1,862 recalls tagged with “stop use immediately”.
Mei Heong Yuen Garlic Flavor Roasted Peanuts, distributed by Super World Trading Inc., were recalled on Feb. 19, 2026. The products contain cyclamates, a banned sweetener. Consumers who purchased the product should not consume it and should contact the distributor for refund or replacement.
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 Walnut Flavor Roasted Peanuts recalled in the United States by Super World Trading Inc. on Feb. 19, 2026. The product contains cyclamates, a banned sweetener. Consumers should not eat this product and should contact the distributor for refunds or replacements.
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.
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.
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.
Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.
Mentor Texas, LP recalled Artoura Breast Tissue Expanders sold worldwide, including the United States. The infusion sets may contain a dull or blunt needle tip, which may be difficult to advance or break. Healthcare providers and patients should stop using the affected devices and await recall instructions by letter.
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.
Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including the US. Infusion sets may have a dull or blunt needle tip that is difficult to advance or may break. Patients and healthcare providers should stop using the device immediately and contact Mentor Texas, LP for instructions.
Mentor Texas, LP recalled Artoura Breast Tissue Expanders worldwide after discovery of dull infusion needle tips. The issue may make it difficult to advance the infusion set or cause it to break. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.
HTO Nevada Inc. dba Kirkman recalled 243 bottles of MAXIMUM ZONE 2, 4% lidocaine cream distributed nationwide by Dermal Source. The recall cites stability data that does not support an expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.