The Recall Desk

State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28051–28075 of 73762

  • HighFDA (Devices)·Z-2767-2020·2020-08-12

    Boss Instruments Recalls DeBakey Needle Holders Due to Plate Breakage Risk

    Boss Instruments is recalling 96 DeBakey needle holders because the tungsten carbide plate can break under pressure, posing a risk to patients and medical staff.

    Product
    BOSS DeBakey "Gator-Grip" Needle Holder 2 mm tip, 9", Part Numbers 50-2503 and 51-2503 - Product Usage: Endoscopic cleaning brushes are single use devices intended to clean the interior of endoscopes after endoscopy procedures. The brush is threaded through the biopsy valve and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2748-2020·2020-08-12

    Teleflex Pleur-Evac Chest Drainage Devices Recalled for Packaging Risk

    Teleflex Medical Inc. is recalling Pleur-Evac chest drainage devices because sterile packaging may be compromised, potentially affecting sterility.

    Product
    Pleur-Evac Adult-Ped Wet, LF Intl Eng, product code: A-8000I - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2754-2020·2020-08-12

    BD MAX SARS-CoV-2 Reagents Recalled for Potential False Positive Results

    Becton Dickinson is recalling BD MAX SARS-CoV-2 Reagents due to elevated rates of potential false positive results, which could delay diagnosis and increase exposure risk.

    Product
    BD MAX SARS-CoV-2 Reagents, Cat. No. 445003 (UDI 00382904450038) and 445003-01 (UDI (01)603829044500301) - Product Usage: intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal, nasal, mid-turbinate, and oropharyngeal swab specimens…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2756-2020·2020-08-12

    Siemens Luminos Agile Max Recalled for Software Collision and Image Errors

    Siemens Medical Solutions is recalling 477 Luminos Agile Max units due to software defects that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2757-2020·2020-08-12

    Siemens Uroskop Omnia Max Recalled for Software Collision and Image Errors

    Siemens is recalling 194 Uroskop Omnia Max units due to software issues that may cause system collisions or incorrect diagnostic images.

    Product
    SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20162·2020-08-12

    Intertex Recalls B-Air, BlueDri, and Soleaire Blowers Due to Fire Hazard

    Intertex is recalling approximately 189,000 B-Air, BlueDri, BlueDri Pro, and Soleaire blowers because unprotected side outlets pose a fire hazard.

    Product
    B-Air, BlueDri, BlueDri Pro and Soleaire Blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2753-2020·2020-08-12

    Randox Lipase Assay Substrate Recalled for Imprecision in Quality Control

    Randox Laboratories is recalling specific batches of Lipase R2 Substrate due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric R2 Substrate - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2749-2020·2020-08-12

    Teleflex Pleur-Evac Chest Drainage Devices Recalled for Packaging Compromise

    Teleflex Medical Inc. is recalling Pleur-Evac chest drainage devices because sterile packaging may be compromised, potentially affecting sterility.

    Product
    Pleur-Evac Adult-Ped Wet, LF Eng/Spanish, product code: A-8000I-06 - Product Usage: CHEST DRAINAGE: To evacuate air and/or fluid from the chest cavity or mediastinum. To help prevent air and/or fluid from re-accumulating in the chest cavity or mediastinum. To help re-establish…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2747-2020·2020-08-12

    Siemens DCA Vantage Barcode Scanner Recalled for Data Integrity Issues

    Siemens Healthcare is recalling 1,800 DCA Vantage Handheld Barcode Scanners because they may fail to verify check digits or incorrectly process barcodes, potentially leading to data errors.

    Product
    DCA Vantage Handheld Barcode Scanner - Zebra Model - Model # DS4308 - HC0015BZZWW external accessory to DCA Vantage Analyzer US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2752-2020·2020-08-12

    Randox Lipase Assay Buffer Recalled for Imprecision in Quality Control

    Randox Laboratories is recalling specific batches of Lipase Colorimetric R1 Buffer due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric R1 Buffer - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1487-2020·2020-08-12

    Vilvet Pharmaceuticals Recalls VILAMIT MB Due to cGMP Deviations

    Vilvet Pharmaceuticals is recalling 11,640 bottles of VILAMIT MB capsules due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and nationwide.

