of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers are urged not to consume the product and seek refunds immediately.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. The affected product was sold nationwide and online. Consumers should not consume the gel and should seek refunds or replacements.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall follows potential contamination with Clostridium botulinum, a dangerous toxin. Consumers should not consume the product and seek refunds or replacements immediately.
Volkswagen recalled 2025 Tiguan vehicles after a rear tie rod bolt may loosen, risking loss of vehicle control. Dealers will replace the bolt at no charge under recall 42E7. Letters were mailed Sept. 5, 2025.
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.
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.
Island Crab Corporation recalled 23 units of Smoked Grouper Dip on January 8, 2026. The product contains undeclared allergens including milk, eggs, and sodium metabisulfite. Consumers should not consume this product and seek a refund.
Kalencom Corporation recalled SARO Braided Crib Bumpers on January 8, 2026, due to suffocation risks. The bumpers can obstruct an infant's breathing, violating federal safety regulations. Consumers should stop using the product immediately and seek a refund.
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.
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.
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.
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.
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 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.
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.
YOLAAH recalled its portable bed rails on January 8, 2026, due to serious safety hazards. The recall affects model BR-01, which presents an entrapment risk that could lead to asphyxiation. Consumers should stop using the product immediately and seek a refund.
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.