State

US Virgin Islands product recalls

73,495 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-10-14

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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24051–24075 of 73672

HighFDA (Devices)·Z-2166-2021·2021-08-04
Medical inflation device recalled due to handle separation risk
Merit Medical Systems is recalling basixALPHA Inflation Devices due to a design flaw where the syringe handle can separate when withdrawn, affecting device functionality.
Product
basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or other interventional device, and to measure the pressure within the balloon.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V604000·2021-08-04
Newmar Motorhomes Recalled for Potential Fuel Leak and Fire Risk
Newmar Corporation is recalling certain 2021-2022 motorhomes (New Aire, Ventana, and Dutch Star) with Cummins L9 diesel engines due to potential fuel leaks that could increase fire risk. Affected owners should contact Newmar customer service at 1-800-731-8300 for free fuel hose replacement.
Product
NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, VENTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2164-2021·2021-08-04
Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect
INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.
Product
Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V603000·2021-08-04
Lamborghini Recalls 2021 Urus for Rear Seat Belt Retract Defect
Lamborghini is recalling 2021 Urus vehicles because middle-rear seat belt retractors may deactivate early, preventing child restraints from securing properly.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2160-2021·2021-08-04
OEC 3D Imaging X-Ray Systems Recalled for Coin Cell Battery Depletion
GE OEC Medical Systems is recalling certain OEC 3D Imaging fluoroscopic X-ray systems due to potential premature depletion of the coin cell battery used to monitor X-ray tube temperature, which could cause the system to become inoperable.
Product
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2156-2021·2021-08-04
Affinity Four Birthing Bed Latch Mechanism Defect Poses Fall Risk
The latch mechanism on the Lift-Off foot section of certain Affinity Four Birthing Beds may be damaged, potentially causing improper engagement and creating a fall risk for patients. Hill-Rom is recalling approximately 1,096 affected beds.
Product
Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2162-2021·2021-08-04
Coaxial Interventional Needles Recalled for Potential Sterilization Defects
INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.
Product
Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V607000·2021-08-04
2021 Volkswagen ID.4 rear seat belt assemblies may not secure child restraints
Certain 2021 Volkswagen ID.4 vehicles have rear seat belt assemblies without proper automatic locking function, preventing child restraint systems from securing correctly. Dealers will inspect and replace affected assemblies at no cost.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2154-2021·2021-08-04
Daily Toric Contact Lenses Recalled for Misaligned Axis Mark
CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.
Product
SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2021·2021-08-04
Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision
CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.
Product
SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2021·2021-08-04
GE CARESCAPE PDM monitor SpO2 display freezes during extended use
GE Healthcare's CARESCAPE PDM-Masimo SpO2 physiological monitor displays can freeze after extended use without power down, preventing real-time oxygen saturation monitoring.
Product
CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2143-2021·2021-08-04
Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses with misaligned axis marks that may cause blurred vision. The defective lenses were distributed worldwide including multiple U.S. states.
Product
CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2147-2021·2021-08-04
CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.
Product
CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2145-2021·2021-08-04
Contact lens recall due to misaligned axis marking
CooperVision Inc. is recalling FRESH DAY 1 DAY TORIC contact lenses (Lot R0121629) due to misaligned axis marks that may cause blurred vision in wearers.
Product
FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2142-2021·2021-08-04
ThermoScientific Oxoid Antimicrobial Susceptibility Discs Recalled for Out-of-Specification Performance
Remel Inc. is recalling certain lots of ThermoScientific Oxoid Antimicrobial Susceptibility Discs because they were manufactured out of specification, potentially affecting laboratory test accuracy. The recall involves 327 units distributed nationwide and to Bermuda.
Product
ThermoScientific Oxoid Antimicrobial Susceptibility Discs Rx only Made in the United Kingdom
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2152-2021·2021-08-04
CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis misalignment
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106186) due to misaligned placement of the axis mark, which can cause blurred vision.
Product
CLARITI 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2153-2021·2021-08-04
Contact Lens Axis Mark Misalignment Causes Blurred Vision
CooperVision's FRESH DAY 1 DAY TORIC contact lenses (lot W0106186) are recalled because misaligned axis marks can cause blurred vision. Affected lenses were distributed worldwide, including in the US, France, Brazil, and other countries.
Product
FRESH DAY 1 DAY TORIC Power -07.00 -1.25/010 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V601000·2021-08-03
Fuel hose leak recall in 2021-2022 Kenworth and Peterbilt trucks
PACCAR is recalling 688 commercial trucks due to a fuel hose leak between the fuel pump and remote fuel filter head that increases fire risk. Free fuel hose replacement is being offered.
Product
KENWORTH — KENWORTH, PETERBILT T480, T280, T380, T370
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E070000·2021-08-03
Bendix Intellipark Electronic Control Unit Software Recall
Bendix is recalling Intellipark Dash Electronic Control Units that may fail to activate the parking brake, causing vehicles to move unintentionally.
Product
PARKING BRAKE:ELECTRICAL:CONTROL MODULE:SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V595000·2021-08-02
2021 Audi E-Tron: Unsecured glove box may interfere with air bag
Volkswagen is recalling certain 2021 Audi E-Tron vehicles because the right hinge pin for the glove box cover may not be properly secured, potentially interfering with knee air bag deployment in a crash.
Product
AUDI — AUDI E-TRON
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V597000·2021-08-02
Volvo Bus 9700 Recall: Wheelchair Lift Barrier May Fail Under Force
Volvo Bus is recalling 2009-2021 9700 vehicles with wheelchair lifts because the outer barrier may fail, increasing injury risk.
Product
VOLVO BUS — VOLVO BUS 9700
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V599000·2021-08-02
Software error may deactivate rear-view display in 2021 INFINITI Q60 vehicles
A software error may disable the rear-view camera display in 2021 INFINITI Q60 vehicles, reducing rear visibility and increasing crash risk. Nissan will update the software at no cost.
Product
INFINITI — INFINITI Q50, QX80, Q60
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V596000·2021-08-02
2022 Mitsubishi Outlander seat belt retractor defect affects child restraints
Mitsubishi is recalling certain 2022 Outlander vehicles due to seat belt retractors that may deactivate early, preventing child restraint systems from securing properly. Owners should contact MMNA at 1-888-648-7820 for free replacement.
Product
MITSUBISHI — MITSUBISHI OUTLANDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V598000·2021-08-02
2020 BMW X4 Engine Software Defect Disables Braking Assist
BMW is recalling multiple 2020-2021 models, including the X4, due to engine management software that may disable braking assist. Owners should contact BMW at 1-800-525-7417 for a free software update.
Product
BMW — BMW, TOYOTA 745LE, X4, X3, M340I
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V594000·2021-07-30
Kawasaki Recalls Ninja H2 SX Motorcycles Due to Rear Wheel Lockup Risk
Kawasaki is recalling 2018-2021 Ninja H2 SX motorcycles because insufficient grease in the rear hub needle-bearing may cause failure, leading to rear wheel lock-up and increased crash risk.
Product
KAWASAKI — KAWASAKI NINJA H2 SX, ZX1002A, ZX1002D
Category
Vehicle
Distribution
Distributed nationwide