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.
Hino is recalling one 2021 NJ8A vehicle because air brake hose fittings may lack required manufacturer markings, potentially increasing crash risk.
Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.
Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.
Ferrara Fire Apparatus is recalling 2019-2022 Inferno, Cinder, and Igniter vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.
Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.
Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.
Dream Pops 100% Plant-Based Birthday Cake Bites are being recalled because they contain undeclared milk, a known allergen that poses a risk to people with milk allergies.
Dream Pops 100% Plant-Based Cookie Dough Bites are being recalled because they contain undeclared milk allergen. The product was distributed nationwide in the US and Canada.
Exela Pharma Sciences is recalling 8.4% Sodium Bicarbonate Injection due to lack of assurance of sterility. The affected lot (C0001088/P0001317, expiring 08/2023) was distributed nationwide.
Vee Tyre is recalling specific Tri-Ace Pioneer A/T III tires because the sidewall may separate, increasing the risk of a crash.
Taro Pharmaceuticals is recalling Clobetasol Propionate Ointment USP 0.05% due to the presence of R. Pickettii bacteria in a non-sterile product. The affected lot may have been distributed nationwide through retailers.
Getinge Usa Sales Inc recalls Vaporizer Sevoflurane components in anesthesia systems due to potential chemical degradation that may cause hydrogen fluoride exposure via inhalation or skin contact.
Dream Pops 100% Plant-Based Vanilla Sky Bites are being recalled because they contain undeclared milk, a common allergen that may pose a health risk to consumers with milk allergies.
Dream Pops is recalling 100% Plant-Based Dream Pops Berry Dreams Bites due to undeclared milk allergen. The product was distributed nationwide in the US and Canada with Best By dates from 6/28/22 to 10/21/22.
Joseph Seviroli Inc. is recalling Aplenty Rotini with Plant Based Bolognese Meal Kit due to the potential presence of undeclared milk. This product may pose a risk to consumers with milk allergies.
Philips wireless footswitches used with Allura Xper and Azurion X-ray systems may experience connection issues that interrupt fluoroscopic imaging during patient procedures. The recall affects 1,971 systems distributed worldwide.
Medtronic is recalling approximately 6,653 Custom Perfusion kits used in cardiac procedures because they were labeled as non-pyrogenic without completing required endotoxin testing.
Siemens SOMATOM Edge Plus CT systems running software version VB20_SP5 may produce degraded head images, potentially leading to patient misdiagnosis.
Mushie & Co is recalling about 333,725 FRIGG Silicone Pacifiers because the silicone nipple can detach from the plastic shield, posing a choking hazard. Eight detachments have been reported in the U.S. with no injuries.
Haag-Streit OCT-Camera devices with automatic laser shut-off malfunction may fail to recognize when the laser is safely switched off, posing a potential safety risk.
Childrensalon is recalling about 180 children's sleepwear garments that fail to meet U.S. flammability standards, posing a burn injury risk. Consumers should stop using the garments immediately and contact Childrensalon for return instructions.
Siemens SOMATOM Confidence CT scanners with software version VB20_SP5 may experience degraded head image quality, creating a potential risk of misdiagnosis. The recall affects 108 units distributed nationwide.
Canon Medical's flat panel detectors used in Alphenix surgical systems may display abnormal horizontal stripes and fail to recover by restarting, potentially causing operators to work without proper visual guidance during procedures.
DePuy Orthopaedics is recalling GLOBAL UNITE STD STEM orthopedic implants due to undersized spigot bore diameter that may prevent proper removal during revision surgery, risking surgical delay and bone damage.