The Recall Desk

State

US Virgin Islands product recalls

73,509 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.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25426–25450 of 73686

  • ModerateUSDA FSIS·pha-04022021-01·2021-04-02

    USDA Issues Public Health Alert for Raw Ground Chorizo Sausage

    USDA FSIS issued a public health alert for raw ground chorizo sausage due to possible contamination with hard crystalline material. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for Raw Ground Chorizo Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2021·2021-04-01

    Rong Shing Trading Recalls Ineligible Chinese Beef Hot Pot Base

    Rong Shing Trading Inc. is recalling approximately 3,365 pounds of Chinese-style hot pot base containing beef tallow imported from China, a country ineligible to export beef to the U.S.

    Product
    Rong Shing Trading Inc. Recalls Ineligible Beef Products Imported from China
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V229000·2021-04-01

    Mercedes-Benz Recalls Vehicles for Steering Shaft Bearing Separation Risk

    Mercedes-Benz is recalling specific 2017-2018 models because a steering shaft defect could cause loss of control. Dealers will inspect and replace the shaft free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250, CLA250, AMG CLA45, AMG GLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21735·2021-04-01

    BATTOP Foldable Infant Bath Seats Recalled for Drowning Hazard

    BATTOP is recalling about 5,000 foldable infant bath seats sold on Amazon.com because they can tip over, posing a drowning risk to babies.

    Product
    Foldable Infant Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21734·2021-04-01

    doTERRA Recalls Essential Oils Due to Non-Child-Resistant Packaging

    doTERRA is recalling 1.3 million bottles of Deep Blue, PastTense, and Deep Blue Touch essential oils because the packaging is not child-resistant, posing a poisoning risk.

    Product
    doTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V233000·2021-04-01

    Mack heavy trucks recalled for electronic stability control software malfunction

    Mack trucks (2018-2022) with electronic stability control may drift out of their lane at certain speeds, increasing crash risk. Dealers will reprogram the control units free of charge.

    Product
    MACK — MACK GRANITE (GR), GRANITE (GU), PINNACLE (CXU), PINNACLE (CHU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V230000·2021-04-01

    2021 Mercedes-Benz Vehicles Recalled for Faulty Seat Switch

    2021 Mercedes-Benz vehicles are being recalled due to a faulty seat position switch that may prevent airbags and seatbelt force limiters from activating during a crash. MBUSA will replace the switches free of charge.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, C 300, E 350, AMG GT63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V231000·2021-04-01

    2021 Mercedes-Benz GLB vehicles recalled for potentially detaching tailgate spoilers

    Mercedes-Benz is recalling certain 2021 GLB35 AMG and 2020–2021 GLB250 vehicles because the side spoilers on the tailgate might not have been installed correctly, allowing them to detach and create a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250, AMG GLB35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V226000·2021-04-01

    2021 International RH and LT Vehicles Parking Brake Defect

    Certain 2021 International RH and LT vehicles have a defective spring brake chamber that may allow the parking brake to malfunction, increasing crash risk. Navistar will replace the defective brake chambers at no cost.

    Product
    INTERNATIONAL — INTERNATIONAL RH, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V228000·2021-04-01

    Mercedes-Benz Recalls 2021 E-Class Models for Parking Sensor Defect

    Mercedes-Benz is recalling 2021 E350, E450, and AMG E63 vehicles because the parking control unit may fail to display the rearview camera or detect objects, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, E 450, AMG E63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V227000·2021-04-01

    2021 International Trucks Recalled for Air Brake Check Valve Manufacturing Defect

    Navistar recalls 2021 International trucks for defective air brake check valves that may cause unintended brake application and increase crash risk. The SC-3 valve's retainer is not properly seated.

    Product
    INTERNATIONAL — INTERNATIONAL RH, LT, HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0311-2021·2021-03-31

    Adam's Secret Extra Strength 3000 Recalled for Unapproved Ingredients

    The FDA is recalling Adam's Secret Extra Strength 3000 because it contains unapproved drugs tadalafil and sildenafil.

    Product
    Adam's Secret Extra Strength 3000, 840 mg, 10 count blister packs, Distributed by AS Inc., Made in USA, UPC 6 09728 43452 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0310-2021·2021-03-31

    Adam's Secret Extra Strength Recalled for Unapproved Active Ingredients

    Adam's Secret Extra Strength 1500 is being recalled because FDA analysis found unapproved drugs tadalafil and sildenafil in the product.

