2,755 recalls tagged with “immediate action”.
Made Fresh Salads recalled 557 tubs of Vegetable Cream Cheese sold in New York after a potential Listeria monocytogenes contamination. The recall covers all expiration dates through 02/27/2026. Consumers who bought this product should not eat it and should contact Made Fresh Salads Inc for refund or replacement by telephone.
Made Fresh Salads recalled 557 five‑pound tubs of Walnut Raisin Cream Cheese distributed in New York after identifying a potential Listeria monocytogenes contamination. The product is a Walnut Raisin Cream Cheese in a 5‑pound white plastic tub. Consumers who bought this product should not consume it and should contact Made Fresh Salads Inc for refunds or replacements by telephone.
Made Fresh Salads recalled 557 five-pound Apple Cinnamon Cream Cheese tubs distributed in New York after an FDA enforcement report due to Listeria monocytogenes contamination. The contamination poses a risk of serious illness if consumed. Consumers should not eat the product and should contact Made Fresh Salads Inc for refunds or replacements by telephone.
Prismatic 3D Prints recalled Book Nooks on February 19, 2026, due to a significant risk of battery ingestion. The decorative bookshelf items can be accessed by children, exposing them to dangerous lithium coin batteries. Consumers must stop using the product and follow safety guidelines immediately.
Made Fresh Salads recalled 557 five-pound tubs of Lox Cream Cheese due to possible Listeria monocytogenes contamination. This contamination poses serious health risks, especially to vulnerable groups. Consumers should not eat this product and should contact Made Fresh Salads for a refund.
Made Fresh Salads recalled 557 tubs of blueberry cream cheese after testing revealed contamination with Listeria monocytogenes. The product, sold in 5 lb white plastic tubs, poses a high risk of foodborne illness. Consumers should not consume this product and should contact Made Fresh Salads Inc for a refund immediately.
Made Fresh Salads Inc recalled 557 five-pound tubs of Garlic & Herb Cream Cheese sold in New York after a confirmed Listeria monocytogenes contamination. The recall was activated on February 19, 2026 and remains active as of March 18, 2026. Consumers who purchased the product should not consume it and should contact the company for refund or replacement guidance.
Made Fresh Salads recalled 557 five-pound tubs of Caramel Apple Cream Cheese due to potential Listeria monocytogenes contamination. This contamination can lead to serious infections, particularly in vulnerable populations. Consumers should stop using the product and contact Made Fresh Salads for a refund.
Huaker recalled its Magnetic Balls and Rods sets on February 19, 2026, due to a choking risk for children. The 88-piece sets are intended for children under three years old and violate safety standards. Consumers must stop using the product immediately and return it for a full refund.
JJGoo recalled LED balloon lights on February 19, 2026, due to a serious ingestion hazard from button cell batteries. The recall affects approximately 100,000 units sold in packs of 100. Consumers should stop using the lights immediately and seek a refund.
Joly's LLC recalled 80% Vinegar on February 19, 2026, due to serious risks of poisoning and chemical burns. The product lacks essential warning labels and first aid instructions, violating federal safety laws. Consumers should stop using the product immediately and seek a refund.
Meijer recalled several styles of children's sleepwear on February 19, 2026, due to a burn hazard. The recall affects various one-piece footed sleepwear for infants sizes 12, 18, and 24 months. Consumers should stop using the sleepwear and return it for a full refund.
Vive Health recalled adult portable bed rails on February 19, 2026, due to serious entrapment risks. The recall affects models LVA1024 and LVA3031BLK. Consumers must stop using the product immediately and contact Vive Health for a full refund.
SAMIT recalled multi-purpose helmets for children on February 19, 2026. The helmets fail to meet safety standards, posing a risk of serious injury or death. Consumers should stop using them immediately and seek a refund.
Sunflour Bakery recalled 1 bag of Hamburger Bun, 18oz with six buns sold to a single Orange County retailer. The recall involves sesame seeds not declared on the label. Consumers should not eat the product and should contact Sunflour Bakery by email for refund or replacement.
Baxter Healthcare recalled 19 Blue Ventilator Adapter Modules used with the Volara Respiratory Therapy system in Florida after an urgent correction flagged potential oxygen desaturation and barotrauma risks in home care. The correction provides home caregiver instructions for use. Patients and healthcare providers should stop using this device immediately and contact Baxter or a healthcare provide
Navajo Manufacturing recalled 28,457 Handy Solutions Neck & Shoulders Heating Pads sold nationwide through Multiple Retailers. The defect allows overheating if the pad is folded or placed under the body, and the high limit device may fail to shut off. Stop use and contact Navajo Manufacturing for instructions.
Medline Industries recalled 420 Sterile Radiology Procedure Kits, Model DYNDH1491B, distributed nationwide in Minnesota after a potential breach in sterile pouch packaging. The defect may compromise product sterility. Stop using the kit immediately and contact Medline or your healthcare provider for instructions.
Abiomed has issued a Class I recall for 33,107 Purge Cassette units used with Impella pump sets worldwide due to purge leaks in Generation 1 cassettes. The leaks raise the risk of compromised device performance. Patients and healthcare providers should stop using the affected devices immediately and follow Abiomed's recall instructions.
Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.