The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58601–58625 of 74011

  • ModerateFDA (Drugs)·D-1284-2014·2014-05-07

    Caraco Recalls Venlafaxine Hydrochloride Extended-Release Tablets for Dissolution Failure

    Caraco Pharmaceutical Laboratories is recalling 91,777 bottles of Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, because stability results showed the product did not meet drug release dissolution specifications.

    Product
    Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, packaged in a) 30-count bottles (NDC 41616-760-83, UPC 3 41616 76083 5); and b) 90-count bottles (NDC 41616-760-81, UPC 3 41616 76081 1), Rx only, Distributed by: Caraco Pharmaceutical Laboratories, Ltd., 1150 Elijah…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1524-2014·2014-05-07

    Medtronic Neurostimulators Recalled for Cycling Feature Labeling Concerns

    Medtronic is recalling specific neurostimulators because current labeling indicates the cycling feature improves device longevity, a claim that may be inaccurate.

    Product
    Medtronic neurostimulators. Restore (37711), RestoreADVANCED (37713), RestoreADVANCED SureScan MRI (97713), RestoreSENSOR (37714), RestoreSENSOR SureScan MRI (97714), PrimeAdvanced SureScan MRI, (97702), RestoreULTRA (37712), RestoreULTRA SureScan MRI (97712), Itrel 4 (37703)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1280-2014·2014-05-07

    Teva Recalls Fluoxetine Capsules Due to Chemical Contamination and Odor

    Teva Pharmaceuticals is recalling Fluoxetine Capsules due to a customer complaint trend regarding capsule odor, indicating chemical contamination.

    Product
    FLUOXETINE — FLUOXETINE (FLUOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1298-2014·2014-05-07

    P&L Developments Recalls Children's Cold and Cough Liquid for Precipitate

    P&L Developments is recalling 1,363,338 bottles of Children's Triacting Night Time Cold & Cough with PE because small amounts of diphenhydramine and mannitol precipitated out of solution.

    Product
    Children's Triacting Night Time Cold & Cough with PE (diphenhydramine hcl and phenylephrine hcl), Grape Flavor, For Ages 6 to 11, 4 fl oz Bottles, liquid. Labeled A) aaron health KIDS, Manufactured by: Aaron Industries, P.O. Box 801, Lynwood, CA 90262. UPC: 7 15256 72204 9. B)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1290-2014·2014-05-07

    AbbVie Recalls Lupron Depot Kits With Defective Needle Protection

    AbbVie is recalling 1,530 Lupron Depot kits because some may contain a syringe with a defective needle stick protection device.

    Product
    LUPRON DEPOT — LUPRON DEPOT (LEUPROLIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1286-2014·2014-05-07

    Aaron Industries Recalls Tussin DM Cough Syrup Due to Precipitate

    Aaron Industries is recalling 108,792 bottles of Tussin DM cough syrup because a white substance, identified as the active ingredient Guaifenesin, was observed in some bottles.

    Product
    Maximum Strength/Non-Drowsy Tussin DM Adult Maximum Strength, Cough Cold, Dextromethorphan HBr, USP, 10 mg (Cough Suppressant) , Guaifenesin, USP, 200 mg (Expectorant), 4, 8 fl oz bottles , OTC only, labeled as A) CareOne 8 fl oz bottle, Distributed by American Sales Company…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1299-2014·2014-05-07

    Apotex Recalls Risperidone Oral Solution Due to Impurity Specification Failure

    Apotex Inc. is recalling Risperidone Oral Solution because it failed impurity specifications at the 18-month stability time point.

    Product
    Risperidone Oral Solution, 1 mg/mL, 30 mL bottle, Rx only, Manufactured by Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for Apotex Corp., Weston, FL 33326, NDC 60505-0380-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1285-2014·2014-05-07

    Glytone Acne Facial Cleanser Recalled for Viscosity Specification Failure

    Genesis Pharmaceuticals is recalling 461 bottles of Glytone Acne Treatment Facial Cleanser due to out-of-specification viscosity results.

