2,228 recalls tagged with “stop use immediately”.
Encore Medical, LP recalled 20 shoulder prosthesis implants on January 15, 2026. Incorrect labeling on the RSP Standard Humeral Socket Insert poses a high hazard risk. Affected products were distributed nationwide across multiple states.
Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.
Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.
Medline Unna-Z Stretch Zinc Paste Bandage faces a high-risk labeling error. The recall covers 35,328 units distributed in the U.S. and other regions. Manufacturers warn to stop use immediately and follow recall instructions.
RootStim recalled Beard Growth Serum on January 15, 2026, due to inadequate child-resistant packaging. The product poses a serious poisoning risk to children. Consumers should stop using it immediately and secure it out of reach.
Ruahouine recalled its Hair Growth Serum on January 15, 2026, due to a poisoning hazard. The product lacks child-resistant packaging, violating safety standards. This poses a risk of serious injury or death if ingested by children.
HEZI recalled power strips on January 15, 2026, due to an electrocution hazard. The power strips have an ungrounded metal enclosure that can become energized. Consumers should stop using them immediately and seek a refund.
Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.
R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.
Curtis International recalled 50,000 Frigidaire-brand minifridges on January 15, 2026, due to fire and burn hazards. The recall affects model EFMIS121 and previously recalled models EFMIS129, EFMIS137, EFMIS149, and EFMIS175. Consumers should stop using these minifridges immediately and seek a refund.
Greatale recalled self-feeding pillows on January 15, 2026, due to a serious risk of aspiration and suffocation in infants. The pillows can hold a bottle at an unsafe angle, preventing infants from pulling away. Consumers must stop using the pillows immediately and return them for a full refund.
Greenstone LLC recalled 3,456 cartons of methylprednisolone tablets on January 15, 2026. The recall follows reports of incorrect dosing information due to misapplied blister foil. Consumers should stop using the product immediately and contact their healthcare provider.
Aonic Inc. recalled 3,630 bottles of Aonic Complete Hers dietary supplement on January 15, 2026. Possible contamination with coliforms, E. coli, and Pseudomonas aeruginosa prompted the recall. Consumers in Utah should stop using the product immediately.
LUBNA QUALITY PRODUCTS recalled 400 cases of mung beans on January 15, 2026, due to the presence of Thiamethoxam, a pesticide. The affected products were distributed in Texas and Louisiana. Consumers should not consume the product and should seek refunds or replacements.
Encore Medical, LP recalled 14 EMPOWR 3D Knee implants on January 15, 2026. The implants contain incorrect labeling that poses a risk to patients. Healthcare providers should stop using the device immediately and follow recall instructions.
Rose and Shore recalled 5,067.1 cases of 14" Margarita Thin Crust Pizza sold at a single regional chain in California, Oregon, Arizona, Idaho and Texas. A potential foreign object has been found in tomatoes used in the product. Consumers should not eat this pizza and should contact Rose and Shore for refund or replacement by email.
Sevillo Fine Foods recalled 520 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina after the product may contain metal fragments. The product is frozen and packaged in bulk with a plastic liner inside a cardboard box. Consumers should not eat the product and should contact Sevillo Fine Foods for refund or replacement via email.
Sevillo Fine Foods recalled 2,372 units of Slow Roasted Diced Tomatoes distributed to California and North Carolina. The product may contain metal fragments. Consumers should not consume the product and should contact Sevillo Fine Foods for refunds or replacements.
KVK-Tech Inc. recalled 31,676 packages of Oxycodone Hydrochloride Tablets on January 14, 2026. Defective seals may cause tablets to fall out, posing a health risk. Customers should stop using the product immediately and seek guidance from healthcare providers.
Edermy LLC recalled 11,202 medical devices on January 14, 2026. The recall affects models P2HC-A, P2HC-S, and P2HC due to lack of proper FDA clearance. Patients and healthcare providers should immediately cease use of these devices and follow recall instructions.