State

US Virgin Islands product recalls

73,827 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

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.

56101–56125 of 74005

LowFDA (Devices)·Z-0550-2015·2014-12-17
Instrumed Recalls Gardner-Wells Traction Tongs for Regulatory Compliance
Instrumed International is withdrawing 190 Gardner-Wells traction tongs because the company did not market them before September 26, 1976, failing to meet FDA pre-amendment requirements.
Product
Gardner-Wells traction tongs are skull tongs for traction used to immobilize a patient with a cervical spine injury (e.g., fracture or dislocation) and sold under the Millenium Surgical, Echo Instruments, Adler Instrument, Surgical Direct, Stealth Surgical, CareFusion, and Boss…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0534-2015·2014-12-17
Instrumed Recalls Zipser Meatus Clamps Due to Regulatory Non-Compliance
Instrumed International is withdrawing 81 Zipser Meatus Clamps because the company did not market the devices prior to 1976, failing to meet FDA requirements for pre-amendment devices.
Product
A zipser clamp is an instrument used to compress reduce blood flow to the penis and reduce pain and is sold under the Medline Industries, Boss Instruments, Millennium Surgical, Medetz Surgical, Surgical Direct, and Surgipro brand names.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0548-2015·2014-12-17
Instrumed Recalls Hudson Cranial Drill Sets for Regulatory Non-Compliance
Instrumed International is withdrawing five Hudson cranial drill sets because the company failed to meet FDA requirements for marketing pre-amendment devices.
Product
Hudson cranial drill sets (w/ brace and 5 attachments) are bone cutting and drilling instruments that are used without a power source on a patient's skull and sold under the Symmetry Surgical, Medfix International, Stealth Surgical, and Boss Instruments brand names.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V795000·2014-12-16
Chrysler Recalls 2006-2007 Dodge and Mitsubishi Trucks for Ignition Switch Defect
Chrysler is recalling 54,164 vehicles because broken springs in the clutch ignition interlock switch can cause unintended movement or no-start conditions.
Product
DODGE — DODGE, MITSUBISHI RAM 2500, DAKOTA, RAM 3500, RAIDER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V796000·2014-12-16
Chrysler Recalls 2005 Dodge Ram 1500 Trucks for Rear Axle Defect
Chrysler is recalling 2005 Dodge Ram 1500 trucks because a rear axle pinion nut may loosen, potentially causing loss of vehicle control.
Product
DODGE — DODGE RAM 1500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V794000·2014-12-16
Harley-Davidson Recalls 2012 Dyna and Softail Motorcycles for Brake Master Cylinder Defect
Harley-Davidson is recalling 19,015 model year 2012 Dyna and Softail motorcycles because corrosion in the front brake master cylinder could cause a loss of front brakes and increase crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON SOFTAIL, DYNA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V793000·2014-12-16
Terex Advance Recalls 2013-2015 Concrete Mixer Trucks for Suspension Defect
Terex Advance is recalling 2013-2015 Front Discharge Concrete Mixer Trucks because improperly secured nuts may cause the front axle leaf spring to partially disconnect, increasing crash risk.
Product
TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V792000·2014-12-16
Honda Recalls Acura RLX Vehicles for Headlight Film Defect
Honda is recalling specific 2014-2015 Acura RLX and RLX Hybrid vehicles because headlight film may delaminate, reducing light output and increasing crash risk.
Product
ACURA — ACURA RLX, RLX HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15047·2014-12-16
WindowTex Recalls Custom Roller Shades Due to Falling Hazard
WindowTex is recalling about 6,800 custom roller shades because a steel pin can dislodge, causing the shade to fall and pose an injury risk.
Product
Roller Window Shades
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V791000·2014-12-15
Hino Recalls 2005-2015 Trucks Due to Parking Brake Wear
Hino is recalling 2005-2015 NE8J, NF8J, and ND8J trucks because parking brake components may wear, causing the brake to release or fail to engage, increasing crash risk.
Product
HINO — HINO NE8J, NF8J, ND8J
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V788000·2014-12-15
Honda Recalls 2015 Crosstour Vehicles for Side Air Bag Defect
Honda is recalling 2015 Crosstour vehicles because the side curtain air bag inflator tube may be incorrectly manufactured, potentially affecting air bag performance in a crash.
Product
HONDA — HONDA CROSSTOUR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V790000·2014-12-15
Volkswagen Recalls 2015 Jetta Vehicles for Headlight Software Defect
Volkswagen is recalling 2015 Jetta vehicles because a software error may cause low beam headlights to turn off when high beams are activated, reducing visibility.
Product
VOLKSWAGEN — VOLKSWAGEN JETTA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V789000·2014-12-15
MINI Cooper Recall for Transmission Software Rollaway Risk
BMW is recalling 2014-2015 MINI Cooper vehicles because incorrect transmission software may allow the car to roll away if the driver exits without engaging Park.
Product
MINI — MINI COOPER S, COOPER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V787000·2014-12-12
Ford Recalls 2005-2006 GT Vehicles for Air Bag Inflator Defect
Ford is recalling 2005-2006 GT vehicles sold in high-humidity areas because the passenger air bag inflator may rupture during deployment, potentially causing serious injury.
Product
FORD — FORD GT
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15045·2014-12-12
UVEX Recalls Bicycle Helmets Due to Chinstrap Anchor Failure Risk
UVEX Sports is recalling 46,800 bicycle helmets because the chinstrap anchor can fail, causing the helmet to slide off and posing a head injury hazard.
Product
UVEX Bicycle Helmets
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0458-2015·2014-12-10
ConMed Adult Radiotransparent Electrode Recall Due to Connection Failure Risk
ConMed is recalling Adult Radiotransparent Electrodes because design changes to Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.
Product
ADULT Radiotransparent Electrode, REF/Catalog Number 2516H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0462-2015·2014-12-10
ConMed Multifunction Electrodes Recalled for Connection Design Failure
ConMed is recalling multifunction electrodes due to a design change that may prevent connection to Philips AEDs, potentially delaying therapy.
Product
CONMED ADULT R2 Multifunction Electrodes, REF/Catalog Number 3115-1751, Direct Connect to Philips Heartstart, Rx ONLY --- ASSEMBLED IN MEXICO -Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use, disposable…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0460-2015·2014-12-10
ConMed Pediatric Electrodes Recalled Due to Connection Design Changes
ConMed is recalling 174,610 pediatric electrodes because design changes to Philips AEDs may prevent connection, delaying therapy and risking death or serious injury.
Product
MINI PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2602H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR--Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0456-2015·2014-12-10
ConMed Adult Radiotransparent Electrodes Recalled for Connection Design Changes
ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
Product
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0457-2015·2014-12-10
ConMed Adult Radiotransparent Electrode Recall Due to Connection Design Changes
ConMed is recalling 174,610 Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
Product
ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0455-2015·2014-12-10
ConMed Adult Radiotransparent Electrode Recall Due to Connection Design Changes
ConMed is recalling Adult Radiotransparent Electrodes because design changes to Philips AED connections may cause connection failures, potentially delaying therapy and resulting in patient death or serious injury.
Product
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0461-2015·2014-12-10
ConMed Pediatric Multifunction Electrodes Recalled for Connection Design Flaws
ConMed is recalling Pediatric R2 Multifunction Electrodes because design changes to the connection with Philips Heartstart devices may cause connection failures, potentially delaying therapy and leading to patient death or serious injury.
Product
CONMED PEDIATRIC R2 Multifunction Electrodes, REF/Catalog Number 3115-1750, Direct Connect to Philips Heartstart, Rx ONLY --- ASSEMBLED IN MEXICO -Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use…
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0459-2015·2014-12-10
ConMed Pediatric Radiotransparent Electrode Recall Due to Connection Design Changes
ConMed is recalling 174,610 pediatric radiotransparent electrodes because design changes to Philips AED connections may cause therapy delays, risking patient death or serious injury.
Product
PEDIATRIC Radiotransparent Electrode, REF/Catalog Number 2603H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0454-2015·2014-12-10
ConMed Adult Radiotransparent Electrodes Recalled for Connection Design Failure
ConMed is recalling Adult Radiotransparent Electrodes because a design change in Philips AEDs may prevent connection, delaying therapy and risking patient death or serious injury.
Product
ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring applications. This product is a single-use…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0612-2015·2014-12-10
Chetak New York Recalls Deep Raw Cashew Pieces Due to Salmonella Risk
Chetak New York LLC is recalling Deep Raw Cashew Pieces because they may be contaminated with Salmonella. The recall covers 11,320 packages distributed nationwide.
Product
Deep Raw Cashew Pieces Distributed by Chetak New York LLC Edison, NJ 08837 USA 7 oz. - UPC 011433133104 - 20 per case 14 oz. - UPC 011433133111 - 20 per case 28 oz. - UPC 011433133128 - 10 per case packaged in a plastic bag; for dry storage
Category
Food
Distribution
Distributed nationwide