State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48451–48475 of 73995

CriticalFDA (Drugs)·D-0881-2016·2016-06-01
FDA Recalls Weight Loss Product Containing Undeclared Sibutramine and Phenolphthalein
Lucy's Weight Loss System is recalling Shorts on The Beach Golden Edition because it contains undeclared sibutramine and phenolphthalein.
Product
Shorts on The Beach Golden Edition by Pink Bikini, 800 mg, packaged in 30-count plastic bottle, Manufactured and Distributed by: Lucy's Weight Loss System, Arlington, Texas 76010
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0878-2016·2016-06-01
Smart Lipo Dietary Supplement Recalled for Undeclared Dangerous Ingredients
Centro Naturista is recalling Smart Lipo Dietary Supplement capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
Product
Smart Lipo Dietary Supplement capsules, 900 mg, packaged in 30-count plastic bottle, Distributed by: SmartLipo365, Arlington, TX 76011
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0869-2016·2016-06-01
Avastin Syringes Recalled for Bacterial Contamination
AmEx Pharmacy is recalling 45 Avastin syringes nationwide because testing revealed bacterial contamination.
Product
Avastin (Bevacizumab) 2 mg/0.08 mL syringe, Office Administration Only, AmEx Pharmacy, 1515 Elizabeth St Suite J, Melbourne, FL 32901.
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0879-2016·2016-06-01
Pink Bikini Strong Formula capsules recalled for undeclared ingredients
Lucy's Weight Loss System is recalling Pink Bikini Strong Formula capsules because they contain undeclared sibutramine and phenolphthalein and were marketed without an approved NDA/ANDA.
Product
Pink Bikini Strong Formula capsules, 750 mg, packaged in 30-count plastic bottle, Manufactured and Distributed by: Lucy's Weight Loss System, Arlington, Texas 76010
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0882-2016·2016-06-01
Pink Bikini capsules recalled for undeclared dangerous ingredients
Lucy's Weight Loss System is recalling Pink Bikini capsules because they contain undeclared Sibutramine, Phenolphthalein, and/or Diclofenac.
Product
Pink Bikini capsules, (all colors and all strengths), packaged in 30-count bottle, Manufactured and Distributed by: Lucy's Weight Loss System (dba Waisted With Lucy), Arlington, TX 76010
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0906-2016·2016-06-01
FDA Recalls Super Hard Capsules Marketed Without Approval
R Thomas Marketing, LLC is recalling Super Hard capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Super Hard, packaged in BIG BOX (20 small boxes / 6 capsules per box / 120 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0885-2016·2016-06-01
Herb Viagra Recalled for Lack of FDA Approval
R Thomas Marketing, LLC is recalling Herb Viagra because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Herb Viagra, packaged in Big Box (20 small boxes / 4 capsules per box / 80 capsules total), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0886-2016·2016-06-01
Real Skill Recalled for Marketing Without FDA Approval
R Thomas Marketing, LLC is recalling Real Skill capsules because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Real Skill, packaged in 20 small boxes / 4 capsules per box / 80 capsules total, Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1759-2016·2016-06-01
American Surgical Cotton Balls Recalled for Packaging Defect Compromising Sterility
American Surgical Company is recalling 34 boxes of strung cotton balls due to packaging defects that compromise sterility. The products were distributed worldwide.
Product
American Surgical Cotton Balls-Strung 1/8" Ref Number: 30-07 Product Usage: Neurosurgical and Nonneurosurgical Sponges
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0889-2016·2016-06-01
African Black Ant capsules recalled for lack of FDA approval
R Thomas Marketing, LLC is recalling African Black Ant capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
African Black Ant, packaged in 8 small boxes / 6 capsules per box / 48 capsules total, Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0892-2016·2016-06-01
FDA Recalls Unapproved Zhong Hua Niu Bian Capsules Nationwide
R Thomas Marketing, LLC is recalling Zhong Hua Niu Bian capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Zhong Hua Niu Bian, packaged in BIG BOX (6 small boxes / 6 capsules per box / 36 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0901-2016·2016-06-01
Man King capsules recalled for lack of FDA approval
R Thomas Marketing, LLC is recalling Man King capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Man King, packaged in BIG BOX (8 small boxes / 5 capsules per box / 40 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0867-2016·2016-06-01
Fresenius Kabi Recalls Octreotide Acetate Injection Due to Impurities
Fresenius Kabi USA is recalling Octreotide Acetate Injection vials because they failed impurities and degradation specifications.