    Product
    VILAMIT MB (118 mg methenamine, 36 mg phenyl salicylate, 40.8 mg sodium phosphate monobasic, 10.0 mg methylene blue and 0.12 mg hyoscyamine sulfate), Rx Only, 100 Capsules per Bottle, Manufactured for: Vilvet Pharmaceuticals Inc., Chester Springs, PA 18425, NDC 71186-002-35.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2751-2020·2020-08-12

    Randox Lipase Assay Reagent Recalled for Imprecision in Quality Control and Patient Samples

    Randox Laboratories is recalling specific batches of Lipase Colorimetric Reagent due to confirmed imprecision in quality control and patient samples.

    Product
    Randox Lipase Assay: Lipase Colorimetric Reagent - Product Usage: A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2744-2020·2020-08-12

    Sutter Swyng Non-Stick Bipolar Forceps Recalled for Incorrect Package Insert Labeling

    Sutter Medizintechnik GmbH is recalling 1,337 units of Sutter Swyng non-stick bipolar forceps because the package insert incorrectly displays the Ethylene Oxide sterilization symbol instead of the irradiation symbol.

    Product
    Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps are provided with bayonet-style handle design with straight or angled tips and different total lengths. They are to be connected through an appropriate bipolar…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1488-2020·2020-08-12

    Vilvet Pharmaceuticals Recalls VILEVEV MB Urinary Antiseptic Due to cGMP Deviations

    Vilvet Pharmaceuticals is voluntarily recalling 1,716 bottles of VILEVEV MB Urinary Antiseptic due to current Good Manufacturing Practice (cGMP) deviations.

    Product
    VILEVEV MB Urinary Antispetic (81.0 mg methenamine, 40.8 mg sodium phosphate monobasic and 10.8 mg methylene blue, 0.12 mg hyoscyamine sulfate and 32.4 mg phenyl salicylate), Rx Only, 90 Tablets per Bottle, Manufactured for: Vilvet Pharmaceuticals, Inc., Chester Springs, PA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1143-2020·2020-08-12

    Vitamin Shoppe Recalls Calcium Citrate Plus Magnesium & Vitamin D Supplements

    Vitamin Shoppe is recalling specific bottles of Calcium Citrate Plus Magnesium & Vitamin D because sample analysis revealed the product is sub-potent for Vitamin D.

    Product
    The Vitamin Shoppe Calcium Citrate Plus Magnesium & Vitamin D. 100 count (VS-1086; UPC:6653601086), 300 count (VS-1087; UPC: 6653601087), and 600 count (VS-1123; UPC: 6653601123).
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V472000·2020-08-11

    Triumph Recalls 2019-2020 Motorcycles Due to Wiring Harness Defect

    Triumph is recalling 2019-2020 Street Scrambler and Street Twin motorcycles because a misrouted wiring harness may contact the frame, causing the engine to stall and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH STREET SCRAMBLER, STREET TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V471000·2020-08-10

    BMW Recalls Motorcycles Due to Fuel Pump Flange Crack Risk

    BMW is recalling specific motorcycles because a fuel pump flange may crack, causing a fuel leak that increases fire risk.

    Product
    BMW — BMW K1200 GT, HP2 SPORT, K1200 S, K1200 R SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2020·2020-08-10

    Mr. Wok Foods Recalls Meat and Poultry for Undeclared Allergens

    Mr. Wok Foods is recalling approximately 242,640 pounds of frozen meat and poultry products due to misbranding and undeclared allergens.

    Product
    Mr Wok Foods Inc. dba Maxfield Foods — Mr. Wok Foods, Inc. Recalls Multiple Meat and Poultry Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V470000·2020-08-10

    Ford Recalls 2020 Lincoln Corsair for Rear Coil Spring Clearance Issue

    Ford is recalling 2,965 2020 Lincoln Corsair vehicles because rear coil springs may lack sufficient clearance, potentially breaking and affecting vehicle handling.

    Product
    LINCOLN — LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20T015000·2020-08-10

    Linglong Americas Recalls Venezia Crusade HT Tires Due to Sidewall Separation

    Linglong Americas Inc. is recalling specific Venezia Crusade HT tires because they may experience lower sidewall separation, which can lead to sudden tire failure and increase the risk of a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V467000·2020-08-10

    Ford Recalls 2020 F-150 Trucks Due to Starter Motor Fire Risk

    Ford is recalling 2020 F-150 vehicles because an incorrect attachment nut on the starter motor may cause electrical arcing and increase the risk of a fire.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E054000·2020-08-10

    Kiel Recalls Avance Passenger Seats Due to Seat Belt Defect

    Kiel is recalling specific Avance passenger seats for motorcoaches because the seat belt retractors may not function properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide