State

US Virgin Islands product recalls

73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28901–28925 of 73774

SevereUSDA FSIS·007-2020-EXP ·2020-05-22
Conagra Recalls Frozen Chicken and Turkey Bowls Due to Rock Contamination
Conagra Brands is recalling approximately 276,872 pounds of frozen Healthy Choice Power Bowls because they may contain small rocks. No illnesses have been reported.
Product
Conagra Brands (Conagra Foods Packaged Foods, LLC) — Conagra Brands, Inc. Recalls Frozen Not-Ready-To-Eat Chicken and Turkey Bowl Products due to Possible Foreign Matter Contamination
Category
Food
Distribution
Distributed nationwide
HighNHTSA·20V298000·2020-05-22
Mercedes-Benz Recalls 2012 C-Class Vehicles for Incorrect Air Bag Replacement
Mercedes-Benz is recalling 2012 C-Class vehicles where an incorrect front passenger air bag may have been installed during a prior recall, potentially reducing crash protection.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG C63, C250, C300, C350
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V297000·2020-05-22
2020-2021 Forest River Surveyor Travel Trailers Safety Chain Recall
Forest River is recalling 2020-2021 Surveyor travel trailers because the safety chains are insufficient for the trailer's weight rating and may break if the trailer becomes unhitched, risking complete detachment.
Product
FOREST RIVER — FOREST RIVER SURVEYOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V299000·2020-05-22
Triple E Recalls 2020 Unity Travel Trailers Due to Latch Defect
Triple E is recalling 2020 Unity travel trailers because a latch may lock, blocking access to the propane shutoff valve and increasing fire risk.
Product
TRIPLE E — TRIPLE E UNITY
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V296000·2020-05-22
KZRV Recalls 2018 Escape Trailers Due to Incorrect Tire Labels
KZRV is recalling 2018 Escape recreational trailers because incorrect tire labels may cause overinflation, increasing crash risk.
Product
KZRV — KZRV ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V294000·2020-05-21
Dennis Eagle Elite Garbage Trucks Recalled for Braking System Defect
Dennis Eagle is recalling 2017-2018 Elite garbage trucks because the anti-lock braking system may activate on the wrong side, increasing stopping distance.
Product
DENNIS EAGLE — DENNIS EAGLE ELITE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V295000·2020-05-21
2021 Chevrolet Trailblazer lacks tire size and pressure label information
General Motors is recalling certain 2021 Chevrolet Trailblazer vehicles with optional sport terrain tires because their certification labels do not show tire size and cold tire pressure information required by federal safety standards.
Product
CHEVROLET — CHEVROLET TRAILBLAZER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·20746·2020-05-21
Viva Doria Recalls Wintergreen Essential Oil Due to Packaging Defect
Viva Doria is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Product
Viva Doria Wintergreen Essential Oil
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·20747·2020-05-21
Herman Miller and Design Within Reach Recall Dressers and Cabinets for Tip-Over Hazards
Herman Miller and Design Within Reach are recalling Nelson and Lauki dressers and cabinets because they can tip over and entrap children. Consumers should stop using unanchored units and contact the company for a refund.
Product
Nelson and Lauki Dressers and Cabinets
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·20V286000·2020-05-20
Toyota Recalls 2019-2020 RAV4 Models for Front Suspension Arm Cracks
Toyota is recalling 2019-2020 RAV4 and RAV4 Hybrid vehicles because front lower suspension arms may crack and separate, risking loss of vehicle control.
Product
TOYOTA — TOYOTA RAV4, RAV4 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1932-2020·2020-05-20
Philips Zenition 50 Medical Device Recalled for Electrical Contact Failure
Philips is recalling 25 Zenition 50 devices because strain relief loss can cause electrical contacts to break, potentially exposing live parts or losing the video signal.
Product
Philips Zenition 50, System code 718096 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V293000·2020-05-20
Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect
Vac-Tron is recalling 2016-2020 vacuum excavator trailers because the rear extends too far, failing federal safety standards and increasing crash risks.
Product
VAC-TRON — VAC-TRON CS 1270 GT, CS 870 GT, CS 873 GT, CV 1273 GT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1945-2020·2020-05-20
Beckman Coulter iQ200 Urine Analyzer Recalled for Electrical Short Risk
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers due to a defect in the SATA power adapter cable that poses a risk of electrical short, charring, smoke, or flames.
Product
iQ200 Series Urine Microscopy Analyzer- All part numbers
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1944-2020·2020-05-20
Beckman Coulter iChem VELOCITY Urine Chemistry System Recalled for Fire Risk
