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.

60001–60025 of 74011

  • LowFDA (Drugs)·D-382-2014·2014-01-01

    Teva Recalls Qnasl Nasal Aerosol Due to Potential Clogged Stem Valves

    Teva Pharmaceuticals USA is recalling Qnasl Nasal Aerosol units because some may have clogged stem valves, potentially affecting delivery.

    Product
    Qnasl (beclomethasone dipropionate) Nasal Aerosol, 80 mcg per spray, 120 metered sprays, 8.7 g inhaler, Rx only, Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Delivery Systems, Northridge, CA 91324, NDC 59310-210-12, UPC 3 59310 21012 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-389-2014·2014-01-01

    Hi-Tech Pharmacal Recalls Acyclovir Oral Suspension for Stability Failures

    Hi-Tech Pharmacal is recalling Acyclovir Oral Suspension because the product's viscosity and pH levels fell below required specifications.

    Product
    Acyclovir Oral Suspension, USP 200 mg/5 mL, Net Wt. 16 fl oz (473 mL), Rx only, Hi-Tech Pharmacal Co, Inc. Amityville, NY 11701. NDC 50383-810-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V651000·2013-12-30

    Oshkosh Recalls 2013 S-Series Trucks Due to Brake Pedal Bracket Defect

    Oshkosh is recalling 2013 S-Series ready mixed concrete trucks because missing lock washers may allow the brake pedal bracket to loosen, reducing braking capability.

    Product
    OSHKOSH — OSHKOSH S-SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14073·2013-12-30

    Specialized Recalls 2012 Source Bicycles Due to Front Hub Fall Hazard

    Specialized is recalling about 173 2012 Source Eleven and Source Expert Disc bicycles because front hub set screws can loosen, causing the front wheel to stop turning and posing a fall hazard.

    Product
    2012 Source Eleven and Source Expert Disc bicycles with Supernova Switchable Dynamo Front Hubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14074·2013-12-30

    Cabrinha H2 Kiteboarding Binding Recalled Due to Injury Risk

    Cabrinha is recalling H2 Hydra Series kiteboarding bindings because they can detach from the base, causing loss of control and injury.

    Product
    Cabrinha H2 Hydra Series Binding
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V647000·2013-12-26

    Bay Bridge Manufacturing Recalls Cargo Vans and Trailers with Jamming Door Locks

    Bay Bridge Manufacturing is recalling 2006-2013 cargo vans and trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    BAY BRIDGE MFG — BAY BRIDGE MFG FRP UNIT, CLASSIC UNIT, SHEET AND POST UNIT, SHEET & POST UNIT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V650000·2013-12-26

    Prevost Recalls 682 Motorhomes and Coaches for Windshield Wiper Motor Defect

    Prevost is recalling 682 model year 2012-2014 motorhomes and coaches because a windshield wiper motor housing may crack, causing loss of wiper function and reduced visibility.

    Product
    PREVOST — PREVOST H3-45, H3-45 VIP, X3-45, X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-370-2014·2013-12-25

    Zi Xiu Tang Ultimate Formula Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Ultimate Formula capsules because they contain undeclared sibutramine, an ingredient removed from the market for safety reasons.

    Product
    Ultimate Formula, Net Wt. 250 mg, 48 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 7 9357304140 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-371-2014·2013-12-25

    Quick Thin capsules recalled for containing unapproved drugs

    Bethel Nutritional Consulting is recalling Quick Thin capsules because FDA analysis detected unapproved drugs sibutramine and phenolphthalein.

    Product
    Quick Thin (citrus aurantium extract, sweet potato fiber, cyamopsis gum powder, alfalfa, mulberry leaf, guarana, spirulina) capsules, 400 mg, 30-count bottle, Distributed by: Bethel, Inc., Tel: (212) 568-5330.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-381-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 119,600 vials of Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-369-2014·2013-12-25

    Bee Pollen Capsules Recalled for Undeclared Sibutramine

    Zi Xiu Tang Success, LLC is recalling Classic Zi Xiu Tang Bee Pollen Capsules because they contain undeclared sibutramine, an unapproved active ingredient.

    Product
    Classic Zi Xiu Tang, Bee Pollen Capsule, Net Wt. 250 mg x 60 capsules per bottle, Distributed by: Zi Xiu Tang Success, LLC., Trexlertown, PA 18087, UPC 6 937000 700019
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-380-2014·2013-12-25

    Hospira Recalls Bupivacaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 118,100 vials of 0.25% Bupivacaine Hydrochloride Injection due to the presence of visible particulate matter.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-375-2014·2013-12-25

    Altaire Recalls Carboxymethylcellulose Sodium Eye Drops Due to Non-Sterility

    Altaire Pharmaceuticals is recalling specific lots of Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution because the preservative may not be effective through expiry, posing a non-sterility risk.

