The Recall Desk

State

US Virgin Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32776–32800 of 73900

  • LowFDA (Devices)·Z-2139-2019·2019-08-14

    Sage Products Recalls Independent Care System Due to Damaged Mouthpaste Tubes

    Sage Products Inc is voluntarily recalling a lot of Independent Care System kits because the included Sodium Bicarbonate Mouthpaste tubes may be cosmetically damaged.

    Product
    Toothete Oral Care Sodium Bicarbonate Mouthpaste, Net Wt. 1/3 oz/ 9g, included in Independent Care System. The system is an oral care convenience kit which includes: an Ultra-Soft Toothbrush, 0.5 oz. tube of Mouth Moisturizer, 0.33 oz. /9g tube of Sodium Bicarbonate Mouthpaste…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·19767·2019-08-13

    SunSetter Recalls Vinyl Covers for Motorized Awnings Due to Fall Hazards

    SunSetter is recalling vinyl covers for motorized awnings because they can cause unexpected opening and falls. One death and six injuries have been reported.

    Product
    Vinyl covers for SunSetter Motorized Awnings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V592000·2019-08-13

    E-One Recalls 2019 Fire Trucks Due to Air Bag Defect

    E-One is recalling 2019 Cyclone II and Typhoon fire trucks because air bag cushions may detach and fail to inflate during a crash.

    Product
    E-ONE — E-ONE TYPHOON, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V587000·2019-08-12

    Mercedes-Benz Recalls 2020 GLE and GLS Models for Fire Risk

    Mercedes-Benz is recalling 2020 GLE and GLS vehicles because incorrectly installed air conditioner drain hoses may cause water to enter the cabin, increasing the risk of fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, GLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V590000·2019-08-12

    Ford Recalls 2015 Fusion and Lincoln MKZ for Seat Belt Cable Defect

    Ford is recalling 2015 Fusion and Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in crashes.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V585000·2019-08-12

    Mercedes-Benz Recalls GLA 250 Models for Loose Rear Seatbelt Anchor

    Mercedes-Benz is recalling 2018-2019 GLA 250 vehicles because the rear middle seatbelt anchor may be loose, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V591000·2019-08-12

    NHTSA Recalls 2019 Mercedes-Benz and Freightliner Sprinter Vehicles for Taillight Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because taillights may dim or turn off if the turn switch is moved quickly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V589000·2019-08-12

    BMW Recalls 2020 745e xDrive for Seat Belt Warning Software Error

    BMW is recalling 2020 745e xDrive vehicles because a software error may disable the audible seat belt warning for the driver, increasing injury risk in a crash.

    Product
    BMW — BMW 745E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V586000·2019-08-09

    Mercedes-Benz Recalls C300 and C43 Models for Battery Bracket Defect

    Mercedes-Benz is recalling 2018-2019 C300 and C43 AMG vehicles because the 12-volt battery bracket may be unsecured, risking terminal disconnection in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, AMG C43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V584000·2019-08-09

    Mercedes-Benz Recalls 2019 S 450 for Air Bag Deployment Risk

    Mercedes-Benz is recalling one 2019 S 450 vehicle because improperly installed pillar covers may prevent side curtain air bags from deploying correctly during a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V582000·2019-08-09

    Dennis Eagle Recalls 2017 Diego Vehicles for Electrical System Defect

    Dennis Eagle is recalling one 2017 Diego vehicle because a switch failure may cause instrument controls to move sides and disable the electronic braking system.

    Product
    DENNIS EAGLE — DENNIS EAGLE DIEGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V581000·2019-08-08

    Navistar Recalls 2019-2020 IC Buses Due to Roof Hatch Handle Defect

    Navistar is recalling 2019-2020 IC RE and IC CE commercial buses because the roof hatch external handle may break, potentially preventing emergency egress.

    Product
    IC BUS — IC BUS RECB, CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1579-2019·2019-08-07

    ImprimisRx Recalls Subpotent Timolol-Dorzolamide-Latanoprost Ophthalmic Drops

    ImprimisRx NJ is recalling 246 bottles of Timolol-Dorzolamide-Latanoprost ophthalmic drops because the medication was found to be subpotent.

    Product
    Timolol- Dorzolamide- Latanoprost P-F (0.5/2.0/0.005%) ophthalmic drops, packaged in 5mL bottles, Rx only, ImprimisRx NJ 1705 Route 46 West, Suite 4, Ledgewood, NJ 07852 (844) 446-6979
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2088-2019·2019-08-07

    Qiagen Filter-Tips Recalled for Leaking During Sample Preparation

    Qiagen Sciences LLC is recalling specific lots of Filter-Tips used with QIAsymphony instruments because a small percentage of tips are leaking.

    Product
    Filter-Tips, 1500 ul (1024 tips/kitbox), REF 997024- REF: 997024 IVD: Used with the QIAGEN QIAsymphony SP/AS Instruments (REF 9001297 and 9001301) REF: 997024 Used in sample preparation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1837-2019·2019-08-07

    Jubilant Cadista Recalls Drospirenone and Ethinyl Estradiol Tablets for Dissolution Failure

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Drospirenone and Ethinyl Estradiol Tablets because they failed dissolution specifications during stability testing.

    Product
    Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.02 mg, packaged into a carton containing 3 blister cards each blister card contains 28-film coated, biconvex tablets, Rx Only, Manufactured by: Cyndea Pharma, S.L., Olvega (Soria), 42110 Spain, Distributed by: Jubilant…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2127-2019·2019-08-07

    Burlington Medical Recalls Radiation Protection Caps Due to Inadequate Shielding

    Burlington Medical is recalling 49 radiation protection caps because the protective material may not adequately shield users from scatter radiation.

    Product
    Cap, Product Number Cap, Part Numbers CAP1, CAP2 Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation reaching the user.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2135-2019·2019-08-07

    Siemens Stratus CS Acute Care cTNI TestPak Recalled for False Positives

    Siemens Healthcare Diagnostics Inc is recalling Stratus CS Acute Care cTNI TestPaks due to a potential for increased false positive results.

    Product
    Stratus CS Acute Care cTNI TestPak, SMN 10445071 Product Usage: In vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma. Cardiac troponin I measurements can be used as an aid in the diagnosis of acute myocardial infarction (AMI).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2129-2019·2019-08-07

    Burlington Medical Porta Shield Radiation Protection Recall

    Burlington Medical is recalling Porta Shield radiation protection products because the material may provide inadequate protection against scatter radiation.

    Product
    Porta Shield, Product Number Porta Shield, Part Numbers PTS2, PTS3, PTS4 Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while performing fluoroscopic and radiographic procedures by reducing the amount of radiation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2114-2019·2019-08-07

    Burlington Medical Recalls 129 Full Overlap Radiation Protection Vests and Kilts

    Burlington Medical is recalling 129 two-piece radiation protection vests and kilts because the protective material may provide inadequate shielding against scatter radiation.

    Product
    2 pc Full Overlap Vest & Kilt, Single Item, Product Number FVK, Part Numbers REFVK*F, REFVK*M, REFVKB, REFVKD, REFVKE, REFVKF, SEFVK*F, SEFVK*M, SEFVKE, SEFVKXLM Product Usage: Products are designed to protect healthcare workers against scatter (secondary) radiation while…
    Category
    Medical Device
    Distribution
    Distributed nationwide