Beckman Coulter is recalling iChem VELOCITY Urine Chemistry Systems due to a defect in the SATA power adapter cable that poses a risk of electrical short, smoke, or flames.
Product
iChem¿VELOCITY Urine Chemistry System-
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V284000·2020-05-20
REV Recalls 2018-2020 Type 1 Ambulances for Rear Brake Line Wear
REV is recalling 2018-2020 Type 1 ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.
Product
FRONTLINE — FRONTLINE, ROAD RESCUE, WHEELED COACH TYPE I
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V291000·2020-05-20
Horton Emergency Vehicles Recalled for Rear Brake Line Wear Risk
Halcore is recalling 2018-2020 Horton ambulances because a rear brake line may wear from contact with suspension parts, risking brake loss.
Product
HORTON — HORTON TYPE III, TYPE I
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1957-2020·2020-05-20
Siemens Cios Alpha Mobile X-Ray System Recalled for Electrical Shock Risk
Siemens is recalling four Cios Alpha mobile X-ray systems because unplugging the main cable during a clinical session can expose users to unsafe electrical voltage.
Product
Siemens Cios Alpha VA20-mobile X-Ray system Material # 10308191 The Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1933-2020·2020-05-20
Philips Zenition 70 Trolley Cable Recall for Electrical Contact Failure
Philips is recalling 25 Zenition 70 systems because strain relief loss on the trolley cable can break electrical contacts, exposing live parts.
Product
Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guidance and visualization during diagnostic, interventional and surgical procedures on all patients, except neonates (birth to one month), within the limits of the device.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1991-2020·2020-05-20
FDA Recalls Dover Foley Catheters Due to Temperature Sensor Inaccuracy
The FDA is recalling specific lots of Dover Foley catheters because their temperature sensors may not measure accurately. This could lead to incorrect patient diagnoses.
Product
Dover 100% Silicone Silver-Hydrogel Coated Premium Urine Meter Foley Tray 400mL, Premium, Urine Meter, 16 Fr/Ch (5.3 mm), 5 mL Catheter Pre-connected to 2000 mL Drainage Bag with Luer-Lock Sampling, Temperature Sensor and Adhesive Catheter Securement, Sterile, Product Code…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1269-2020·2020-05-20
MasterPharm Recalls Finasteride Plus Capsules Due to Minoxidil Contamination
MasterPharm LLC is recalling Finasteride Plus 1.25 mg capsules because they were found to contain minoxidil. The recall covers 7,260 capsules distributed nationwide.
Product
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V283000·2020-05-20
BMW and MINI Recall Vehicles Due to Rollover Sensor Defect
BMW is recalling certain 2020-2021 vehicles because a rollover sensor defect may prevent air bags and seat belt pretensioners from deploying in a crash.
Product
MINI — MINI, BMW COOPER S CLUBMAN, X1, X2, COOPER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V292000·2020-05-20
Vac-Tron Vacuum Excavator Trailers Recalled for Rear Impact Protection Defect
Vac-Tron is recalling 2016-2020 vacuum excavator trailers because the rear extends too far, reducing impact protection and increasing crash risk.
Product
VAC-TRON — VAC-TRON CS 1273 GT, CS 800 GT, CS 1270 SGT, CS 1270 GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1974-2020·2020-05-20
Access Scientific Recalls Saline Flush Syringes Due to Packaging Holes
Access Scientific LLC is recalling 7,395 saline flush syringes used in POWERWAND kits because holes in the packaging compromised sterility.
Product
BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 8cm Quick Kit. REF/UDI / 94104/10859821006169 - Product Usage: is used to gain access to the vascular system to sample blood and administer fluids intravenously. It may be used for power injection of contrast…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2004-2020·2020-05-20
Inpeco Abbott Accelerator a3600 Interface Module Recalled for Cross-Contamination Risk
Inpeco S.A. is recalling 273 Abbott Accelerator a3600 Interface Modules because a timeout error could cause sample cross-contamination.
Product
Abbott Accelerator a3600, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: ACP-208-00 - Product Usage: The FlexLab (aka Accelerator a3600) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1929-2020·2020-05-20
Encore Medical Recalls EMPOWR Acetabular Impactor Balls Due to Fracturing
Encore Medical is recalling 86 units of EMPOWR Acetabular Impactor Balls because they may fracture during use, potentially leaving debris in the joint space.
Product
EMPOWR Acetabular System, Non-Sterile, Model Numbers 803-15-023 803-15-026 803-15-027 803-15-028 803-15-029 803-15-030 Product Usage: The EMPOWR Acetabular Impactor Balls is intended for use in joint replacement in patients suffering from disability due to…
Category
Medical Device
Distribution
Distributed nationwide