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.

55676–55700 of 74005

  • ModerateFDA (Devices)·Z-0939-2015·2015-01-14

    Baxter HomeChoice Automated Peritoneal Dialysis Systems Recalled for Updated Warnings

    Baxter Healthcare is recalling HomeChoice and HomeChoice Pro Automated Peritoneal Dialysis systems because the patient guide lacks updated warnings and cautions.

    Product
    HomeChoice Automated PD system and HomeChoice Pro Automated PD system Baxter's HomeChoice and HomeChoice Pro APD systems are designed to provide Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients. Their Fill volumes can range from 60 mL to 3000…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0331-2015·2015-01-14

    Qualitest Recalls Acetaminophen and Codeine Oral Solution Due to Impurity

    Qualitest Pharmaceuticals is recalling specific lots of Acetaminophen and Codeine Phosphate Oral Solution because they failed impurity specifications for p-Aminophenol.

    Product
    ACETAMINOPHEN and CODEINE PHOSPHATE ORAL SOLUTION USP, 120 mg/12 mg per 5 mL, packaged in a) 4 oz. (120 mL) bottles, NDC 0603-9013-54, UPC 3 0603-9013-54 8 and b) ONE PINT (473 mL) bottles, NDC 0603-9013-58, UPC 3 0603-9013-58 6, Rx only, Manufactured for: QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0943-2015·2015-01-14

    Centurion Nerve Block Tray Recalled for Human Hair Contamination

    Centurion Medical Products is recalling 480 Nerve Block Trays due to a confirmed report of human hair embedded in a stopper.

    Product
    Nerve Block Tray (Nerve Block convenience kit)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0946-2015·2015-01-14

    Siemens Recalls Dimension Vista Myoglobin Calibrator Due to Positive Result Shift

    Siemens Healthcare Diagnostics is recalling Dimension Vista Myoglobin Calibrators because they may cause test results to shift up to 12% higher than expected.

    Product
    Dimension Vista Myoglobin Calibrator (MYO CAL), Lot 4FD085 Product usage: in vitro diagnostic product for the calibration of Myoglobin (MYO) method on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0938-2015·2015-01-14

    Stryker Orthobiologics Recalls Imbibe Bone Marrow Aspiration Needles

    Stryker Orthobiologics is recalling Imbibe Bone Marrow Aspiration Needles due to a potential breach in the inner or outer packaging pouches.

    Product
    Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle, Model Numbers: 2090-0027 Needle (bullet-tip), 11 gauge x 4 inch 2090-0028 Needle (bullet-tip), 11 gauge x 6 inch 2090-0029 Needle (bullet-tip), 8 gauge x 6 inch 2090-0047 Needle (bullet-tip), 8 gauge x 8 inch…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0332-2015·2015-01-14

    Par Pharmaceutical Recalls HydrALAZINE Tablets Due to Aluminum Particles

    Par Pharmaceutical is recalling one lot of HydrALAZINE Hydrochloride tablets because small aluminum particles were found in the product.

    Product
    HydrALAZINE Hydrochloride Tablets, USP 25 mg, 100 count bottle Rx only, Distributed by: Par Pharmaceutical Companies, Inc. Spring Valley, NY10977
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0937-2015·2015-01-14

    Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle Recall

    Stryker Orthobiologics is recalling Imbibe Aliquot Needle Bone Cement Needles due to potential breaches in the inner or outer packaging pouches.

    Product
    Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model Numbers: 2110-0505 Beveled Needle, 11 gauge x 4 inch 2110-0524 Beveled Needle, 11 gauge x 6 inch 2110-0506 Diamond Needle, 11 gauge x 4 inch 2110-0529 Diamond Needle, 11 gauge x 6 inch Intended Use: Can…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0907-2015·2015-01-14

    Spinal Elements Recalls Ti-Bond Marketing Literature Due to Misleading Claims

    Spinal Elements is recalling Ti-Bond marketing literature because the content regarding the Ti-Bond coating is unsubstantiated and misleading for spine applications.

    Product
    Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months non-operative treatment prior to being treated with this device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0932-2015·2015-01-14

    Baxter Amia Automated PD Systems Recalled for Battery Charging Error

    Baxter Healthcare is recalling 55 Amia Automated PD systems due to a battery charging error that prevents the device from functioning.

