State
73,388 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 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pacific Cycle is recalling about 11,340 Schwinn Tone electric scooters because the handlebar grips can loosen or crack, causing falls and injuries. One consumer fell and sustained bruising and abrasions when the handlebar broke during use.
Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a software error may allow the vehicle to move while in Park.
Hisun Motors is recalling about 2,500 Sector 250cc and RK Performance 250cc utility vehicles sold at Rural King stores nationwide from November 2014 through June 2021 because grass can accumulate near the exhaust pipe and pose a fire hazard. The company has received five reports of vehicle fires but no injuries.
Philips has recalled BV Pulsera mobile X-ray systems due to missing temperature specifications in the instructions for use. The X-ray tank and image intensifier lack maximum surface temperature documentation, creating a burn hazard.
Argon Medical Devices is recalling 79,910 SuperCore Biopsy Instruments due to housing and plunger components detaching from the semi-automatic devices. The devices were distributed worldwide and throughout the United States.
Conagra Brands is recalling Birds Eye Broccoli Tots (12 oz bags) due to the presence of small rocks and metal fragments in the product. Consumers should not eat the product and should dispose of it or return it.
Bentley is recalling certain 2021-2022 vehicles because the owner's manual incorrectly states the airbag will not deploy when the Passenger Airbag On symbol is illuminated. This could cause unsafe positioning during a crash.
Philips BV Endura diagnostic X-ray systems lack specifications for maximum surface temperatures in their instructions, creating potential for burn injuries.
Philips Veradius Unity diagnostic X-ray systems lack required temperature specifications in instructions, creating burn risk. Affected systems should not be used until updated documentation is received.
Orchestrate Orthodontic Technologies recalls O3D ORCHESTRATE user documentation because the labeling was altered from its FDA-approved version. Approximately 127 copies were distributed to practitioners worldwide.
Dr. Reddy's Laboratories is recalling 5,016 cartons of Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg Extended Release Tablets nationwide due to failed dissolution specifications. Affected lot is AC2103329F with expiration 1/2023.
About 77,900 Harbor Breeze Belleisle Bay and Honeywell Rio ceiling fans are recalled because the blades can detach during use and strike consumers or cause property damage.
Dr. Reddy's Laboratories is recalling Allergy and Congestion (Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg) Extended-Release Tablets because they failed to meet dissolution specifications. Approximately 4,896 cartons distributed nationwide are affected.
Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg Extended Release Tablets because they failed dissolution specifications, which may affect how the medication works in the body.
Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets distributed by Rugby Laboratories due to failed dissolution specifications. Affected lot AC2103329D (Exp 1/2023) was distributed nationwide in 2,184 cartons.
Dr. Reddy's Laboratories is recalling Walmart brand Allergy Relief D extended-release tablets (Lot #AC2103329B) nationwide because the tablets failed to meet dissolution specifications, which may affect medication effectiveness.
Ascent Pharmaceuticals is recalling Hydrocodone Bitartrate and Acetaminophen 10 mg/325 mg tablets nationwide due to a product mix-up. The recall affects 9,744 bottles and was voluntarily initiated by the manufacturer.
CVS Allergy Relief D extended-release tablets (Fexofenadine HCl 60 mg / Pseudoephedrine HCl 120 mg) are being recalled because they failed dissolution specifications, meaning the tablets may not release the medication properly.
Dr. Reddy's Laboratories is recalling Fexofenadine HCl 60 mg and Pseudoephedrine HCl 120 mg extended-release tablets because they failed to meet dissolution specifications, which may affect how the medication works in the body.
Dr. Reddy's Laboratories is recalling CVS Allergy & Congestion Relief tablets (fexofenadine HCl 60 mg/pseudoephedrine HCl 120 mg extended-release) nationwide due to failed dissolution specifications.
Dr. Reddy's Laboratories is recalling a 12 HR Allergy & Congestion Relief product distributed nationwide because the tablets failed to meet dissolution specifications, which may affect drug effectiveness.
Smithfield Packaged Meats is recalling approximately 10,990 pounds of Margherita pepperoni due to possible Bacillus cereus contamination. No illnesses have been reported.
Lion Electric Company is recalling 2017-2021 LionC school buses because a 12V circuit breaker switch may fail, causing a loss of braking and steering assist.
BorgWarner is recalling specific Delphi Aftermarket Tie Rod assemblies because the inner tie rod may detach, potentially causing a loss of steering control.
Tourig is recalling one 2017 Mercedes-Benz Sprinter motorhome because excessive voltage may damage components, increasing the risk of a fire.