The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57601–57625 of 74005

  • ModerateFDA (Drugs)·D-1520-1014·2014-08-13

    FDA Recalls Unapproved Vitamin B12 Injections Due to Unregistered Manufacturer

    Medical Supply Liquidators LLC is recalling Vitamin B12 Methylcobalamin Injections because the manufacturer is not registered with the FDA and the product lacks an approved NDA or ANDA.

    Product
    Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml, Sterile, 10 ml vial and 30 ml vial. For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1522-2014·2014-08-13

    FDA Recalls Unapproved Vitamin B12 Injection Vials Nationwide

    Medical Supply Liquidators LLC is recalling Vitamin B12 Cyanocobalamin Injection vials because the manufacturer is not FDA-registered and the product lacks an approved NDA/ANDA.

    Product
    Vitamin B12 Cyanocobalamin Injection USP 1000 mcg/ml, Sterile, 10 ml vial and 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2144-2014·2014-08-13

    Zimmer Recalls Tapered Screw-Vent Dental Implant Due to Labeling Error

    Zimmer, Inc. is recalling Tapered Screw-Vent Dental Implants because the inner vial is labeled with incorrect dimensions.

    Product
    Tapered-Screw Vent Implant, HA, 4.7mmD x 8mmL x 4.5mm, Part No. TSVWH8 Dental implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2147-2014·2014-08-13

    Boston Scientific recalls 21 ENDOTAK RELIANCE defibrillation leads due to test errors

    Boston Scientific is recalling 21 ENDOTAK RELIANCE defibrillation leads because manufacturing test records showed suspected data recording errors. No injuries have been reported.

    Product
    Boston Scientific ENDOTAK RELIANCE¿ SG, transvenous defibrillation lead, Models 0180 & 0292, Sterile EO. Product Usage: The ENDOTAK RELIANCE leads provide pacing and rate-sensing and deliver cardioversion and defibrillation shocks for automatic implantable cardioverter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1513-2014·2014-08-13

    Wockhardt Recalls BuPROPion HCl Extended-Release Tablets Due to Impurity Levels

    Wockhardt USA is recalling 840 bottles of buPROPion HCl Extended-Release Tablets because out-of-specification levels of the impurity m-chlorobenzoic acid were observed.

    Product
    buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 500-count bottle, Rx Only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA, LLC, 20 Waterview Blvd, Parsippany, NJ 07054 USA, NDC 64679-101-07.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1510-2014·2014-08-13

    Caraco Recalls Cephalexin Capsules Due to Manufacturing Deviations

    Caraco Pharmaceutical is recalling Cephalexin Capsules, 250 mg, because the active ingredients were not manufactured with good manufacturing practices.

    Product
    Cephalexin Capsules, USP, 250 mg, packaged in a) 100-count bottles (NDC 62756-293-88) and b) 500-count bottles (NDC 62756-293-13), Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd., Acme Plaza, Andheri-Kurla Road, Andheri (East), Mumbai-400 059, India.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1527-2014·2014-08-13

    FDA Recalls Unapproved Vitamin B12 Injection Vials Nationwide and Abroad

    Medical Supply Liquidators LLC is recalling Vitamin B12 Cyanocobalamin injections because the manufacturer is not FDA-registered and the product lacks an approved NDA or ANDA.

    Product
    Vitamin B12 Cyanocobalamin with MIC Injection USP 1000 mcg/ml, packaged in 10 ml vials and 30 ml vials, Sterile, for IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1525-2014·2014-08-13

    Medical Supply Liquidators Recalls Unapproved MIC Injection Vials

    Medical Supply Liquidators LLC is recalling MIC Injection USP vials because the manufacturer is not registered with the FDA and the product lacks an approved NDA/ANDA.

    Product
    MIC Injection USP, Sterile, 10 ml vial and 30 ml vial, For IM or Deep SQ Use, Multiple Dose Vial, Manufactured by: CB Inc. for Sunshine Labs, www.sunshinelabs.us
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2150-2014·2014-08-13

    Siemens ADVIA Centaur CP BNP Kit Recalled for Failed Calibration

    Siemens Healthcare Diagnostics is recalling 961 BNP kits due to complaints of failed calibration. The kits are used for in vitro diagnostic testing of B-type Natriuretic Peptide.

    Product
    SIEMENS ADVIA Centaur CP Immunoassay System BNP kit; SMN 10309045 - 500 test For in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the ADVIA Centaur CP System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2154-2014·2014-08-13

    Teleflex Recalls RUSCH Foley Urinary Catheter Insertion Trays Due to Labeling Error

    Teleflex Medical is recalling 720 RUSCH Foley Urinary Catheter Insertion Trays because the expiration date is incorrectly printed as the same as the manufacturing date.

