2,229 recalls tagged with “stop use immediately”.
Siemens Medical Solutions recalled software applications for certain CT systems on December 19, 2025. The applications did not receive FDA 510(k) clearance. Five units distributed worldwide are affected by this recall.
Novo Nordisk recalled Wegovy (semaglutide) injections on December 19, 2025, after discovering hair in prefilled syringes. The contamination poses a serious hazard to consumers. The recall affects all units distributed nationwide.
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.
Rifton Equipment recalled 470 E-Pacer gait training devices on December 18, 2025. The body support strap may fray, posing a risk to users. Health care providers and patients must stop using the device immediately.
Potential for fraying on the body support strap.
Presence of particulate matter - Glass like particles.
Imprimis NJOF, LLC recalled 596 boxes of intraocular injections on December 18, 2025. The recall affects products due to the presence of glass-like particles. Consumers should stop using the product immediately and contact their healthcare provider.
ANNQUAN recalled its power strips on December 18 after reports of fire hazards. The affected models are EX-D112-05 and EX-D106-25. Consumers should stop using these power strips immediately and seek a refund.
This recall involves the Fat Tire Trike, an aluminum adult three-wheeled electric tricycle. It has a rectangular label on the downtube near the front of the frame with the word "Pedego" printed on it. The product was sold in matte black.
Presence of particulate matter - Glass like particles.
Price Chopper recalled 3,290 cases of frozen raw shrimp on December 18, 2025. The shrimp may be contaminated with Cesium-137, a radioactive isotope. Consumers should stop using the product and seek refunds.
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
Potential for fraying on the body support strap.
Aju Pharm Co. recalled 1,088 units of its Fixone Biocomposite Anchor on December 17, 2025, due to serious device failures. Reports include anchor breakage, bending, and suture breakage. Healthcare providers and patients must stop using the device immediately.
Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage.