527 recalls tagged with “adult product”.
Ukrop's Homestyle Foods recalled 61 units of 6" Pound Cake on December 11, 2025. The product contains undeclared soy, posing a high risk to those with soy allergies. Affected cakes were shipped to Virginia and West Virginia.
Ukrop's Homestyle Foods recalled 61 units of its 6" Pound Cake on December 11, 2025. The product contains undeclared soy, posing a risk to those with soy allergies. The cakes were distributed to Virginia and West Virginia.
Fujirebio Diagnostics recalled 148 units of Lumipulse pTau 217 Plasma Controls on December 11, 2025. The recall follows reports of inaccurate test results that misclassify patients regarding Alzheimer’s disease. The affected product may falsely elevate positive or indeterminate results, increasing the risk of incorrect patient classification.
TREK recalled Model Year 2026 electric bicycles on December 11, 2025. The recall affects Domane+ ALR 5, Domane+ ALR 6 AXS, Checkpoint+ SL 6, and Checkpoint+ SL 7 models. Loose chainring bolts may cause falls or crashes, posing a risk to users.
Publix recalled 811 cases of Raspberry Coffee Cake on December 10, 2025. The product contains undeclared walnuts, posing a serious allergen risk. Consumers should not consume the product and seek a refund.
Heraeus Medical GmbH recalled PALACOS MV+G pro 40 and MV+G pro 80 bone cement on December 9, 2025. The recall follows complaints about ampoule breakage, which can prevent proper cement formation. This issue could jeopardize patient safety during medical procedures.
Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.
Hyundai Motor America recalled 2025 Palisade vehicles due to faulty seat belt buckles. The defect affects driver, passenger, and second-row seats, increasing injury risk. Owners will receive notification letters by November 10, 2025.
Intuitive Surgical recalled 7,819 units of the da Vinci S/Si Mega Needle Driver Instrument sold worldwide to hospitals and healthcare providers. The recall cites broken or frayed grip cables that can impair instrument control. Stop using the device and follow the manufacturer’s recall instructions for replacement or service.
Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.
Intuitive Surgical recalled 2,370 units of the da Vinci S, Si Double Fenestrated Grasper Instrument distributed worldwide on December 9, 2025. The EndoWrist instruments use mechanical cables to transmit motion. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.
IMRIS Imaging recalled 122 Head Fixation Devices on December 8, 2025. A torque screw may crack or separate, posing serious risks during surgical procedures. Healthcare providers must stop using the device and follow recall instructions immediately.
Chrysler is recalling certain 2024-2025 Dodge Charger vehicles due to a software issue. The amplifier may not emit necessary exterior sounds, increasing crash risks. Owners were notified by mail on June 26, 2025.
Ningbo Tianqi Electronic recalled FUFU&GAGA Murphy wall beds on December 4, 2025. The 215-pound frame can fall, posing impact and laceration hazards. Consumers should stop using the beds and seek refunds immediately.
Lil' Turtles recalled 110 cases of Grandma Belle's Tomato Basil Soup on December 4, 2025. The product contains undeclared milk, posing a risk to consumers with milk allergies. Consumers should stop using the soup and contact the manufacturer for a refund.
Primark US recalled water balloon pumps on December 4, 2025, due to a risk of injury. The pumps can generate excessive pressure, causing rupture during use. Consumers should stop using the product immediately and seek a refund.
Zimmer recalled 24 Affixus Antegrade Femoral Nails on December 2, 2025, due to a risk of implant fatigue fracture. Affected implants may cause serious health issues, including tissue damage and pain. Healthcare providers must stop using the device immediately and follow recall instructions.
Zimmer, Inc. recalled 23 Affixus Antegrade Femoral Nails on December 2, 2025. These implants may have an undersized distal diameter that could lead to fatigue fractures. Patients should stop using the device immediately and contact their healthcare provider.
Zimmer recalled 11 Affixus Antegrade Femoral Nails on December 2, 2025. Affected implants may fracture, leading to serious health risks. Patients should stop using the device immediately and follow manufacturer instructions.
Affixus recalled its Antegrade Femoral Nailing System on December 2, 2025, due to a potential implant fatigue fracture risk. The recall affects 22 units distributed nationwide in 14 states. Patients should stop using the affected devices immediately to avoid serious health risks.