    Product
    Carboxymethylcellulose Sodium 0.5% Ophthalmic Solution, 1 FL OZ (30 mL) bottle, sold under the following labels: (a) CVS pharmacy brand LUBRICANT EYE DROPS FOR MILD TO MODERATE DRY EYE, Distributed by CVS Pharmacy, Inc., Woonsocket, RI 02895, UPC 0 50428 053357 7 and UPC 0 50428…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0812-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive B Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk Digestive B powder that may contain chloramphenicol above 0.3 ppb. The product was distributed domestically and internationally.

    Product
    Bulk D008 Glykon Tech Digestive B powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83453)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0767-2014·2013-12-25

    National Enzyme Recalls GLUTENEZYME Capsules Due to Chloramphenicol Contamination

    National Enzyme Co is recalling GLUTENEZYME capsules because the raw material may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 9730 BIOSANLABS GLUTENEZYME capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92103).
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0750-2014·2013-12-25

    National Enzyme Recalls WellZymes Supplements Due to Chloramphenicol Contamination

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

    Product
    Dietary Supplement packaged in the following configurations: (1) WELLZYMES, Carbohydrate Digestion, Enzyme Supplement packaged in 90-capsule bottles (SKU 52644). Manufactured exclusively for enzymes, inc., Parkville, MO.; (2) 6306 WellZymes CarboDigest U, packaged in…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0760-2014·2013-12-25

    National Enzyme Recalls Pro-3-Zyme Supplements Due to Chloramphenicol

    National Enzyme Co is recalling 598 bottles of Northern Nutrition Pro-3-Zyme dietary supplements because they may contain chloramphenicol.

    Product
    Northern Nutrition, Pro-3-Zyme, packaged in 180-capsule bottles (SKU 53373). Firm name on the label is Northern Nutrition, LLC, Shipshewana, IN;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0808-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Blend Powder Due to Chloramphenicol

    National Enzyme Co is recalling bulk Global Digestive Blend powder because it may contain chloramphenicol above the 0.3 ppb limit.

    Product
    Bulk C676 BnG Global Digestive Blend powder, packaged in varying quantities within poly bags within corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 83430)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0754-2014·2013-12-25

    National Enzyme Recalls Dietary Supplements Due to Potential Chloramphenicol Contamination

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

    Product
    Dietary Supplements packaged in the following configurations: (1) 7 Lights, FULL SPECTRUM ENZYMES, packaged in 90 capsule bottles (SKU 52785). Firm name on the label is 7 Lights, Black Mountain, NC; (2) 6926 Crusador TempleBuilders, packaged in unlabeled 90 capsule bottles…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-372-2014·2013-12-25

    Bethel Advance capsules recalled for unapproved drug ingredients

    Bethel Nutritional Consulting is recalling Bethel Advance capsules because FDA analysis detected unapproved drug ingredients, including phenolphthalein and sibutramine.

    Product
    Bethel Advance (bitter orange, mulberry leaf, cassia seed extract, jobstear seed, spirulina, starch, kola nut) capsules, 400 mg, 30-count bottles, Distributed by: Bethel, Inc., Tel: (212) 568-5330, UPC 1 60126 41750 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0775-2014·2013-12-25

    National Enzyme Recalls Bulk Digestive Powder Due to Chloramphenicol

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

    Product
    Bulk A164 NUTRACHOICE DIGESTIVEBL powder (SKU 83196), 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-0761-2014·2013-12-25

    National Enzyme Recalls YogiHouse Digestive Bul Powder for Chloramphenicol

    National Enzyme Co is recalling YogiHouse Digestive Bul powder because it may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 9245 YOGIHOUSE DIGESTIVE BUL powder, packaged in poly bags within corrugated containers (SKU 82993);
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-367-2014·2013-12-25

    West-Ward Recalls Carisoprodol Tablets Due to Foreign Substance Presence

    West-Ward Pharmaceutical Corp. is recalling 20,534 bottles of Carisoprodol Tablets, USP 350 mg, because heavy metals and inactive components were visually observed during routine stability testing.

    Product
    Carisoprodol Tablets, USP 350 mg, Rx Only, 1000 tablets. Dist by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724. Mfd by: Shasun Chemicals and Drugs Limited, Unit II, R. S. Na 32, 33, 743 PIMS Rd, Periyakalepet, Pondicherry. 605014 INDIA. NDC 0143-9749-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0763-2014·2013-12-25

    National Enzyme Recalls Digestenzyl Capsules Due to Chloramphenicol Contamination

    National Enzyme Co is recalling bulk Digestenzyl capsules because they may contain chloramphenicol levels exceeding 0.3 ppb.

    Product
    Bulk 9399 OceanwideUSA DIGESTENZY capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92033);
    Category
    Food
    Distribution
    Distributed nationwide