2,142 recalls tagged with “cpsc regulated”.
Radnostix recalled 2,699 gelatin capsule packs used with its Sodium Iodide I-131 kit, distributed nationwide in the United States and Puerto Rico. The capsules failed to meet tablet/capsule specifications. Healthcare providers and patients should stop using the product and contact Radnostix for guidance.
AMO Puerto Rico Manufacturing recalls 361 TECNIS Eyhance IOL with TECNIS Simplicity Delivery System lenses sold nationwide through healthcare providers. The lenses may have a haptic that sticks to the optic, preventing unfolding as expected. Patients and clinicians should stop using the device immediately and follow recall instructions.
Mei Heong Yuen Tangerine Flavor Roasted Peanuts, distributed in the United States by Super World Trading Inc., are recalled across 595 cases under H-0641-2026. The product contains cyclamate, a banned sweetener. Consumers should stop consuming the product and contact the distributor for refunds or replacements.
Made Fresh Salads recalled 557 five-pound tubs of Tofu Whipped sold in New York after an FDA notice identified possible Listeria monocytogenes contamination. The recall cites a risk to consumer safety. Consumers who bought the 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 white plastic tubs of whipped cream cheese distributed in New York after FDA enforcement cited possible Listeria monocytogenes contamination. All expiration dates through 2026-02-27 may be affected. Consumers should not consume the product and should contact Made Fresh Salads Inc for refund or replacement information by telephone.
Made Fresh Salads recalled 557 five-pound tubs of Strawberry Cream Cheese after a Listeria monocytogenes contamination was identified. The recall covers all expiration dates through 2/27/2026 and distribution is limited to New York. Consumers should not consume the product and should contact Made Fresh Salads Inc by telephone for refund or replacement.
Made Fresh Salads recalled 557 five-pound tubs of Jalapeno Cheddar Cream Cheese sold in New York after FDA notice of Listeria monocytogenes contamination. The recall date is 2026-02-19 and the status remains ACTIVE. Consumers should not consume the product and should contact Made Fresh Salads Inc for refund or replacement information by telephone.
Made Fresh Salads Inc. recalled 557 five-pound tubs of Scallion Cream Cheese in New York on February 19, 2026. The recall cites possible contamination with Listeria monocytogenes. Consumers who bought the product should not consume it and should contact Made Fresh Salads for refunds or replacements.
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 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