State
73,827 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 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 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mohawk Industries is recalling Altitude Gold shag rugs sold at The Home Depot because large sizes fail federal flammability standards, posing fire and burn risks.
American Medical Systems is recalling AMS 700 Series Accessory Kits because supplier-supplied Keith needles may bend or break when used with the Furlow tool.
Olympus is recalling DS-5500 digital audio recorders because they can overheat while charging, posing a burn hazard to consumers and property.
Mondelez Global LLC is voluntarily recalling Chiclets Gum because the label fails to declare soy lecithin, a common allergen.
Toyota is recalling specific models because seat cushion compression may damage heater wiring, creating a fire and injury risk.
Hoppe's is recalling Semi-Auto Gun Bore Cleaner bottles because the child-resistant caps can become loose, posing a risk of chemical ingestion.
DePuy Orthopaedics is recalling ATTUNE Intuition Distal Femoral Jigs because a pin bushing defect could cause the plastic to fracture or displace during use.
AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.
Siemens is recalling 164 Artis zeego systems because a cable may be routed incorrectly, potentially causing system failure during procedures.
Masimo Corporation is recalling specific SET uSpO2 Pulse Oximetry Cables due to crossed internal wires that may cause the monitoring device to display inverted SpO2 values.
GE Healthcare is recalling 478 nuclear medicine imaging devices because loose fasteners could cause a portion of the system to fall onto a patient during a scan.
Integra LifeSciences Corp. is recalling 12 units of Reverse Shoulder System cutting templates because the threaded handle was welded backwards, resulting in an incorrect cutting angle.
Mondelez Global LLC is voluntarily recalling Chiclets Chewing Gum because the label fails to declare soy lecithin, a common allergen.
GE Healthcare is recalling 22 Brivo NM615 nuclear imaging systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.
Mondelez Global LLC is voluntarily recalling Chiclets Peppermint Gum because the label fails to declare soy lecithin, a common allergen.
GE Healthcare is recalling 147 Discovery NM 630 nuclear imaging systems to update maintenance procedures and prevent loose fasteners from causing parts to fall on patients.
Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.
Mondelez Global LLC is voluntarily recalling Chiclets Assorted Variety Multipak fruit flavor gum due to undeclared soy lecithin on the label.
China Manufacturers Alliance is recalling specific Bluestar trailer tires that may develop sidewall blisters, potentially causing loss of vehicle control.
Fougera Pharmaceuticals is recalling specific lots of Fluocinonide Gel USP, 0.05% because they may not meet USP requirements for residual solvents.
Contract Packaging Resources Inc. is recalling Assured Naproxen Sodium Tablets because correct labeled bottles of Assured Ibuprofen softgels were mistakenly packaged into Naproxen cartons.
Maquet Cardiovascular is recalling 331 Cardiohelp-I Systems due to a software issue that may display an erroneous 'Battery Needs Service' message after startup.
Zimmer, Inc. is recalling 138 units of Persona Stemmed 5 Degree Cemented Tibia knee components due to a cleaning process validation failure.
Fresenius Kabi is recalling Haloperidol Decanoate Injection vials due to an out-of-specification impurity result. The recall covers 216,517 vials distributed nationwide and in Puerto Rico.
City Line Foods is expanding a recall of 1.2 million pounds of frozen pretzel dog products due to misbranding and undeclared soy lecithin, a known allergen.