1,003 recalls tagged with “chemical hazard”.
Fujirebio Diagnostics recalled 179 units of Lumipulse ¿-Amyloid Plasma Controls on December 11, 2025. The recall stems from inaccurate test results leading to potential misclassification of Alzheimer's disease. Customers should stop using the device immediately and follow the manufacturer's instructions.
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.
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 two pound cake products on December 11, 2025, due to undeclared soy. Consumers with allergies to soy are at risk of serious allergic reactions. A total of 61 cakes were shipped to Virginia and West Virginia.
Fujirebio Diagnostics recalled 23 units of its Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio test on December 11, 2025. The recall follows concerns that the product may produce inaccurate test results, potentially misclassifying patients with Alzheimer's disease. Healthcare providers should stop using this device immediately and follow recall instructions.
Fujirebio Diagnostics recalled 128 units of Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators on December 11, 2025. The recall stems from the risk of inaccurate test results leading to misclassification of Alzheimer’s disease. Affected products may cause patients to receive unnecessary additional clinical testing.
Fujirebio Diagnostics recalled 1,569 units of Lumipulse G pTau 217 Plasma Immunoreaction Cartridges on December 11, 2025. The recall affects users due to potential inaccurate test results associated with Alzheimer's disease classifications. Customers in 13 states should stop using the product immediately.
Fujirebio Diagnostics has recalled 117 units of Lumipulse G pTau 217 Plasma Calibrators due to inaccurate test results. The recall was announced on December 11, 2025, after customers reported false classifications of Alzheimer’s disease. Affected products were distributed nationwide, including in states like California and Florida.
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.
Intuitive Surgical recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.
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+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.
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.
ORL Labs recalled 1,458 containers of ORL Kids Natural Toothpaste, Bubblegum Flavor, on December 8, 2025. The recall follows cGMP deviations that could pose health risks. Consumers should stop using the product immediately.
Beckman Coulter recalled 34,451 units of its LDL Cholesterol OSR6x96 assay on December 8, 2025, due to significant performance interference. The recall affects multiple states in the U.S. and several countries internationally. Affected products may provide inaccurate LDL cholesterol readings, posing health risks to patients.
ORL Labs, LLC recalled 570 bottles of ORL Kids Mouthwash, Bubblegum Flavor on December 8, 2025. The recall stems from violations of current Good Manufacturing Practices (cGMP). The product was distributed only in Arizona and poses potential safety risks for children.
Keurig Green Mountain recalled 960 cartons of McCafe Premium Roast Decaf Coffee K-Cup Pods on December 6, 2025. The product is inaccurately labeled as decaf but may contain caffeine. Consumers in CA, IN, and NV should not consume the pods and seek refunds.
Fresh & Ready Foods recalled 278 units of Spicy Veggie Breakfast Burrito on December 5, 2025. The recall occurred due to foreign material found in the product. Consumers should not eat the burrito and should seek a refund or replacement.
Fresh & Ready Foods recalled 93 units of Spicy Breakfast Burrito on December 5, 2025, due to foreign material contamination. The burritos were sold in Oregon and Washington. Consumers should not eat the product and seek refunds or replacements.
Fresh & Ready Foods recalled 200 units of its Evergreen Refreshments brand Ready to Eat Tacos on December 5, 2025. The product may contain foreign material posing a health risk. Consumers should not eat the product and seek a refund.