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.

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.

60026–60050 of 74011

  • SevereFDA (Devices)·Z-0488-2014·2013-12-25

    Nephros SafeShower and SafeSpout Water Filters Recalled for Marketing Violations

    Nephros Inc. is recalling SafeShower and SafeSpout water filters because promotional materials marketed them as medical devices.

    Product
    1) Nephros SafeShower FH - 15 filters per box; item no. 70-0236 2) Nephros SafeShower HH -6 filters per box ; item no. 10-0237 Manufactured by : Nephros, Inc. 41 Grand Ave, River Edge, NJ 07661 Assembled at MEDICA 41036 Medolla, Italy The Nephros SafeSpout and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0748-2014·2013-12-25

    National Enzyme Recalls NWC Naturals Daily Cal Supplements Due to Chloramphenicol

    National Enzyme Co is recalling NWC Naturals Daily Cal dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    NWC Naturals, Daily Cal, packaged in 200-capsule bottles (SKU 53343). Manufactured exclusively for Natural Wellness Centers of American, Inc. Laguna Hills, CA.;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0751-2014·2013-12-25

    National Enzyme Recalls Phenol Assist Supplements Due to Chloramphenicol

    National Enzyme Co is recalling specific lots of Phenol Assist dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    Dietary Supplement packaged in the following configurations: (1) KIRKMAN Phenol Assist, packaged in 90-capsule bottles (SKU 52640). Manufactured exclusively for Kirkman, Lake Oswego, OR.; (2) 6379 Kirk Phenol Assist UNL, packaged in 90-capsule unlabeled bottles (SKU 53855)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-368-2014·2013-12-25

    Baxter Recalls Travasol Amino Acid Injection Due to Sterility Concerns

    Baxter Healthcare is recalling 14,622 bags of Travasol Amino Acid Injection because leaking containers prevent assurance of sterility.

    Product
    TRAVASOL — TRAVASOL (LEUCINE, PHENYLALANINE, LYSINE HYDROCHLORIDE, METHIONINE, ISOLEUCINE, VALINE, HISTIDINE, THREONINE, TRYPTOPHAN, ALANINE, GLYCINE, ARGININE, PROLINE, TYROSINE, SERINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0778-2014·2013-12-25

    National Enzyme Recalls Bulk DPPIV Digest Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk DPPIV digest powder that may contain chloramphenicol above 0.3 ppb.

    Product
    Bulk A216 MRM DPPIV DIGEST BULK powder (SKU 83217), packaged in varying quantities within poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0803-2014·2013-12-25

    National Enzyme Co Recalls Dietary Supplements for Chloramphenicol Contamination

    National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Carbo Converter-I powder, packaged 25 gram bottles (SKU 54663). Firm name on the label is National Enzyme Company, Forsyth, MO; (2) C560 NEC Carb Converter Blen packaged in unlabeled, 25 gram bottles.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0766-2014·2013-12-25

    National Enzyme Recalls DigestEasy Supplements Due to Chloramphenicol Contamination

    National Enzyme Co is recalling DigestEasy enzyme supplements because a raw material may contain chloramphenicol above the allowed limit.

    Product
    DigestEasy, Hypoallergenic Enzyme Supplement, packaged in 60-capsule bottles (SKU 53557). Firm name on the label is Master The Body, Joliet, IL
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0764-2014·2013-12-25

    National Enzyme Recalls Bulk Candidachlorel Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk Candidachlorel powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 9414 PROTHERA CANDIDACHLOREL powder, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83056);
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0753-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements for Potential Chloramphenicol Contamination

    National Enzyme Co is recalling specific lots of DigestiveBlend powder dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Dietary Supplements packaged in the following configurations: (1) Bulk 6916 Shanghai DigestiveBlend powder, packaged in varying quantities in poly bags within fiber drums (SKU 83274); (2) Bulk 6916 WEDAR DIGESTIVEBLEND powder, packaged in varying quantities in poly bags…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0485-2014·2013-12-25

    Abbott FreeStyle Blood Glucose Test Strips Recalled for Erroneous Results

    Abbott Diabetes Care is recalling specific lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips because they may produce erroneously low blood glucose readings.

    Product
    FreeStyle Blood Glucose Test Strips; For in vitro diagnostic testing. 50 count UPC 6 99073 12050 2; Freestyle Blood Glucose Test Strips; for Institutional Use only 50 count: UPC 6 99073 70792 5 Manufactured by Abbott Diabetes Care Inc. Alameda, CA. The FreeStyle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0738-2014·2013-12-25

    National Enzyme Recalls Bulk Digest Powder Due to Chloramphenicol

    National Enzyme Co is recalling 3989 Bulk TPP TEC DIGEST powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    3989 Bulk TPP TEC DIGEST powder, Transformation Enzyme Corporat, packaged in varying quantities in poly bags within corrugated containers. SKU 81814
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0472-2014·2013-12-25

    GE Healthcare Recalls Multi Absorber Original Devices Due to Air Leakage

    GE Healthcare is recalling Multi Absorber Original, Disposable devices due to a potential safety issue involving air leakage associated with the CO2 Multi Absorber.

    Product
    Multi Absorber Original, Disposable M1173310 Multi Absorber Original, Disposable, package of 6 pcs, GE Healthcare Finland Oy Made in US Rx Only The GE Healthcare Multi Absorber Original, Disposable is a disposable product intended for use with the GE Healthcare Advanced…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0788-2014·2013-12-25

    National Enzyme Recalls TriEnza Powder Due to Potential Chloramphenicol Contamination

    National Enzyme Co is recalling TriEnza Powder dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    TriEnza Powder with DPP IV Activity, packaged 105 gram bottles (SKU 54045). Firm name on the label is Houston Nutraceuticals, Inc., (HNI), Siloam Springs, AR;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0487-2014·2013-12-25

    Nephros SafeSpout Water Filters Recalled for Improper Medical Device Marketing

    Nephros Inc. is recalling SafeSpout water filters because promotional materials made claims that marketed the non-medical products as medical devices.

