The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54751–54775 of 74002

  • HighFDA (Food)·F-1942-2015·2015-04-15

    Vitarroz Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Vitarroz Sazon seasoning packets because the cumin ingredient may contain undeclared peanut protein.

    Product
    VITARROZ SAZON CON CULANTRO Y ACHIOTE CORIANDER & ANNATTO, NET WT. 6.34 OZ. 180g, Jumbo SOBRES 36 PACKETS, UPC 0 72670 04255 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0482-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injection Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection because of crystallization. The affected vials were distributed nationwide and in Guam and Singapore.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1941-2015·2015-04-15

    Iberia Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Sazon Iberia seasoning because it may contain undeclared peanut protein. Consumers should check lot numbers and stop using the product.

    Product
    SAZON IBERIA CON CULANTRO Y ACHIOTE Coriander & Annatto: 1) NET WT. 3.52 OZ. 100g, 18/20 PACKS, UPC 0 75669 10832 9, 2) NET WT. 6.34 OZ. 180g, 15/36 PACKS, UPC 0 75669 10831 2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1394-2015·2015-04-15

    Toshiba INFX-8000V Interventional Angiography System Recall for Brake Defect

    Toshiba is recalling 28 INFX-8000V Interventional Angiography Systems because the table base rotational brake may not engage when force is applied to the table top.

    Product
    INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V224000·2015-04-15

    Thor Motor Coach Recalls 2016 Motorhomes for Missing Weight Label

    Thor Motor Coach is recalling 168 model year 2016 motorhomes because the Occupant and Cargo Carrying Capacity label may be missing water weight information, creating an overload risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR CHATEAU, OUTLAW, CITATION, SIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2015·2015-04-15

    VasoNova Vascular Positioning System G4 Console Recalled for Standard Noncompliance

    VasoNova is recalling 17 Vascular Positioning System G4 Consoles due to noncompliance with IEC Standard 60101-1-1.

    Product
    VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1379-2015·2015-04-15

    TEM Systems Recalls ROTROL P Control Vials Due to Partial Filling

    TEM Systems Inc is recalling specific lots of ROTROL P Control vials because some were found to be partially filled.

    Product
    ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0436-2015·2015-04-15

    Heritage Pharmaceuticals Recalls Gliptizide and Metformin Tablets Due to Impurity

    Heritage Pharmaceuticals is recalling specific lots of Gliptizide and Metformin HCL tablets because they failed impurity specifications. The affected bottles were distributed nationwide.

    Product
    GLIPIZIDE AND METFORMIN HCL — GLIPIZIDE AND METFORMIN HCL (GLIPIZIDE AND METFORMIN HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0435-2015·2015-04-15

    Mylan Recalls Fexofenadine HCl Tablets Due to Impurity Failures

    Mylan Pharmaceuticals is recalling specific lots of Fexofenadine HCl 60 mg tablets because they failed impurity specifications. The recall covers 13,856 bottles distributed nationwide.

    Product
    Fexofenadine HCl Tablets, USP, 60 mg, Allergy, Antihistamine, Indoor and Outdoor Allergies, Non-Drowsy, Original Prescription Strength, a) 60 count Bottles, NDC 0378-0781-91, b) 500 count Bottles, NDC 0378-0781-05, Manufactured by: Mylan Pharmaceuticals Inc, Morgantown, WV…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D00432-2015·2015-04-15

    Qualitest Recalls Promethazine VC With Codeine Syrup Due to Impurity

    Qualitest Pharmaceuticals is recalling Promethazine VC with Codeine Syrup because a stability lot failed impurity specifications.

    Product
    PROMETHAZINE VC WITH CODEINE SYRUP, EACH 5 ml contains: Codeine Phosphate 10 mg, Promethazine Hydrochloride 6.25 mg, Phenylephrine Hydrochloride 5 mg, alcohol 7%, (a) 4 fl oz bottle (NDC 0603-1588-54) and (b) 16 fl oz bottle (NDC 0603-1588-58) Rx only, Manufactured for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V219000·2015-04-14

    Gillig Recalls 2013-2015 Low Floor Buses Due to Brake Hose Wear

    Gillig is recalling 623 Low Floor transit buses from 2013-2015 because brake hoses may rub against suspension towers, potentially causing air leaks and increased stopping distances.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2015·2015-04-14

    Beech-Nut Recalls Baby Food Jars Due to Possible Glass Contamination

    Beech-Nut Nutrition is recalling approximately 1,920 pounds of Stage 2 sweet potato and chicken baby food jars due to possible glass contamination.

    Product
    Beech-Nut Nutrition Corporation — Beech-Nut Nutrition Recalls Baby Food Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15109·2015-04-14

    San Pedro Manufacturing Recalls Renovated Mattresses and Foundations

    San Pedro Manufacturing is recalling about 4,800 renovated mattresses and foundations because they fail to meet federal fire safety standards.

    Product
    Mattresses and Mattresses with Foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·060-2015·2015-04-13

    Leader Slaughterhouse Recalls Veal Carcasses Produced Without Full Federal Inspection

    Leader Slaughterhouse, LLC is recalling approximately 1,800 pounds of veal carcasses produced without the full benefit of federal inspection. The product was distributed to customers in Pennsylvania and New York.

    Product
    Leader Slaughterhouse, LLC — Leader Slaughterhouse, LLC Recalls Veal Carcasses Produced Without Full Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V215000·2015-04-13

    Crossroads Recalls 2016 Recreational Trailers Due to Wheel Stud Defect

    Crossroads is recalling 2016 recreational trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    CROSSROADS — CROSSROADS LONGHORN REZERVE, Z1, ELEVATION, HAMPTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V214000·2015-04-10

    Land Rover Recalls 2015 LR4 Models Due to ABS Software Error

    Land Rover is recalling 2015 LR4 vehicles because an ABS software error may disable stability and traction control systems, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V211000·2015-04-10

    Spartan Recalls 2015 K3 Chassis Due to Tag Axle Suspension Defect

    Spartan Motors is recalling 66 model year 2015 K3 chassis because tag axle suspension hangers may move, causing the axle to shift off center and increasing crash risk.

    Product
    SPARTAN — SPARTAN K3
    Category
    Vehicle
    Distribution
    Distributed nationwide