    Product
    Adam's Secret Extra Strength 1500, 800 mg, 10 count blister packs, Distributed by KP Inc., Made in USA, UPC 6 09728 43462 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1284-2021·2021-03-31

    Caire Diagnostics Recalls FenomPro Devices Due to Erroneous High FeNO Readings

    Caire Diagnostics is recalling FenomPro devices because calibration drift and software errors may cause erroneously high FeNO readings, potentially leading to premature discontinuation of asthma treatment.

    Product
    CAIRE DIAGNOSTICS FenomPro REF 900-0001 SN ***** - Product Usage: a portable, non-invasive device to measure fractional exhaled nitric oxide (FeNO) in human breath. Fenom Pro should not be used in critical care, emergency care or in anesthesiology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1280-2021·2021-03-31

    Baxter Recalls Prismaflex Preventative Maintenance Kits Due to Tubing Performance Variability

    Baxter Healthcare is recalling Prismaflex Preventative Maintenance Kits and spare part kits because tubing performance variability may cause alarms during or after system self-tests.

    Product
    Preventative Maintenance Kits G5010007) and spare part kits (G5064801 and G5006203) - Product Usage: For Prismaflex Control Units, used for Continuous Renal Replacement Therapy (CRRT).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1282-2021·2021-03-31

    Hitachi Arietta 850 Ultrasound System Recalled for Acoustic Output Error

    Hitachi Medical Systems America Inc. is recalling Arietta 850 ultrasound systems with specific software versions due to an error that can cause acoustic output to exceed regulatory limits.

    Product
    Ultrasonic pulsed doppler imaging system - Product Usage: intended for use by trained personnel (doctor, Sonographer, etc.) for the diagnostic ultrasound evaluation of Fetal, Abdominal, Intra-operative (Spec.), Intraoperative (Neuro.), Laparoscopic, Pediatric, Small Organ…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V225000·2021-03-31

    Harley-Davidson motorcycles recalled for faulty headlight bulbs and visibility loss

    Harley-Davidson is recalling 2019-2021 Sportster motorcycles and replacement headlight assemblies because the glass bulb may fail, causing loss of both high and low beams and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL1200NS, XL1200C, XL883N, XL883L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V224000·2021-03-31

    2021 Porsche Macan recalled for loose shock absorber screw connections

    Certain 2021 Porsche Macan models have improperly tightened screw connections on shock absorbers, which could compromise braking and vehicle control. Porsche will repair the connections free of charge.

    Product
    PORSCHE — PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1297-2021·2021-03-31

    Stryker S-Series Equipment Management System Recall for Brake Disengagement Risk

    Stryker is recalling S-Series Equipment Management Systems because capacitive touch controls may disengage when electrocautery devices are in use.

    Product
    S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected within the S-Series Finished Good Model Number o P38198 - ASM, MFR CONTROLLER, FIXED STANDARD o P38199 - ASM, MFR CONTROLLER, LIFT STANDARD o P40553 - ASM, MFR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2021·2021-03-31

    Olympus Recalls TJF-Q190V Duodenoscopes Due to Reported Mucosal Injury

    Olympus is recalling 1,564 TJF-Q190V duodenoscopes and accessories worldwide due to complaints of mucosal injury associated with the forceps elevator region.

    Product
    Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source, documentation equipment, monitor, Endo Therapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2021·2021-03-31

    RayCare 3B Oncology Software Recalled for Data Loss During Upgrade

    RaySearch Laboratories AB is recalling RayCare 3B software because patient messages may be lost when upgrading from RayCare 2.

    Product
    RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information system that supports healthcare professionals in delivering cancer care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1294-2021·2021-03-31

    Teleflex Recalls Rusch Polaris Laryngoscopes Due to Handle Cracking

    Teleflex is voluntarily recalling Rusch Polaris laryngoscopes because customers reported that the handles develop cracks or break at the hinge.

    Product
    RUSCH¿ POLARIS" Laryngoscope - Product Usage: intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2021·2021-03-31

    Teleflex Recalls PLEUR-EVAC Thoracic Catheters Due to Sterility Concerns

    Teleflex is recalling 520 PLEUR-EVAC Thoracic Catheters because the company cannot guarantee the devices are sterile.

    Product
    PLEUR-EVAC Thoracic Catheters (CATHETER, IRRIGATION). The thoracic catheter is a sterile, non pyrogenic, single use device that allows drainage from the mediastinum and/or the pleural space. The thoracic catheter is composed of Phthalate-free PVC material and is available in…
    Category
    Medical Device
    Distribution
    Distributed nationwide