2,756 recalls tagged with “immediate action”.
Black Sheep Egg Company recalled 23,400 dozen Free Range Grade AA Large White Eggs sold at retail and wholesale locations in Arkansas and Missouri due to potential Salmonella contamination. Consumers should not eat these eggs. Contact Black Sheep Egg Company, LLC for refund or replacement information.
Black Sheep Egg Company recalled 46,800 dozen Free Range Grade AA Medium White Eggs sold at retail and wholesale outlets in Arkansas and Missouri. The FDA recall cites potential Salmonella contamination. Consumers should not consume the eggs and should contact Black Sheep Egg Company for refund or replacement.
Black Sheep Egg Company recalled 16,245 dozen Free Range Grade A Large Brown Eggs sold at retail locations in Arkansas and Missouri, and through wholesale brokers in Mississippi, Texas, California and Indiana. The cartons carry UPC 860010568538. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refunds or replacements.
Black Sheep Egg Company recalls 58,500 dozen free range Grade AA medium brown eggs after FDA enforcement notice citing potential Salmonella contamination. The recall covers eggs sold in Arkansas and Missouri, with wholesale and broker locations in Mississippi, Texas, California and Indiana. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refund or replacement.
Ascend Laboratories recalled Atorvastatin Calcium Tablets USP 40 mg, 90-count (NDC 67877-513-90), 500-count (NDC 67877-513-05), and 1,000-count (NDC 67877-513-10) nationwide in the United States. The batches failed dissolution specifications. Patients should stop using the medication and contact Ascend Laboratories, LLC or their healthcare provider for guidance.
Black Sheep Egg Company recalled Free Range Grade AA Large White Shell Eggs after Salmonella contamination concerns were identified. The recall covers 7,200 dozen eggs distributed to retail and wholesale locations in Arkansas and Missouri, with brokered sales in Mississippi, Texas, California and Indiana. Consumers should not consume these eggs and should contact the company for refund or refund/替
Arizer recalled the Solo II portable vaporizer on 2025-09-18 after reports of overheating lithium-ion batteries. The recall targets units imported by 7111495 Canada. Consumers should stop using the device and pursue a free replacement.
Youbeien recalled crib mobiles after multiple reports of battery ingestion risks. The mobiles can operate without a remote, but the battery compartment in the remote is easily accessible. Consumers should stop using the product and contact GKKBSJ for a full refund immediately.
IcyBreeze recalled the IcyBreeze Buddy portable misting fan due to a charging fire hazard. The recall affects consumers who own the IcyBreeze Buddy with a 1.5-liter water tank and a 10,000 mAh lithium-ion battery. Affected units must be returned for a full refund and disposal guidance. Call 817-900-2664 or visit the recall page to begin the process and receive a $150 credit at Solo Brands brands.
EnHomee recalled Fabric 13-Drawer Dressers sold directly by EnHomee Direct due to a tip-over and entrapment hazard. The units do not meet the STURDY Act mandatory standard. Consumers should stop using unanchored dressers and seek a full refund.
YooxArmor recalled its multi-purpose kids’ helmets sold on Amazon after safety violations. The helmets fail to meet the mandatory bicycle helmet standard for impact attenuation, stability, labeling and certification. Consumers should stop using the helmets and request a full refund from YooxArmor.
LXDHSTRA recalled baby loungers and crib bumpers on September 18, 2025. The recall covers LXDHSTRA-branded loungers sold online at Amazon. The defect involves suffocation and fall hazards linked to design and ban violations. Stop using immediately and seek a full refund from LXDHSTRA.
Five Below recalls two tabletop fire pits after reports of alcohol fuel flames jetting and spreading. The recall affects devices sold nationwide. Stop using the recalled pits immediately and contact Five Below for a refund. Full refunds available or $5 option; mail-back refunds possible with photo submission.
Taproom Gourmet bulk Park Mix, distributed to NY, NJ, CT, CA, IL and FL, is recalled for undeclared allergens and no ingredient label. Consumers should not consume the product. Egress Capital Partners Inc. is handling refunds or replacements via email.
B Braun Medical Inc. recalled 48,110 units of the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide to hospitals and surgical centers. The recall cites a potential for the lid of the catheter connector to be in the incorrect position. Hospitals and clinics should stop using the device and contact B Braun Medical for instructions.
B Braun Medical recalled the PERIFIX FX Continuous Epidural Anesthesia Tray nationwide. The recall centers on the lid of the catheter connector that may be in the incorrect position. Patients and healthcare providers should stop using the device immediately and follow recall instructions.
Cardinal Health 200, LLC recalls all lots of the Salem Sump Anti-Reflux Valve worldwide after complaints of valve breakage. The recall covers CE-marked valves with multiple identifiers. Hospitals and clinicians should stop using the device immediately and follow manufacturer instructions. This notice alerts providers to check for the affected code and act now.
GE Medical Systems recalled 31 LOGIQ P10 R4.5 HD ultrasound systems sold nationwide in the United States and globally after discovering UGAP measurements may misstate liver steatosis. The UGAP data may display inaccurate values representing liver steatosis. Healthcare providers and patients should stop using the device immediately and follow the manufacturer’s recall instructions.
Cook Medical recalled 695 Zenith Alpha 2 Thoracic Endovascular Grafts distributed to hospitals domestically and internationally. A defect could cause PTFE coating scrapings to be released during deployment, risking intravascular embolization. Healthcare providers and patients should stop using the device and follow the manufacturer’s recall instructions.
Taproom Gourmet brand bulk Broadway Mix recall covers 3,547 cases distributed across six states. The recall cites no ingredient label and undeclared allergens including peanuts, sesame, wheat and soy. Consumers should not consume the product and should seek refund or replacement through Egress Capital Partners Inc.