    Product
    Baxter Amia Automated PD systems are used in the treatment of adult renal failure patients to perform automated peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0333-2015·2015-01-14

    Akorn Recalls Triamcinolone Acetonide Lotion Due to Impurity Specification Failure

    Akorn, Inc. is recalling 3,937 bottles of Triamcinolone Acetonide Lotion USP, 0.025% because a known impurity exceeded specifications at the 12-month stability point.

    Product
    Triamcinolone Acetonide Lotion USP, 0.025% is supplied in the following size: 60 mL (NDC 61748-219-60).
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·15059·2015-01-13

    IKEA Recalls VYSSA Crib Mattresses Due to Entrapment Hazard

    IKEA is recalling VYSSA crib mattresses because they may create gaps larger than allowed by federal regulations, posing an entrapment risk to infants.

    Product
    VYSSA crib mattress
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·007-2015·2015-01-12

    US Foods Recalls Beef Fajita Strips Due to Undeclared Peanuts

    US Foods is recalling approximately 700 pounds of beef fajita strips because the product contains undeclared peanuts, a known allergen.

    Product
    US Foods Inc — New York Firm Recalls Beef Product Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V008000·2015-01-12

    Winnebago Recalls 2014-2015 Motorhomes Due to Tire Pressure Monitoring Defect

    Winnebago is recalling 2014-2015 Trend, Travato, and Itasca Viva motorhomes because the tire pressure monitoring system may fail to detect low tire pressure, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, TREND, ITASCA VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V006000·2015-01-09

    Ford Recalls 2015 Lincoln MKC Vehicles for Ignition Switch Defect

    Ford is recalling 2015 Lincoln MKC vehicles because the push-to-start button may be pressed accidentally, causing the engine to shut off and increasing crash risk.

    Product
    LINCOLN — LINCOLN MKC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V005000·2015-01-09

    Ford Recalls Vehicles Due to Fuel Pump Failure Risk

    Ford is recalling certain 2014-2015 vehicles because a defective fuel pump may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    FORD — FORD, LINCOLN FOCUS, ESCAPE, FIESTA, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15056·2015-01-08

    CoScentrix Expands Recall of DD Brand Candles Due to Fire Hazard

    CoScentrix is expanding its recall of DD brand candles sold at Hobby Lobby because the high flame can ignite the wax surface, posing a fire hazard.

    Product
    DD brand candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·15058·2015-01-08

    SKLZ Resistance Trainers Recalled Due to Risk of Severe Injury

    Pro Performance Sports is recalling SKLZ Recoil 360 Resistance Trainers because a weld can break, causing the cord to retract and injure users or partners.

    Product
    SKLZ Recoil 360™ All-Position Resistance Trainers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V003000·2015-01-08

    Lance Recalls 2015 Campers and Travel Trailers Due to Awning Bracket Defect

    Lance is recalling 2015 Slide-In Campers and Travel Trailers because awning mounting brackets may crack, causing the awning to fall and potentially injure people.

    Product
    LANCE — LANCE SLIDE-IN CAMPER, TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V004000·2015-01-08

    Thor Motor Coach Recalls 2015 Motorhomes Due to Awning Screw Defect

    Thor Motor Coach is recalling 154 model year 2015 motorhomes because defective awning screws could cause the awning to fall and injure people.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR CHATEAU CITATION, PALAZZO, FOUR WINDS 5000, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0756-2015·2015-01-07

    Safeway Select French Salted Caramel Ice Cream Recalled for Undeclared Peanut

    Safeway Inc is recalling Safeway Select French Salted Caramel Premium Ice Cream because peanut butter was used in the recipe but not listed on the label.

    Product
    Safeway Select French Salted Caramel (Fleur De Sel) Premium Ice Cream; 1.5 quart round paper carton with lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0329-2015·2015-01-07

    Ginseng Kianpi Pill Recalled for Undeclared FDA-Approved Drugs

    One and Zen is recalling Ginseng Kianpi Pill capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.

    Product
    GINSENG KIANPI PIL, 60 capsules, PRODUCT OF KWEILIN DRUG MANUFACTORY
    Category
    Drug
    Distribution
    Distributed nationwide