State

US Virgin Islands product recalls

73,198 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: 30
Most recent: 2026-09-23

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 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15201–15225 of 73375

ModerateFDA (Devices)·Z-2095-2023·2023-07-12
Teleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions
TELEFLEX LLC recalled the Pilling O'REILLY ESOPHAGEAL RETRACTOR (REF 381801A) due to incomplete pre-cleaning instructions in the product's Instructions for Use. The recall affects 365 units distributed nationwide and internationally.
Product
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2084-2023·2023-07-12
Collagen matrix recalled for endotoxin testing methodology issues
TEI Biosciences recalled 665 units of Revize-X collagen matrix nationwide due to possible out-of-specification endotoxin test results caused by issues with the company's testing procedures. No illnesses have been reported.
Product
Revize-X; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 12x6 cm and 10x9 cm.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0892-2023·2023-07-12
Prescription Drug Tizanidine Tablets Recalled for Failed Dissolution Specifications
Amerisource Health Services LLC recalls approximately 4,971 cartons of Tizanidine Tablets due to failed dissolution specifications. Tablets that do not dissolve properly may not provide intended therapeutic benefit.
Product
TIZANIDINE — TIZANIDINE (TIZANIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2096-2023·2023-07-12
Teleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions
Teleflex LLC is recalling 170 units of the Pilling Lowsley Prostatic Retractor due to incomplete pre-cleaning instructions in the user manual. Incomplete instructions may prevent proper sterilization of the surgical instrument.
Product
Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2093-2023·2023-07-12
COVID-19 Test Strips Recalled for Lot Number Label Discrepancy
NeuMoDx SARS-CoV-2 test strips from lot 123909 have conflicting lot numbers between the package label and barcode label that the instrument reads.
Product
NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP).…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V474000·2023-07-11
Prevost H3-45 Turn Signal Light Failure Increases Crash Risk
Prevost is recalling 2022-2024 H3-45 and H3-45 VIP vehicles because the right front turn signal light may fail when activated. Inoperative turn signals and hazard lights reduce visibility to other drivers and increase crash risk.
Product
PREVOST — PREVOST H3-45 VIP, H3-45
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V475000·2023-07-11
Prevost Recalls X3-45 Commuter Buses Due to Seat Bolt Loosening
Prevost is recalling 2021 and 2023 X3-45 Commuter buses because a seat bolt may loosen, leaving the seat back unsecured and increasing crash injury risk.
Product
PREVOST — PREVOST X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V485000·2023-07-11
2023 Toyota RAV4 Recalled for Improperly Installed Tire Valve Stems
Gulf States Toyota is recalling 195 2023 Toyota RAV4 vehicles equipped with 17" black alloy wheels. The tire valve stems may be improperly installed or damaged, potentially causing air leakage, underinflation, and crash risk.
Product
TOYOTA — TOYOTA RAV4
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E053000·2023-07-11
Seats Incorporated Recalls Passenger Flip Seats Due to Missing Safety Clip
Seats Incorporated is recalling specific passenger flip-up seats that may be missing a safety clip, which could allow the seat to fall and cause injury.
Product
SEATS:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V472000·2023-07-10
Yamaha Recalls 2022 Tenere 700 Motorcycles Due to Brake Caliper Bolt Defect
Yamaha is recalling 2022 Tenere 700 motorcycles because front brake caliper bolts may have incorrect thread lengths, risking brake failure.
Product
YAMAHA — YAMAHA TENERE 700
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V473000·2023-07-10
Boreas Camper XT Travel Trailers Recalled for Gas Leak Risk
Boreas Campers is recalling 2021-2022 XT travel trailers because a cooktop component may fracture and cause a gas leak, increasing fire risk.
Product
BOREAS CAMPER — BOREAS CAMPER XT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V471000·2023-07-10
2023 BMW XM and 2024 X5-X7 vehicles recalled for knee air bag defect
BMW of North America is recalling 2023 XM and certain 2024 X5, X6, and X7 vehicles because the knee air bag may not have been manufactured correctly and could fail to deploy during a crash. Dealers will replace the air bag free of charge.
Product
BMW — BMW X5, X6, XM, X7
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E052000·2023-07-10
Dana Spicer Driveshafts Recalled for Risk of Breaking Under Load
Dana Incorporated is recalling specific Dana-Spicer driveshafts that can break under certain loading conditions, potentially causing a loss of drive power and increasing crash risk.
Product
POWER TRAIN:DRIVELINE:DRIVESHAFT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23E051000·2023-07-07
Ironman 4x4 Recalls Pro Forge Upper Control Arms for Steering Loss Risk
Ironman 4x4 is recalling Pro Forge upper control arms because the ball joint may fail, causing loss of steering control.
Product
SUSPENSION:FRONT:CONTROL ARM:UPPER BALL JOINT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V468000·2023-07-07
2023 Toyota Tundra Spare Tire Carrier May Detach Due to Insufficient Welds
Toyota is recalling certain 2023 Tundra, Tundra Hybrid, and Sequoia Hybrid vehicles due to insufficiently welded spare tire carrier assemblies that may break and allow the spare tire to detach, increasing crash risk.
Product
TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA, SEQUOIA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V469000·2023-07-07
Newmar motorhomes recalled for defective seat belt mounting brackets
Newmar is recalling certain 2019–2023 motorhomes because modified seat belt mounting brackets can fail to properly restrain occupants in a crash, violating federal safety standards.
Product
NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT, SUPER STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V467000·2023-07-06
Freightliner Recalls eCascadia Trucks for E-Axle Welding Defect
Daimler Trucks is recalling 2023-2024 Freightliner eCascadia vehicles because a defective e-axle weld may cause sudden loss of drive power, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER E-CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·23238·2023-07-06
VRURC Portable Chargers Recalled Due to Fire Hazard
VRURC portable chargers (model OD-B7) sold on Amazon.com from July 2021 through May 2023 can ignite and pose a fire hazard. One charger caught fire on a commercial flight, injuring four flight attendants.
Product
VRURC portable chargers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23239·2023-07-06
woom ORIGINAL Kids' Bicycles Recalled Due to Fall Hazard
woom Bikes USA recalls about 84,000 woom ORIGINAL children's bicycles from model years 2018–2021. The stem and handlebar can detach, causing riders to lose control and fall.
Product
woom ORIGINAL Bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23772·2023-07-06
Yamaha Model Year 2023 Golf Cars and PTVs Recalled for Crash and Death Hazards
Yamaha is recalling about 11,000 Model Year 2023 Golf Cars, Personal Transportation Vehicles, and Umax models because the accelerator spring can become dislodged, preventing the accelerator pedal from returning to rest and posing crash, injury, and death hazards.
Product
Model Year 2023 Yamaha Golf Car, Personal Transportation Vehicles (PTV) and Umax
Category
Vehicle
Distribution
Distributed nationwide
ModerateCPSC·23240·2023-07-06
Husqvarna 300 Series Snow Blowers Recalled for Unexpected Drive Engagement
Husqvarna is recalling about 2,700 Residential 300 Series Snow Blowers because the auger pulley bolt can loosen, causing the drive to unexpectedly engage and potentially collide with users. No injuries have been reported.
Product
Residential 300 Series Snow Blowers
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1876-2023·2023-07-05
Endotracheal Tube Connector Disconnection Recall — FDA Class I
TELEFLEX endotracheal tubes (Murphy design) may have a disconnected 15mm connector. Approximately 12,382 affected units were distributed nationwide. Healthcare facilities should inspect tubes before use.
Product
Endotracheal Tube oral/nasal uncuffed/plain - Murphy, REF 100382050
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1893-2023·2023-07-05
Teleflex Endotracheal Tubes Recalled Due to Connector Disconnection Risk
Teleflex is recalling 18,620 endotracheal tubes due to reported disconnection of 15mm connectors. The tubes are used for oral and nasal intubation and were distributed nationwide.
Product
Endotracheal Tube oral/nasal Murphy Eye, High Volume, Low Pressure Cuff, REF 112082095
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2000-2023·2023-07-05
MEGADYNE MEGA SOFT Return Electrode Recalled for Burns During Surgical Procedures
Megadyne Medical Products is recalling the MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode due to reported patient burns that occurred during electrosurgical procedures.
Product
MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1994-2023·2023-07-05
MEGADYNE MEGA 2000 Patient Return Electrode Recalled Due to Patient Burns
The FDA is recalling 21,100 units of the MEGADYNE MEGA 2000 Patient Return Electrode due to reports of patient burns during electrosurgical procedures. All units distributed nationwide are affected.
Product
MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery
Category
Medical Device
Distribution
Distributed nationwide