1,035 recalls tagged with “chemical hazard”.
Prima Foods International recalled 12,214 bottles of BarbaCuban 455 Everything Sauce on December 17, 2025. The sauce contains undeclared quinine, posing a health risk to consumers. Affected products were distributed in Florida with best by dates from January to June 2026.
Prima Foods International recalled 12,214 bottles of its 90 Miles to Mojo Marinade on December 17, 2025. The product contains undeclared quinine, posing a serious health risk. Consumers should not consume this product and should seek a refund immediately.
Rovira Biscuit Corporation recalled 6,671 units of Snack Crackers on December 17, 2025. The recall follows the discovery of undeclared FD&C Yellow #6 and FD&C Red 40 in the products. The affected crackers were distributed across several states, including Georgia and Texas.
Rovira Biscuit Corporation recalled 16,478 units of Vainilla Crackers on December 17, 2025. The recall occurred due to undeclared colors FD&C Yellow #6 and FD&C Red 40. Consumers should not consume the product and seek a refund or replacement.
ZIYAD Brothers Importing recalled 2,865 cases of French Style Puff Pastry on December 17, 2025. The product may contain partially hydrogenated oils, posing a health risk. Consumers should not consume the product and seek refunds immediately.
Rovira Biscuit Corporation recalled 29,246 units of Tita Crackers on December 17, 2025. The recall stems from undeclared colors FD&C Yellow #6 and FD&C Red 40. Consumers in GA, TX, MA, IL, MD, USVI, and Puerto Rico should not consume these products.
BarbaCuban recalled 12,214 bottles of White Truffle Sauce on December 17, 2025, due to undeclared quinine. The affected product poses a high risk to consumers. Customers should not consume the sauce and seek refunds immediately.
Rovira Biscuit Corporation recalled 71,492 units of Vanilla Treats Crackers on December 17, 2025. The product contains undeclared FD&C Yellow #6 and FD&C Red 40. Consumers should not consume the crackers and should seek refunds.
Rovira Biscuit Corporation recalled 9,838 units of Tempting Crackers Tray on December 17, 2025. The recall stems from undeclared colors FD&C Yellow #6 and FD&C Red 40. The affected products were distributed in several states, including Georgia and Texas, as well as Puerto Rico.
H-E-B recalled 175 cases of Higher Harvest Dairy Free Coconut Based Yogurt on December 17, 2025. The product contains undeclared almonds, posing a serious allergy risk. Consumers should stop using the yogurt immediately and contact the company for refunds.
Vortex Surgical recalled 14,789 Disposable Diamond Dusted ILM Elevators on December 16, 2025. The recall follows concerns about voids in the seal of Tyvek pouches, which could lead to bioburden contamination. Healthcare providers and patients should stop using the devices immediately.
Vortex Surgical recalled 14,789 surgical backflush pouches on December 16, 2025, due to compromised sterile barriers. The recall affects catalog numbers VS0270.25 and VS0275.27, with potential for bioburden contamination. Healthcare providers and patients should stop using these devices immediately.
Vortex Surgical recalled 14,789 Tecfen Retractable Membrane Polishers on December 16, 2025. The recall stems from potential voids in Tyvek pouches that may compromise sterility and lead to bioburden contamination. Healthcare providers and patients must stop using the products immediately.
Vortex Surgical recalled 14,789 I2 Injection Kits on December 16, 2025. Voids in the seal of Tyvek pouches may compromise sterility, posing an infection risk. Healthcare providers and patients must stop using this device immediately.
Vortex Surgical recalled 14,789 convenience kits on December 16, 2025, due to potential contamination risks. Voids in the seal of Tyvek pouches may compromise sterile barriers, leading to infection. Patients and healthcare providers should stop using these kits immediately.
Vortex Surgical recalled 14,789 disposable forceps and cannula on December 16, 2025, due to potential bioburden contamination. The recall affects various models distributed worldwide, including 8,651 in the U.S. and 6,138 internationally. Users should stop using these devices immediately to prevent infection risk.
Qunol recalled Extra Strength Turmeric Capsules due to mold contamination in raw materials. The recall affects over 3,000 units distributed across 27 states. Consumers should stop use and seek refunds immediately.
Alembic Pharmaceuticals Limited recalled Fesoterodine Fumarate, Extended-release Tablets after discovering high levels of a harmful impurity. The recall affects approximately 30,000 tablets distributed nationwide. Consumers must stop using the medication immediately and consult their healthcare providers.
SunMed Holdings recalled 20,583 units of Broselow Pediatric Emergency Rainbow Tape on December 15, 2025. The product contains harmful dosing errors for critical medications including Vecuronium, Flumazenil, and Ketamine. Healthcare providers and patients must stop using the tape immediately and follow recall instructions.
Immunotech A.S. recalled 160 Estrone RIA kits on December 15, 2025, due to a risk of falsely high patient results. This class II recall affects kits distributed in multiple countries, including the US and several European nations.