    Product
    RUSCH Foley Urinary Catheter Insertion Tray with 10cc syringe, BZK Swabs, Sterile, Rx only, Teleflex Medical Product Code: 76730.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1516-2014·2014-08-13

    Novartis Recalls Cataflam Tablets Due to Illegible Ink Identification

    Novartis is recalling 50 bottles of Cataflam (diclofenac potassium) 50 mg tablets because ink identification rubbed off during transit, making them illegible.

    Product
    Cataflam (diclofenac potassium) tablets, 50 mg, 100-count bottles, Rx only, Manufactured by: Patheon Inc., Whitby Operations, Ontario, Canada L1N 5Z5; Distributed by: Novartis Pharmaceuticals Corp., East Hanover, New Jersey 07936; NDC 0078-0436-05, UPC 3 0078-0436-05 2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V705000·2014-08-12

    Blue Bird Recalls 2015 School Buses Due to Fuel Filter Defect

    Blue Bird is recalling 2015 All American and Vision school buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T010000·2014-08-12

    TBC Recalls Wild Country Radial Tires Due to Sidewall Cracking

    TBC Corporation is recalling specific Wild Country Radial XTX Sport tires due to sidewall cracking that could lead to sudden air loss and a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14254·2014-08-12

    CoScentrix Recalls DD Brand Tin Candles Due to Fire Hazard

    CoScentrix is recalling DD Brand tin candles sold at Hobby Lobby because the high flame can ignite the wax and container, posing a fire hazard.

    Product
    DD Brand Tin Candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·052-2014·2014-08-12

    Applegate Recalls Chicken Nuggets Due To Possible Plastic Contamination

    Applegate is recalling frozen chicken nuggets due to possible plastic contamination. No illnesses or injuries have been reported.

    Product
    Gold Creek Foods, LLC — Georgia Firm Recalls Chicken Nugget Product Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14T009000·2014-08-11

    Continental Recalls Motorcycle Tires Due to Tread Separation Risk

    Continental is recalling specific motorcycle tires because the tread, belt, and carcass may separate, causing a loss of inflation pressure and increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V496000·2014-08-11

    Versalift Recalls Ford Super Duty Trucks with Fire Risk

    Versalift is recalling 2009-2013 Ford Super Duty trucks equipped with specific PTO assemblies due to a risk of fire from oil leaking onto the exhaust.

    Product
    FORD — FORD F-550 SUPER DUTY, F-350 SUPER DUTY, F-450 SUPER DUTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V495000·2014-08-11

    Ford Recalls 2013-2014 Focus and Escape Vehicles for Wiring Defect

    Ford is recalling 2013-2014 Focus ST and Escape vehicles with 2.0-liter engines because a wiring defect may cause the engine to stall, increasing crash risk.

    Product
    FORD — FORD FOCUS, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·051-2014·2014-08-09

    Oberto's Recalls Chicken Strips Due to Quality Control Issues

    Oberto's Brands is recalling approximately 57,578 pounds of chicken strips due to a company quality issue involving increased water activity.

    Product
    Recall Notification Report 051-2014
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E052000·2014-08-08

    Lippert Recalls Recreational Vehicle Frames With Defective Spring Hangers

    Lippert is recalling certain recreational vehicle frames manufactured in February 2014 because the spring hangers may fracture, potentially causing loss of vehicle control.

    Product
    STRUCTURE:FRAME AND MEMBERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V490000·2014-08-08

    General Motors Recalls 2002-2004 Saturn Vues for Ignition Key Defect

    General Motors is recalling 2002-2004 Saturn Vues because the key may be removed from the ignition while the vehicle is not in the Off position, creating a risk of the vehicle rolling away.

    Product
    SATURN — SATURN VUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V488000·2014-08-08

    GM Recalls 2013 Buick Encore and Cadillac ATS for Seat Belt Defect

    General Motors is recalling 2013 Buick Encore and Cadillac ATS vehicles because front lap belt pretensioner cables may not lock, increasing injury risk in a crash.

    Product
    CADILLAC — CADILLAC, BUICK ATS, ENCORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V491000·2014-08-08

    All Wheel Recalls 2011-2012 Ford F-550 Chassis Due to Fire Risk

    All Wheel is recalling 2011-2012 Ford F-550 Super Duty chassis with 6.8L gasoline engines due to a PTO oil leak that poses a fire risk.

    Product
    SUPER DUTY — SUPER DUTY F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V489000·2014-08-08

    GM Recalls 2014-2015 Chevrolet Impala for Storage Console Latch Defect

    General Motors is recalling 2014-2015 Chevrolet Impala vehicles because the center storage console may not stay latched during a crash, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET IMPALA
    Category
    Vehicle
    Distribution
    Distributed nationwide