State
73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Howmedica Osteonics is recalling SCORPIO TS TIB INSERT knee replacement inserts manufactured with aging raw material. The material may develop elevated oxidation that could affect performance.
Howmedica Osteonics is recalling PS LIPPED TIBIAL INSERT ASSY DURACON knee replacement inserts manufactured with UHMWPE raw material over 5 years old. The aged material may develop elevated oxidation that could impact material properties.
Howmedica Osteonics is recalling PRIMARY REV.TIB.INSERT-DURACON knee replacement inserts manufactured with aging UHMWPE material that has potential for oxidation affecting material properties. Affected lots: 36273601 and 36609701.
Howmedica Osteonics has recalled certain SCORPIO U-Dome Patella knee implants due to potential material oxidation in units manufactured with raw material over 5 years old. The oxidation may affect the implant's material properties.
Medline recalls Blood Culture Kits because kit inserts fail to reflect the expiration date of included Bactec components. Users could unknowingly use expired components if they don't independently check the Bactec label.
Medline recalls Adult Blood Culture Trays due to incomplete documentation of Bactec component expiration dates on kit inserts. Users should verify the component expiration date before use.
Aesculap Inc is recalling 53 JACOBSON DUROGRIP TC micro needle holders that were shipped with incorrect product labels, which may cause delays during surgical procedures.
Den-Mat Holdings recalls Hydrogen Peroxide Oral Rinse products nationwide due to manufacturing deviations that may result in products not conforming to labeled specifications.
MICROVENTION is recalling TERUMO HydroPearl Compressible Microspheres because manufacturing and quality processes were not followed during production. The recall affects 22 units distributed in seven U.S. states.
Medline is recalling blood culture bottle kits with mismatched component expiration date documentation, creating risk of using expired components if not verified by users.
Terragene S.A. is recalling Terragene Bionova PCD (Model PCD222-C) medical devices nationwide due to a discrepancy between FDA-cleared instructions for use and the actual instructions distributed with the products.
Medline is recalling blood culture collection kits because the Bactec component expiration date is not documented on the kit insert. Users who do not check the component directly risk using an expired element.
JTEKT is recalling Electronic Power Steering Systems because improperly tightened bolts may cause the steering gear to lock up, resulting in a loss of steering control.
Mitsubishi Fuso is recalling 2024 Rizon FEC7K and FEC9K trucks because a control unit error may cause the vehicle to shut down unexpectedly, increasing crash risk.
Worldwide Distribution is recalling INGUSA/LP ASME Remote fill tanks because the liquid level remote fill gauge may leak in the open position, increasing fire risk.
Indian Motorcycle Company is recalling certain 2019-2022 Challenger, FTR 1200, and Pursuit motorcycles due to brake lights that may illuminate unexpectedly without rider input, potentially confusing following drivers and increasing crash risk.
Blue Bird is recalling 2021-2024 Vision school buses because a software defect may cause warning lights to turn off and the stop arm to retract unexpectedly.
Forest River is recalling 2023-2024 Salem and Wildwood fifth wheel travel trailers due to incorrect tire size information on their federal placards. This could lead to wrong tire installation and increased crash risk.
Mercedes-Benz is recalling 2019-2022 GLC 300, 2020 GLC 350e, and 2020-2022 AMG GLC 43 vehicles for headlights that may be incorrectly adjusted, creating glare for oncoming traffic. Dealers will correct the adjustment free of charge.
Nissan is recalling approximately 57,914 LEAF vehicles (2018-2022) where the rearview camera harness may become damaged, causing image distortion or loss and reducing rear visibility.
Gulf Stream is recalling 2024 Trail Boss 160FK trailers because the federal certification label lists incorrect tire size and pressure, which could lead to improper tire installation.
Huihuang Trading is recalling Fishing Games sold on Amazon.com from June through July 2023 because they contain magnets that exceed federal safety limits. Swallowed magnets can become lodged in the digestive system and cause serious injury or death.
DailySale Inc. is recalling its 216-piece 5mm Magnetic DIY Balls Magic Cube because the high-powered magnets violate federal toy safety regulations. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
Braun Ambulances is recalling 628 emergency vehicles from 2020-2024 because a wiring defect could cause electrical circuits to overheat and start a fire.
General Motors is recalling certain 2020-2024 Chevrolet Silverado and GMC Sierra pickup trucks due to faulty electronic tailgate switches that may inadvertently unlatch while the vehicle is parked. The defect can allow the tailgate to open while driving, potentially causing cargo loss and creating a road hazard.