State
73,363 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 177 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 30 (17%) are Severe.
Which agencies issued them
These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medicina Uk Ltd is recalling Medicina Reusable Oral Syringe 2.5ml units because plunger components were manufactured with polyethylene instead of the specified polypropylene material.
Medicina Uk Ltd is recalling Medicina Oral Tip Syringe 2.5ml nationwide because the plunger component was manufactured with polyethylene instead of the approved polypropylene material.
Abbott has recalled MitraClip G4 and TriClip G4 cardiac repair devices due to clip locking malfunctions that may prevent proper device deployment. These malfunctions could lead to failed procedures and serious complications including device embolization.
BALT USA is recalling Optima Coil System models OPTI0208CSS10 and OPTI0308CSS10 due to a labeling discrepancy where pouch labels do not match carton labels. These endovascular devices require verification before use.
Walgreens Sinus Pressure, Pain & Cough tablets are mislabeled as 'Decongestant Free' but contain Phenylephrine HCl, a nasal decongestant. The labeling error affects 66,384 boxes distributed nationwide.
Medicina Uk Ltd is recalling Medicina ENFit 5ml Reusable Enteral Syringes because the plunger component was manufactured with polyethylene instead of the specified polypropylene material.
Ingenus Pharmaceuticals is recalling Flunisolide Nasal Solution nationwide because the product contains impurities that exceed acceptable limits. The recall affects two lots distributed across the United States.
Golden State Medical Supply Inc. is recalling Rifampin Capsules, 150 mg, due to elevated levels of 1-Methyl-4-Nitrosopiperazine (MNP) exceeding the FDA interim specification limit of 5 ppm. Affected lots are distributed nationwide.
Porsche is recalling certain 2022 911 GT3 vehicles because the screw attaching the lower seat belt anchor may not have been properly tightened. A loose anchor could detach in a crash, increasing injury risk.
Clorox is recalling Pine-Sol cleaners contaminated with Pseudomonas aeruginosa, a bacteria that risks serious infection in immunocompromised people or those with external medical devices. No illnesses have been reported to date.
Gillig is recalling 388 2022 Low Floor transit buses because a steering shaft grease fitting may damage a protective shroud, potentially causing loss of steering control.
Kia is recalling 2008-2009 Sportage vehicles because an engine compartment fire may occur from the Hydraulic Electronic Control Unit, increasing injury risk.
CAN-AM is recalling 2019-2023 Ryker motorcycles because electrical harnesses in the front fenders may loosen and rub on the tire, causing a short circuit that can stall the engine while driving.
Altec is recalling 2019-2022 AT41ME aerial devices because the material handling interlocking valve may lose power, allowing the jib winch to operate while outriggers are up, which increases the risk of the unit tipping.
Autocar is recalling 2021-2023 Xpeditor vehicles because the steering column shaft pinch bolt may be improperly secured and bind, causing sudden loss of steering and increasing crash risk.
The guide bushing on the parking pawl may fatigue and prevent the parking brake from engaging, risking vehicle rollaway. Dealers will provide a free software update to affected 2019-2022 vehicles.
Tesla is recalling 2017-2022 Model 3 vehicles because second-row seat belt anchors may have been incorrectly reassembled during prior service work. Defective anchors could impair crash protection, increasing injury risk.
Thule is recalling certain Range, Camber 2, and Camber 4 bike carriers because a defective weld may cause the bike arm assembly to detach, increasing crash risk.
Winnebago Industries is recalling certain 2020-2023 View and Navion recreational vehicles. The LP fuel line is routed near the rear wheel well and may contact the tire, creating a fuel leak and fire risk.
Bob Evans Farms is recalling approximately 7,560 pounds of Italian pork sausage due to possible contamination with thin blue rubber.
Shyft Group is recalling 2023 Spartan K2 RV chassis because suspension fasteners may have insufficient strength, increasing crash risk.
Orange EV is recalling 2022 e-Triever vehicles because a loose parking brake fastener may prevent the brake from engaging, increasing the risk of a crash.
Ford is recalling certain 2023 E-450 vehicles because rear axle rotor bolts may be improperly tightened, risking wheel separation and increasing crash risk. Dealers will replace affected assemblies at no charge.
E-One is recalling 2022 Typhoon N, Cyclone II, and Cyclone N vehicles because improperly heat-treated tie rod clamps may crack, risking sudden loss of steering.
Gel Blaster is recalling about 62,700 SURGE Model 1.0 toy guns because the lithium-ion battery pack can overheat and ignite. Thirty reports of smoking or fire have been received with no injuries reported.