Product
OCTREOTIDE ACETATE INJECTION, 50 mcg (base)/mL (0.05 mg/mL), 1 mL Single Dose Vial, Rx only, Manufactured by Fresenius Kabi USA, LLC, Schaumburg, IL 60173, NDC 63323-365-04
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0899-2016·2016-06-01
Plant Vigra Recalled for Lack of FDA Approval
R Thomas Marketing, LLC is recalling Plant Vigra because it was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Plant Vigra, packaged in BIG BOX / (18 cans / 6 capsules per can / 108 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0903-2016·2016-06-01
Night Man capsules recalled for lack of FDA approval
R Thomas Marketing, LLC is recalling Night Man capsules because the product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Night Man, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0896-2016·2016-06-01
FDA Recalls Black Storm Capsules Marketed Without Approval
R Thomas Marketing, LLC is recalling Black Storm capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Black Storm, packaged in SMALL BOX (6 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0891-2016·2016-06-01
Bull's Genital Recalled for Marketing Without FDA Approval
R Thomas Marketing, LLC is recalling Bull's Genital capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Bull's Genital, packaged in CASE (10 Cans / 10 capsules per can / 100 capsules),Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V382000·2016-06-01
Audi Recalls A4 and A6 Vehicles Due to Air Bag Inflator Rupture Risk
Volkswagen Group of America is recalling specific Audi A4 and A6 models because passenger air bag inflators may rupture during deployment, potentially causing serious injury or death.
Product
AUDI — AUDI A4, A6
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16E051000·2016-06-01
M.B. Sturgis Recalls Auto Changeover Propane Gas Regulators Due to Leak Risk
M.B. Sturgis is recalling specific propane gas regulators where a cracked window may allow gas to leak, increasing fire risk. Dealers will replace the parts free of charge.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1380-2016·2016-06-01
Sausage Maker Seasoning Recalled for Undeclared Milk Allergens
The Sausage Maker, Inc. is recalling Smoked Pepperoni seasoning because the Fermento ingredient contains undeclared whey protein and skim milk powder.
Product
THE SAUSAGE MAKER SEASONING Smoked Pepperoni under the following labels: 1) Net Wt 2 lbs, 2) Net Wt 25 lbs, 3) Smoked Pepperoni Kit w/Home Pak, 4) Smoked Pepperoni Salami Kit
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1379-2016·2016-06-01
Sausage Maker Seasoning Recalled for Undeclared Milk Allergens
The Sausage Maker, Inc. is recalling Goetburg Summer Sausage seasoning due to undeclared whey protein and skim milk powder.
Product
THE SAUSAGE MAKER SEASONING Goetburg Summer Sausage under the following labels: 1) Net Wt: 2 lbs.8 oz, 2) Goteborg Summer Sausage Kit
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0876-2016·2016-06-01
Akorn Recalls PerioRx Oral Rinse Due to Unknown Impurity
Akorn, Inc. is recalling PerioRx oral rinse because multiple batches failed impurity specifications. The product contains an unknown impurity of chlorhexidine gluconate.
Product
PerioRx (chlorhexidine gluconate), oral rinse, 0.12%, packaged in 16 fl. oz. (473 mL) PET bottle, Rx only, Manufactured for Discus Dental, LLC, Ontario, CA 91761, UPC 4235 020 91701
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0868-2016·2016-06-01
Teva Recalls Linezolid Injection Bags Due to Sterility Concerns
Teva North America is recalling 546 bags of Linezolid Injection due to potential leaking that compromises sterility.
Product
Linezolid Injection, 600 mg/300 mL Single use container bags (NDC 0703-9060-31), packaged in 10 x 300 mL Single Use Container bags per Box Pack (NDC 0703-9060-33), Rx only, Manufactured In Hungary By: Teva Pharmaceutical Works Ltd., Hungary, H-2100 Godollo, Tancsics M. ut 82…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0907-2016·2016-06-01
FDA Recalls Zhen Gong Fu for Lack of Approved New Drug Application
R Thomas Marketing, LLC is recalling Zhen Gong Fu capsules because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Zhen Gong Fu, packaged in BIG BOX (16 small boxes / 2 capsules per box / 32 capsules), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0884-2016·2016-06-01
FDA Recalls Black Ant Supplements Marketed Without Approval
The FDA is recalling Black Ant supplements distributed by R Thomas Marketing, LLC because they were marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA).
Product
Black Ant, packaged in Big Box (20 small boxes / 4 capsules per box / 80 capsules total), Distributed by: R Thomas Marketing, LLC, Bronx, NY 10467
Category
Drug
Distribution
Distributed nationwide