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.

33351–33375 of 73900

  • ModerateFDA (Devices)·Z-1801-2019·2019-06-26

    Arrowg+ard Blue Advance JACC Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling Arrowg+ard Blue Advance JACC products due to an incorrect expiration date. The recall involves 174 units distributed nationwide.

    Product
    Arrowg+ard Blue Advance JACC Product Code: CDC 42063 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1387-2019·2019-06-26

    Sun Pharmaceutical Recalls Allergy Relief D Tablets Due to Impurities

    Sun Pharmaceutical is recalling Allergy Relief D tablets because testing showed impurities and degradation levels above or near specification limits.

    Product
    Allergy Relief D, Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg, Extended Release Tablets, USP, 30-count box, Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895. Made in India. UPC 0 50428 39131 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1805-2019·2019-06-26

    Arrow PICC with Chloraguard Technology Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 135 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.

    Product
    Arrow¿ PICC with Chlorag+ard Technology Product Code: CDC 44052 HPK1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1821-2019·2019-06-26

    Arrow PICC with Chloraguard Technology Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 578 units of Arrow PICC with Chloraguard Technology due to an incorrect expiration date.

    Product
    Arrow¿ PICC with Chlorag+ard¿ Technology Product Code: PR 45552 HPHNL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1843-2019·2019-06-26

    Cytocell Aquarius D13S319 Probe Recalled for Package Insert Error

    Cytocell Ltd. is recalling Aquarius D13S319 Plus Deletion Probes because the chromomap on the package insert contains an error.

    Product
    Aquarius D13S319 Plus Deletion Probe, Model LPH068-A Product Usage: The D13S319 probe, labelled in red, covers a 156kb region including most of the DLEU2 gene, part of the DLEU1 gene and the D13S319 and D13S272 markers. The 13qter subtelomere specific probe, labelled in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1392-2019·2019-06-26

    Akorn Recalls Myorisan Isotretinoin Capsules Due to Labeling Error

    Akorn Inc. is recalling 16,216 cartons of Myorisan isotretinoin capsules because secondary cartons incorrectly state 40 mg instead of 30 mg.

    Product
    Myorisan (isotretinoin capsules, USP), 40 mg, packaged in cartons of 30 Capsules containing 3 x 10 Prescription Packs, Rx Only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forest, IL 60045, NDC 61748-304-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1804-2019·2019-06-26

    Arrow JACC Central Catheter Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 12 units of JACC central catheters because the expiration date printed on the packaging is incorrect.

    Product
    Arrow¿ JACC with Chlorag+ard¿ Technology Jugular Axillosubclavian Central Catheter Product Code: CDC 43063 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1802-2019·2019-06-26

    Arrow JACC Central Catheter Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 6 units of Arrow JACC Central Catheters because the expiration date is incorrect.

    Product
    Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42552 JX1A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1391-2019·2019-06-26

    Teligent Pharma Recalls Betamethasone Dipropionate Ointment Due to Impurities

    Teligent Pharma is recalling Betamethasone Dipropionate Ointment 0.05% due to failed impurities and degradation specifications.

    Product
    Betamethasone Dipropionate Ointment USP, 0.05%* (Augmented), a) 15 gram (NDC 52565-019-15) and b) 50 gram (NDC 52565-019-51) tubed, Rx Only, Manufactured by: Teligent Pharma, Inc. Buena, New Jersey 06310
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1815-2019·2019-06-26

    Arrow JACC Medical Device Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 3 units of Arrow JACC with Chloragard Technology due to an incorrect expiration date.

    Product
    Arrow¿ JACC with Chlorag+ard Technology Product Code:JR 42563 HPHNM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V489000·2019-06-25

    Mercedes-Benz Metris Recalled for Potential Loss of Power Steering

    Daimler Vans USA is recalling 2018-2019 Mercedes-Benz Metris vehicles because a steering sensor defect may cause the electric power steering assist to deactivate, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19145·2019-06-25

    QTOP USA Recalls LED Work Light Bulbs Due to Fire Hazard

    QTOP USA is recalling specific LED work light replacement bulbs because they can overheat and cause fires. Consumers should stop using the bulbs and contact the company for a refund.

    Product
    LED Work Light Replacement Bulbs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19146·2019-06-25

    West Marine Recalls Folding Deck Chairs Due to Fall and Injury Hazards

    West Marine is recalling about 11,600 folding deck chairs because a lock nut can loosen, posing fall and injury hazards. No injuries have been reported.

    Product
    West Marine Deck chairs and Comfort Plus Deck Crew folding chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V488000·2019-06-24

    Mazda Recalls 2010-2011 RX-8 Vehicles for Air Bag Inflator Defect

    Mazda is recalling 2010-2011 RX-8 vehicles because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V485000·2019-06-21

    Oshkosh Recalls 2019 McNeilus Front Loader Trucks Due to Fire Risk

    Oshkosh is recalling 2019 McNeilus Meridian, Atlantic, and Contender front loader trucks because battery cables may rub against the fuse box bracket, increasing the risk of fire.

    Product
    MCNEILUS — MCNEILUS MERIDIAN FRONT LOADER, ATLANTIC FRONT LOADER, CONTENDER FRONT LOADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V484000·2019-06-21

    Oshkosh Recalls 2018 McNeilus Concrete Mixers for Tank Rupture Risk

    Oshkosh is recalling 2018 McNeilus Bridgemaster V Concrete Mixers because an incorrect filler neck part may cause the tank to overpressurize and rupture.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V483000·2019-06-21

    Altec Aerial Devices Recalled for Air Brake System Defects

    Altec is recalling 2003-2019 aerial devices due to potential air brake pressure loss. Owners should contact dealers for free inspection and repair.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V486000·2019-06-21

    Oshkosh Recalls 2018-2019 S-Series Mixers Due to Steering Hose Error

    Oshkosh is recalling 2018-2019 S-Series Mixer vehicles because hydraulic hoses may be installed incorrectly, causing loss of steering assist and increasing crash risk.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V481000·2019-06-21

    Forest River Recalls 2019-2020 Motorhomes Due to Slide-Out Defect

    Forest River is recalling 2019-2020 Georgetown and FR3 motorhomes because slide-out mechanisms may activate unintentionally, increasing injury risk.

    Product
    FOREST RIVER — FOREST RIVER FR3, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V476000·2019-06-21

    Forest River Recalls 2017-2020 Recreational Trailers for Electrical Safety

    Forest River is recalling 2017-2020 Shasta and Coachmen recreational trailers because exterior kitchen outlets may lack GFCI protection, posing an electrical shock risk.

    Product
    SHASTA — SHASTA, COACHMEN PHOENIX, CHAPARRAL X-LITE, CHAPARRAL LITE, CHAPARRAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V478000·2019-06-21

    Navistar Recalls 2011 IC Bus School Buses for Seat Belt Defect

    Navistar is recalling 2011 IC Bus RE, CE, and BE school buses because plastic parts on non-retractable seat belt buckles may crack, making them difficult to fasten.

    Product
    IC BUS — IC BUS RE, CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide