State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40251–40275 of 73919

ModerateFDA (Drugs)·D-0170-2018·2018-01-17
KRS Global Biotechnology Recalls Chloramphenicol and Amphotericin Otic Powder
KRS Global Biotechnology is recalling 20 jars of Chloramphenicol and Amphotericin Otic Powder because the Beyond Use Date exceeds the expiration of at least one ingredient.
Product
Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0179-2018·2018-01-17
KRS Global Biotechnology Recalls Hydroquinone and Tretinoin Ointment Jars
KRS Global Biotechnology is recalling 30 jars of Hydroquinone 8%/Tretinoin 0.1% Topical Ointment because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Hydroquinone 8%/ Tretinoin 0.1% Topical Ointment packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0184-2018·2018-01-17
KRS Global Biotechnology Recalls Methylene Blue Injectable Vials for Labeling Errors
KRS Global Biotechnology is recalling 696 vials of Methylene Blue (PF) 10 mg/mL Injectable due to incorrect or missing lot and expiration dates.
Product
Methylene Blue (PF) 10 mg/mL (1%) Injectable Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0207-2018·2018-01-17
KRS Global Biotechnology Recalls 7-Keto DHEA Capsules Due to Labeling Error
KRS Global Biotechnology is recalling 7-Keto DHEA 25mg capsules because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
7-Keto DHEA 25mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0199-2018·2018-01-17
KRS Global Biotechnology Recalls Trimix #23F Due to Incorrect Expiration Date
KRS Global Biotechnology is recalling 94 vials of Trimix #23F because the product's expiration date exceeds the expiration date of at least one ingredient.
Product
Trimix #23F (Prostaglandin E1 6 mcg/ Papaverine HCl 17.8 mg/ Phentolamine Mesylate 0.6 mg/mL), For Intracavernous Use, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0201-2018·2018-01-17
KRS Global Biotechnology Recalls Ophthalmic Solution Due to Labeling Errors
KRS Global Biotechnology is recalling 297 droptainers of a multi-ingredient ophthalmic solution because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 2.5%/ 1%/ 0.5% Ophthalmic Solution, 3 mL Multi Dose Droptainer, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0161-2018·2018-01-17
KRS Global Biotechnology Recalls Anastrozole 0.5 mg Capsules for Labeling Errors
KRS Global Biotechnology is recalling 15,700 capsules of Anastrozole 0.5 mg due to incorrect or missing lot and expiration dates.
Product
Anastrozole 0.5 mg Capsules, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0168-2018·2018-01-17
FDA Recalls Bi-Est Cream Due to Expired Ingredient Dates
KRS Global Biotechnology is recalling 300 jars of Bi-Est Cream because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Bi-Est (Estriol/Estradiol) (80/20) + Progesterone 7.5 mg/200 mg Cream packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0206-2018·2018-01-17
FDA Recalls 7-Keto DHEA Capsules Due to Expired Ingredient
KRS Global Biotechnology is recalling 7-Keto DHEA 100 mg capsules because the product's expiration date exceeds the expiration date of at least one ingredient.
Product
7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0181-2018·2018-01-17
KRS Global Biotechnology Recalls Hydroxocobalamin Vials Due to Labeling Errors
KRS Global Biotechnology is recalling 596 vials of Hydroxocobalamin 1 mg/mL due to incorrect or missing lot and expiration dates.
Product
Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0196-2018·2018-01-17
KRS Global Biotechnology Recalls Sermorelin Acetate Vials Due to Labeling Errors
KRS Global Biotechnology is recalling 157 vials of Sermorelin Acetate/GHRP6 due to incorrect or missing lot and expiration dates.
Product
Sermorelin Acetate 3 mg/ GHRP6 3 mg, Lyophilized Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0209-2018·2018-01-17
Prinston Recalls Valsartan Tablets Due to Physical Specification Failures
Prinston Pharmaceutical Inc. is recalling 21,987 bottles of Valsartan 160 mg tablets because customer complaints confirmed the tablets were thicker and heavier than specifications.
Product
VALSARTAN — VALSARTAN (VALSARTAN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0603-2018·2018-01-17
Coconuthead Recalls CO YO Chocolate Coconut Yogurt Alternative Due to Container Bloating
Coconuthead LLC is recalling CO YO Coconut Yogurt Alternative CHOCOLATE because the containers are bloating. The product was distributed nationwide.
Product
CO YO Coconut Yogurt Alternative CHOCOLATE, 5.3 oz and 12 oz. plastic container, 6 packages per case. Store between 36 and 42 F. Manufactured by COCONUTHEAD, LLC, Albuquerque NM; Distributed by UNFI and KeHE
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0213-2018·2018-01-17
Dr. Reddy's Recalls Docetaxel Injection Vials Due to Seal Defects
Dr. Reddy's is recalling 1,051 vials of Docetaxel Injection USP due to defects in the vial seals that may allow the stopper to detach.
Product
DOCETAXEL — DOCETAXEL (DOCETAXEL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0164-2018·2018-01-17
KRS Global Biotechnology Recalls Topical Cream Due to Expired Ingredient
KRS Global Biotechnology is recalling 490 jars of Arginine/Lysine/Glutamine Topical Cream because the product's Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Arginine 150 mg/ Lysine HCl 50 mg/ Glutamine 200 mg/g Topical Cream packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0198-2018·2018-01-17
KRS Global Biotechnology Recalls Trimix #22F Due to Labeling Errors
KRS Global Biotechnology is recalling 235 vials of Trimix #22F because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
Trimix #22F (Prostaglandin E1 25 mcg/ Papaverine HCl 30 mg/ Phentolamine Mesylate 2 mg/mL), For Intracavernous Use, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0197-2018·2018-01-17
KRS Global Biotechnology Recalls Sincalide Vials Due to Labeling Errors
KRS Global Biotechnology is recalling 898 vials of Sincalide 5 mcg due to incorrect or missing lot and expiration dates.
Product
Sincalide 5 mcg Lyophilized Vials, For IV Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0191-2018·2018-01-17
KRS Global Biotechnology Recalls QUADMIX #18 Vials Due to Labeling Errors
KRS Global Biotechnology is recalling 129 vials of QUADMIX #18 because the Beyond Use Date exceeds the expiration date of at least one ingredient.
Product
QUADMIX #18, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0211-2018·2018-01-17
Akorn Recalls Gabapentin Oral Solution Due to Unapproved Manufacturer
Akorn Inc is recalling 4,885 bottles of Gabapentin Oral Solution because the product was released with an unapproved active ingredient manufacturer.
Product
Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only. Manufactured by: Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701. NDC: 50383-311-47
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0153-2018·2018-01-17
Enoxaparin Sodium Injection Recalled for Labeling Error on Declared Strength
Sanofi-Aventis is recalling Enoxaparin Sodium injections because a single syringe with a different strength was found in a carton labeled 120 mg/0.8 mL.
Product
ENOXAPARIN SODIUM — ENOXAPARIN SODIUM (ENOXAPARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
CriticalNHTSA·18V038000·2018-01-16
Mazda Recalls 2006 B-Series Trucks Due to Air Bag Inflator Defect
Mazda is recalling 2,205 model year 2006 B-Series trucks because the driver-side air bag inflator may explode upon deployment, posing a risk of serious injury or death.
Product
MAZDA — MAZDA B-SERIES TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18E004000·2018-01-16
Dorman Recalls A/C Bypass Pulley Brackets Due to Cracking Risk
Dorman is recalling specific A/C Bypass Pulley Brackets that may crack under certain loading conditions. A failure could cause the vehicle to lose power steering assist, increasing the risk of a crash.
Product
EQUIPMENT:APPLIANCE:AIR CONDITIONER recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·18V039000·2018-01-16
Mazda Recalls 2006 B-Series Trucks Due to Air Bag Inflator Defect
Mazda is recalling 2,205 model year 2006 B-Series trucks because the front air bag inflators may explode during deployment, posing a risk of serious injury or death.
Product
MAZDA — MAZDA B-SERIES TRUCK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·18V059000·2018-01-16
Liberty Recalls 2018 Little Guy Max Trailers Due to Jack Defect
Liberty is recalling 2018 Little Guy Max trailers because a cracked touch pad on the power tongue jack may allow water entry, causing the jack to operate unintentionally.
Product
LIBERTY — LIBERTY LITTLE GUY MAX
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18079·2018-01-16
Fujifilm Recalls Power Adapter Wall Plugs Due to Shock Hazard
Fujifilm is recalling power adapter wall plugs sold with certain digital cameras because they can crack or break, exposing live electrical contacts and posing a shock hazard.
Product
Power adapter wall plugs sold with Fujifilm digital cameras
Category
Consumer Product
Distribution
Distributed nationwide