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.

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.

32151–32175 of 73900

  • SevereFDA (Food)·F-2162-2019·2019-09-25

    Pita Pal Foods Recalls Fresh Thyme Hummus Due to Listeria Risk

    Pita Pal Foods LP is recalling Fresh Thyme Original Hummus with Pretzels because the product has the potential to be contaminated with Listeria monocytogenes.

    Product
    Fresh Thyme Original Hummus with Pretzels 4.1 oz. UPC 41330 11210 packaged in Plastic tub with clear lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2170-2019·2019-09-25

    Pita Pal Foods Recalls Roasted Garlic Hummus Due to Listeria Risk

    Pita Pal Foods LP is recalling 840 cases of Roasted Garlic Hummus nationwide due to potential Listeria monocytogenes contamination.

    Product
    Hummus Hummus Roasted Garlic Hummus 10 oz. UPC 851351007695 packaged in Plastic tub with clear lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1869-2019·2019-09-25

    Aurolife Recalls Fexofenadine Tablets Due to Impurity Failures

    Aurolife Pharma is recalling equate Allergy Relief tablets because they failed impurity and degradation specifications.

    Product
    Allergy Relief (Fexofenadine HCl) tablets USP, 180 mg, 15-count cartons, equate, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-995-62.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1863-2019·2019-09-25

    West-Ward Recalls Oxcarbazepine Oral Suspension Due to Impurity Failures

    West-Ward Columbus Inc is recalling specific lots of Oxcarbazepine Oral Suspension because they failed impurity and degradation specifications.

    Product
    Oxcarbazepine Oral Suspension, USP, 300 mg/5 mL, 250 mL per bottle, Rx Only, Distr. by: West-Ward Pharmaceuticals,Eatontown, NJ. NDC:0054-0199-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2199-2019·2019-09-25

    PitaPal Organic Cilantro Jalapeno Hummus Recalled for Listeria Risk

    Pita Pal Foods LP is recalling PitaPal Organic Cilantro Jalapeno Hummus due to potential Listeria monocytogenes contamination.

    Product
    PitaPal Organic Cilantro Jalapeno Hummus 10 oz. UPC 851570003348 packaged in Plastic tub with clear lid with green rim.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2541-2019·2019-09-25

    Wilson-Cook Recalls Hemospray Endoscopic Hemostat Due to Misassembly

    Wilson-Cook Medical Inc. is recalling 160 units of Hemospray Endoscopic Hemostat because misassembly may prevent the device from spraying powder.

    Product
    Hemospray Endoscopic Hemostat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V679000·2019-09-25

    Volkswagen Recalls Multiple Models Due to Regulatory Non-Compliance

    Volkswagen is recalling specific 2007-2019 models because internal evaluation modifications may cause non-compliance with regulatory requirements, potentially increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, PASSAT, JETTA HYBRID, BEETLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2543-2019·2019-09-25

    Boston Scientific Recalls S-ICD Devices Due to Battery Depletion

    Boston Scientific is recalling 404 EMBLEM MRI S-ICD devices because a compromised electrical component causes accelerated battery depletion, potentially requiring earlier replacement.

    Product
    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2542-2019·2019-09-25

    Boston Scientific Recalls 28 Subcutaneous Implantable Cardioverter Defibrillators

    Boston Scientific is recalling 28 EMBLEM S-ICD devices due to accelerated battery depletion. Patients should contact their healthcare provider for evaluation.

    Product
    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEMTM S-ICD Pulse Generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2547-2019·2019-09-25

    Philips IntelliVue Remote Antenna Cable Recalled for Incorrect Rating

    Philips is recalling IntelliVue 1.4 GHz Remote Antenna cables used with MX40 monitors because they lack the required rating for some installations.

    Product
    IntelliVue 1.4 GHz Remote Antenna Used with Philips MX4O Monitors-The affected product is a 74 foot (22.6m) combined coax and unshielded twisted pair data cable bundle and is a component of the Philips Remote Antenna (PN 867151). The Remote Antenna is used with IntelliVue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1862-2019·2019-09-25

    Torrent Pharma Recalls Anagrelide Capsules Due to Impurity Failures

    Torrent Pharma Inc. is recalling 2,472 bottles of Anagrelide Capsules because routine stability testing detected high levels of impurities.

    Product
    ANAGRELIDE — ANAGRELIDE (ANAGRELIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1870-2019·2019-09-25

    Aurolife Pharma Recalls Fexofenadine Hydrochloride Tablets for Impurity Failures

    Aurolife Pharma is recalling specific lots of 180 mg Fexofenadine Hydrochloride tablets because they failed impurity and degradation specifications.

    Product
    Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 62011-0315-1); and b) 30-count cartons (NDC 62011-0315-2) HealthMart PHARMACY, Distributed by McKesson, One Post Street, San Francisco, CA 94104.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1865-2019·2019-09-25

    Aurolife Pharma Recalls Allergy Relief Tablets Due to Impurity Failures

    Aurolife Pharma is recalling specific lots of Allergy Relief (Fexofenadine Hydrochloride) 180 mg tablets because they failed impurities and degradation specifications.

    Product
    Allergy Relief (Fexofenadine Hydrochrloride) Tablets USP, 180 mg, packaged in a) 15-count cartons (NDC 60000-409-53); b) 30-count cartons (NDC 60000-409-30); c) 45-count bonus cartons (NDC 60000-409-48); d) 45-count cartons (NDC 60000-409-45); CAREone, Distributed by: Foodhold…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2545-2019·2019-09-25

    CooperSurgical Recalls LEEP Return Patient Pads Due to Expiration Date Errors

    CooperSurgical is recalling LEEP Return Patient Pads because the expiration dates on the outer boxes have the month and day reversed compared to the individual pouches.

    Product
    LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V676000·2019-09-23

    Mercedes-Benz Recalls E-Class Wagons Due to Rear Spoiler Detachment Risk

    Mercedes-Benz is recalling specific 2017-2019 E-Class wagons because the rear spoiler may detach while driving, creating a road hazard and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, E63S, E 400, E400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V674000·2019-09-23

    Spartan Metrostar and Gladiator Recall for Air Brake Control Line Defect

    Spartan is recalling 2004-2020 Metrostar and Gladiator vehicles because unprotected air brake control lines may cause unexpected brake application and increase crash risk.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V673000·2019-09-23

    Pleasure Way Recalls 2018-2020 Motorhomes for Awning Drive Mechanism Failure

    Pleasure Way is recalling 2018-2020 Plateau, Ascent, and Lexor motorhomes because the awning drive mechanism may fail, causing the awning to extend unexpectedly.

    Product
    PLEASURE WAY — PLEASURE WAY PLATEAU, LEXOR, ASCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V668000·2019-09-20

    Forest River Recalls 2020 Cherokee Trailers Due to Wiring Exposure

    Forest River is recalling 2020 Cherokee trailers because missing protective paneling exposes distribution panel wiring, increasing the risk of electrical shock or fire.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V675000·2019-09-20

    Ducati Recalls 2014-2018 Motorcycles Due to Engine Oil Leak Risk

    Ducati is recalling 651 motorcycles because engine oil may leak into the airbox and drip onto the rear tire, increasing crash risk.

    Product
    DUCATI — DUCATI PANIGALE R, 1299, 1199
    Category
    Vehicle
    Distribution
    Distributed nationwide