2,756 recalls tagged with “immediate action”.
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 5,438,998 jars of Sea Moss Gel on January 9, 2026 due to potential Clostridium botulinum contamination. Consumers should not consume the product and seek refunds or replacements. The recall affects various lot codes distributed nationwide.
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.
Medartis AG recalled the 2.5 TriLock Screw 16mm HD7, 1/Pkg, sold worldwide through medical distributors including the US states of Indiana and Pennsylvania. The recall stems from a mix-up between 2.5mm and 2.8mm outer diameter screws. Healthcare providers and patients should stop using the device immediately and follow manufacturer recall instructions.
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.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026. The recall stems from potential Clostridium botulinum contamination. Consumers should not consume the product and seek refunds immediately.
Diva Fam Inc recalled approximately 5.4 million jars of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. Consumers should not consume the product and are advised to seek refunds. The recall affects multiple lot codes sold nationwide.
Diva Fam Inc recalled 5,438,998 units of Sea Moss Gel on January 9, 2026, due to potential Clostridium botulinum contamination. The recall affects Soursop flavor products sold in glass jars. Consumers should stop using the product immediately and seek a refund or replacement.
FUJIFILM Healthcare Americas recalled 16 units of the CH-200 X-ray high-voltage generator on January 9, 2026. The electromagnetic contactors may weld, potentially causing overheating and smoke. The recall affects units distributed nationwide in various states including California and Florida.
Diva Fam Inc recalled 5,438,998 jars of Sea Moss Gel on January 9, 2026. The product may be contaminated with Clostridium botulinum, posing serious health risks. Consumers should not consume the product and seek refunds immediately.
Maquet Cardiopulmonary Gmbh recalled 3,050 Venous Bubble Sensors on January 9, 2026. Internal investigations revealed issues with the durability of the connecting cable. Excessive bending can lead to device failure, posing a risk to patient safety.
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.
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.
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.
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.
DR Power Equipment recalled walk-behind and tow-behind leaf vacuums after reports of laceration hazards. The recall affects multiple model numbers sold from September 2014 to June 2025. Consumers should stop using these vacuums immediately and seek repairs.