The Recall Desk

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.

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.

43151–43175 of 73919

  • ModerateFDA (Drugs)·D-0805-2017·2017-05-31

    Advanced Pharma Recalls Early TPN Neonatal Products for Latex Labeling

    Advanced Pharma Inc. is recalling Early TPN (Neonatal) products nationwide due to a labeling error regarding potential latex content.

    Product
    Early TPN (Neonatal) all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0817-2017·2017-05-31

    Advanced Pharma Recalls Cefazolin Due to Latex Labeling Deficiency

    Advanced Pharma Inc. is recalling all lots of Cefazolin because the product may contain latex but lacks appropriate labeling.

    Product
    Cefazolin all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0845-2017·2017-05-31

    Advanced Pharma Recalls Dexamethasone Sodium Phosphate for Latex Labeling

    Advanced Pharma Inc. is recalling Dexamethasone Sodium Phosphate because the product may contain latex but lacks proper labeling.

    Product
    Dexamethasone Sodium Phosphate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0804-2017·2017-05-31

    Advanced Pharma Recalls Standard Starter TPN Due to Latex Labeling

    Advanced Pharma Inc. is recalling Standard Starter TPN products because they may contain synthetic or natural latex without proper labeling.

    Product
    Standard Starter TPN all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0825-2017·2017-05-31

    Advanced Pharma Recalls Phenylephrine HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Phenylephrine HCl because the product may contain latex but lacks appropriate labeling.

    Product
    Phenylephrine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0808-2017·2017-05-31

    Advanced Pharma Recalls Sufentanil Citrate Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Sufentanil Citrate because the product may contain latex, which is not currently disclosed on the label.

    Product
    Sufentanil Citrate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0844-2017·2017-05-31

    Advanced Pharma Recalls Bumetanide Due to Latex Labeling Deficiency

    Advanced Pharma Inc. is recalling all strengths and dosage forms of Bumetanide because the product labeling fails to disclose that it may contain synthetic or natural latex.

    Product
    Bumetadine all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2153-2017·2017-05-31

    Innovasis Recalls Opteryx Variable Rescue Screws with Incorrect Size Engraving

    Innovasis, Inc. is recalling 21 Opteryx Variable Rescue Screws because they are engraved with an incorrect, larger size (16 instead of 14).

    Product
    Opteryx Variable Rescue Screw, Part #CP2214, UDI: *+M711CP22140/$$801716012*. Packaged in heat-sealed plastic bag. Product Usage: 4.5mm x 14mm Anterior Cervical Plate System Variable Rescue Screw. The Opteryx¿ Cervical Plate System is intended as a temporary fixation device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0842-2017·2017-05-31

    Advanced Pharma Recalls Famotidine HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Famotidine HCl because the product may contain latex but lacks proper labeling.

    Product
    Famotidine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0803-2017·2017-05-31

    Advanced Pharma Recalls TPN Neonatal Due to Latex Labeling

    Advanced Pharma Inc. is recalling TPN Neonatal products because they may contain latex but lack proper labeling.

    Product
    TPN Neonatal all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0848-2017·2017-05-31

    Magnesium Sulfate Recall for Potential Latex Content

    Advanced Pharma Inc. is recalling Magnesium Sulfate products due to potential latex content not clearly labeled.

    Product
    Magnesium Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0834-2017·2017-05-31

    Advanced Pharma Recalls Nicardipine HCl Due to Latex Labeling

    Advanced Pharma Inc. is recalling all lots of Nicardipine HCl because the product may contain latex but lacks appropriate labeling.

    Product
    Nicardipine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0830-2017·2017-05-31

    Advanced Pharma Recalls Amiodarone Due to Potential Latex Content

    Advanced Pharma Inc. is recalling all Amiodarone products due to a labeling issue regarding potential synthetic or natural latex content.

    Product
    Amiodarone all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0852-2017·2017-05-31

    Advanced Pharma Recalls Fentanyl Citrate with Ropivacaine HCl Due to Latex Labeling

    Advanced Pharma Inc. is recalling Fentanyl Citrate with Ropivacaine HCl because the product may contain latex and lacks appropriate labeling.

    Product
    Fentanyl Citrate with Ropivacaine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0810-2017·2017-05-31

    Advanced Pharma Recalls Hydromorphone HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Hydromorphone HCl because the product labeling does not properly disclose that it may contain synthetic or natural latex.

    Product
    Hydromorphone HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0828-2017·2017-05-31

    Advanced Pharma Recalls Epinephrine HCl Products Due to Latex Labeling

    Advanced Pharma Inc. is recalling all Epinephrine HCl products because they may contain latex but lack appropriate labeling.

    Product
    Epinephrine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0820-2017·2017-05-31

    Advanced Pharma Recalls Gentamicin Sulfate for Latex Labeling Defect

    Advanced Pharma Inc. is recalling all Gentamicin Sulfate products due to a labeling error regarding potential latex content.

    Product
    Gentamicin Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0843-2017·2017-05-31

    Advanced Pharma Recalls Ondansetron HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all strengths and dosage forms of Ondansetron HCl because the product labeling may not adequately disclose the presence of synthetic or natural latex.

    Product
    Ondansetron HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0839-2017·2017-05-31

    Advanced Pharma Recalls Neostigmine Methylsulfate Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all strengths and dosage forms of Neostigmine Methylsulfate because the product may contain latex without proper labeling.

    Product
    Neostigmine Methylsulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0836-2017·2017-05-31

    Advanced Pharma Recalls Labetalol HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling Labetalol HCl products because labels may not properly disclose the presence of synthetic or natural latex.

    Product
    Labetalol HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0819-2017·2017-05-31

    Advanced Pharma Recalls Penicillin G Potassium for Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Penicillin G Potassium because the product may contain latex but lacks appropriate labeling.

    Product
    Penicillin G Potassium all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0791-2017·2017-05-31

    Fagron Recalls Estriol Compounding Powder Due to Quality Assurance Deviations

    Fagron, Inc. is recalling Estriol for prescription compounding due to lack of quality assurance at the API manufacturer.

    Product
    Estriol, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-1392-1), b) 5 G bottle (NDC: 51552-1392-2), c) 25 G bottle (NDC: 51552-1392-3), d) 100 G bottle (NDC: 51552-1392-5), RX only, Distributed by Fagron, Inc. 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0861-2017·2017-05-31

    Mylan Recalls Norethindrone Acetate and Ethinyl Estradiol Tablets Due to Contamination

    Mylan Pharmaceuticals is recalling specific lots of oral contraceptive tablets due to chemical contamination from paint thinner vapors during facility repairs.

    Product
    NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL — NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0792-2017·2017-05-31

    Fagron Recalls Estrone Compounding Powder Due to Quality Assurance Deviations

    Fagron, Inc. is recalling Estrone for Prescription Compounding due to lack of quality assurance at the API manufacturer.

    Product
    Estrone, For Prescription Compounding, packaged in a) 1 G bottle (NDC: 51552-0445-1), b) 5 G bottle (NDC 51552-0445-2), c) 25 G bottle (NDC: 51552-0445-4), d) 100 G bottle (NDC: 51552-0445-5), RX only, Distributed by Fagron, Inc. 2400 Pilot Knob Rd, St. Paul, MN 55120 Tel.…
    Category
    Drug
    Distribution
    Distributed nationwide