    Product
    Nephros SafeSpout Manufacturer: Nephros Inc. 41 Grand Avenue, River Edge, NJ 07661 Assembled at : MEDICA 41036 Medolla, Italy Filters are packaged in a Tyvek pouch and then placed inside a cardboard box. 15 filters per box The Nephros SafeSpout and SafeShower are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0737-2014·2013-12-25

    National Enzyme Recalls CarbohydrEnz Supplements Due to Chloramphenicol

    National Enzyme Co is recalling CarbohydrEnz dietary supplements because a raw material may contain chloramphenicol above 0.3 ppb.

    Product
    Advanced Formula, CarbohydrEnz, packaged in 60-(SKU 52083) capsule bottles. The firm name on the label is Enzymes, Inc., Parkville, MO
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0540-2014·2013-12-25

    Smiths Medical Recalls Medfusion 4000 Syringe Infusion Pumps for Electrical Shorting

    Smiths Medical is recalling Medfusion 4000 Syringe Infusion Pumps because conductive fluids entering the AC power receptacle can cause electrical shorting, sparking, or flames.

    Product
    Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion Pumps are designed for use in care areas for the administration of fluids requiring precisely controlled infusion rates. These pumps are indicated for use by healthcare professionals in the delivery of IV…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0794-2014·2013-12-25

    National Enzyme Recalls Legume Digest 2.0 Due to Chloramphenicol

    National Enzyme Co is recalling IMTWellnes Legume Digest 2.0 dietary supplements because they may contain chloramphenicol above 0.3 ppb.

    Product
    IMTWellnes, Legume Digest 2.0, packaged 120-capsule bottles (SKU 54179). Firm name on the label is ANAT, LLC, Bloomfield, CT;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0486-2014·2013-12-25

    Abbott FreeStyle Blood Glucose Test Strips Recalled for Erroneous Low Results

    Abbott Diabetes Care is recalling certain lots of FreeStyle and FreeStyle Lite Blood Glucose Test Strips because they may produce erroneously low blood glucose readings.

    Product
    FreeStyle Lite Blood Glucose Test Strips; For in vitro diagnostic testing. 50 count; 100 count Product of Ireland; UPC 6 99073 70819 9; - 50 count UPC 6 99073 70822 9 - 50 count UPC 6 99073 71026 0 - 50 count UPC 6 99073 70827 4 - 100 count Manufactured by Abbott…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0781-2014·2013-12-25

    National Enzyme Recalls Pet Di Powder Due to Chloramphenicol Contamination

    National Enzyme Co is recalling Bulk A776 Healthline Nutri Pet Di powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A776 Healthline Nutri Pet Di powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83287);
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0490-2014·2013-12-25

    Nephros Dual Stage Ultra Filter Brochure Recalled for Misleading Medical Claims

    Nephros Inc is recalling brochures for its Dual Stage Ultra Filter because the materials promoted the product as a medical device.

    Product
    Nephros Dual Stage Ultra Filter (DSU) Brochure Document 60-3003 Revisions: 0, 1, 2 Product Usage: A disposable point of use water ultrafilter that delivers microbiologically pure water for washing and drinking.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0782-2014·2013-12-25

    National Enzyme Recalls Digestive Bul Powder for Chloramphenicol Contamination

    National Enzyme Co is recalling Bulk A957 Nutra Med Digestive Bul powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk A957 Nutra Med Digestive Bul powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83318);
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2014·2013-12-25

    Senor Murphy Candymaker Recalls Multiple Candies Due to Undeclared Allergens

    Senor Murphy Candymaker is recalling eight types of candy products because they contain undeclared allergens.

    Product
    Senor Murphy Santa Fe Candymaker Chili Peanut Brittle , 4 oz and 1 lb. Handmade with sugar, corn syrup, peanuts, butter, soda, chile, and salt.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0539-2014·2013-12-25

    Baxter ABACUS TPN Calculation Software Recalled for Data Corruption Risk

    Baxter is voluntarily correcting ABACUS TPN software versions 2.0-3.0 because data corruption could cause patients to receive another patient's TPN order.

    Product
    ABACUS TPN Calculation Software, Baxa: 8300-0045 ABACUS CE (Calculator Edition), 8300-0046 ABACUS SE (Single-Workstation Edition), 8300-0047 ABACUS ME (Multi-Workstation Edition) ABACUS is a Windows¿ - based order entry TPN software application for comprehensive calculations…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0538-2014·2013-12-25

    Remel Inc. Recalls Streptex Latex D Reagent for False Negative Results

    Remel Inc. is recalling 109 kits of Streptex Latex D reagent because the product may produce weak or false negative test results for streptococcal group D.

    Product
    Streptex* Latex D, Ref R30950901 ZL54, IVD, Latex reagent for streptococcal group D, 50 tests per box. The firm name on the label is Remel Inc., Lenexa, KS, Manufactured by Remel Europe Ltd., Dartford Kent, UK. Streptex is a rapid latex test system for use in the qualitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0524-2014·2013-12-25

    GE Recalls InstaTrak and ENTrak Computer-Assisted Navigation Systems

    GE OEC Medical Systems is recalling InstaTrak and ENTrak navigation systems due to potential safety issues.

    Product
    InstaTrak¿ 3500 Plus, ENTrakTM Plus, InstaTrak¿ 3500, ENTrakTM Computer-Assisted Navigation Systems (USA),
    Category
    Medical Device
    Distribution
    Distributed nationwide