    Product
    Glytone Acne, acne treatment facial cleanser, 2% Salicylic Acid, 200 mL/6.7 FL Oz Bottle, Distributed by Genesis Pharmaceuticals, Inc. a subsidiary of Pierre Fabre, Parsippany, NJ 07054, UPC 3 04760-00413-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1296-2014·2014-05-07

    Caraco Recalls Cetirizine Hydrochloride Chewable Tablets Due to Impurities

    Caraco Pharmaceutical Laboratories is recalling specific lots of Cetirizine Hydrochloride Chewable Tablets because they failed impurity testing.

    Product
    Cetirizine Hydrochloride Chewable Tablets, 5 mg, 30 count bottle, OTC Manufactured by Sun Pharma, Gujarat, India, NDC 47335-343-83
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·14168·2014-05-05

    Cannondale Recalls 2014 Tandem Bicycles Due to Fork Breakage Risk

    Cycling Sports Group is recalling about 80 2014 Cannondale tandem bicycles because the fork can break, causing riders to lose control and potentially be injured.

    Product
    2014 Cannondale Tandem Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V231000·2014-05-02

    Federal Coach Recalls 2010 Spirit and Premier Buses for Fire Risk

    Federal Coach is recalling 2010 Spirit and Premier buses because voltage spikes may damage door actuator circuit boards, increasing the risk of fire.

    Product
    FEDERAL COACH — FEDERAL COACH SPIRIT, PREMIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V229000·2014-05-02

    Nissan Recalls 2014 Pathfinder, Rogue, and Infiniti QX60 for Loose Lug Nuts

    Nissan is recalling 2014 Pathfinder, Rogue, and Infiniti QX60 vehicles because a right-side lug nut may not be properly tightened, posing a wheel separation risk.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V230000·2014-05-02

    Ferrara Intruder Ember Cab and Chassis Seat Belt Recall

    HME, Inc. is recalling one 2013 Ferrara Intruder Ember emergency vehicle because the seat belt latch plate can become partially engaged, making it difficult to unlatch.

    Product
    FERRARA — FERRARA INTRUDER EMBER CAB/CHASSI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V256000·2014-05-02

    Trans Tech Recalls 2013 School Buses with Wheelchair Lift Fire Risk

    Trans Tech Bus is recalling 2013 SC139DSFP500 school buses equipped with specific Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.

    Product
    TRANS TECH — TRANS TECH SC139DSFP500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V228000·2014-05-01

    Coach and Equipment Recalls 2013 Metro Lite and Phoenix Buses

    Coach and Equipment is recalling 2013 Metro Lite and Phoenix buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT METRO LITE, PHOENIX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V227000·2014-05-01

    Polaris Recalls Victory Motorcycles Due to Engine Seizure Risk

    Polaris is recalling specific 2014-2015 Victory motorcycles because an engine defect may cause the engine to seize, increasing the risk of a crash.

    Product
    VICTORY — VICTORY GUNNER, VISION, VEGAS EIGHT BALL, BOARDWALK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14733·2014-05-01

    Altria Recalls 3-in-1 Flashlight Due to Burn and Injury Hazards

    Altria Group Distribution Company is recalling 365,000 Marlboro promotional flashlights because matches can ignite inside the device, posing burn and injury risks.

    Product
    3-in-1 flashlight, compass and match holder
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14732·2014-05-01

    J. Crew Recalls Baby Coveralls Due to Choking Hazard

    J. Crew is recalling approximately 8,700 baby coveralls because snaps can detach, posing a choking hazard to young children.

    Product
    Baby Coveralls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1880-2014·2014-04-30

    Frontier and Simply Organic Black Peppercorns Recalled for Salmonella

    Frontier Natural Products Co-op is recalling various brands of organic whole black peppercorns because testing revealed the presence of Salmonella.

    Product
    1) Frontier Natural Products Co-op, Whole Black Peppercorns, Certified Organic, Piper nigrum. Net 11.3 Kg 25 LB. Packaged in corrugated cardboard boxes. Firm name on the label is Frontier in Norway, IA. UPC 0-89836-82603-9.; 2) Frontier Natural Products Co-op, Whole Black…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1251-2014·2014-04-30

    Shire Recalls VPRIV Vials Due to Presence of Particulate Matter

    Shire Human Genetic Therapies is recalling 8,359 vials of VPRIV (velaglucerase alfa) because they contain stainless steel and barium sulfate particles.

    Product
    VPRIV — VPRIV (VELAGLUCERASE ALFA)
    Category
    Drug
    Distribution
    Distributed nationwide