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.

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.

39551–39575 of 73919

  • SevereFDA (Drugs)·D-0488-2018·2018-02-28

    FDA Recalls Estradiol USP for Compounding Due to Stability Data Deficiencies

    American Pharmaceutical Ingredients LLC is recalling Estradiol USP (Micronized) (Yam) for prescription compounding due to a lack of stability data and controls to support assigned expiration dates.

    Product
    Estradiol USP (Micronized) (Yam) for prescription compounding, packaged in a) 1g (NDC 58597-8047-1); b) 5g (NDC 58597-8047-3); c) 10g (NDC 58597-8047-4); d) 25g (NDC 58597-8047-5); e) 100 g (NDC 58597-8047-6), RX only, packed by American Pharmaceutical Ingredients, LLC 6650…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0533-2018·2018-02-28

    FDA Recalls Vardenafil HCl for Prescription Compounding Due to Stability Data Gaps

    American Pharmaceutical Ingredients LLC is recalling Vardenafil HCl USP for prescription compounding due to a lack of stability data and controls supporting the assigned expiration dates.

    Product
    Vardenafil HCl USP (trihydrate) for prescription compounding, packaged in a) 5g (NDC 58597-8575-2); b) 100g (NDC 58597-8575-6);c) 500g (NDC 58597-8575-7); d) 1000g (NDC 58597-8575-8), RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0455-2018·2018-02-28

    Pharmedium Recalls Lidocaine HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Lidocaine HCl in 0.9% Sodium Chloride nationwide due to a lack of sterility assurance.

    Product
    Lidocaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0641-2018·2018-02-28

    Allen Medical Bow Frame Recalled Due to Potential Base Cracking

    Allen Medical Systems is recalling 161 Bow Frame Model A-70800 surgical platforms because the base may crack when patients are transferred onto the device.

    Product
    Allen Medical Bow Frame Model A-70800. Surgical platform used to position patients for lumbar spine procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2018·2018-02-28

    Pharmedium Recalls Dexamethasone Sodium Phosphate Infusions Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Dexamethasone Sodium Phosphate added to 0.9% Sodium Chloride in all strengths, doses, and packaging due to a lack of sterility assurance.

    Product
    Dexamethasone Sodium Phosphate added to 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0438-2018·2018-02-28

    Pharmedium Recalls Lidocaine HCl Due to Sterility Assurance Concerns

    Pharmedium Services, LLC is recalling all lots of Lidocaine HCl due to a lack of sterility assurance. The recall covers products distributed nationwide in the U.S.

    Product
    Lidocaine HCl in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0464-2018·2018-02-28

    Pharmedium Recalls Esmolol HCl Due to Lack of Sterility Assurance

    Pharmedium Services, LLC is recalling Esmolol HCl in all strengths and packaging due to a lack of sterility assurance.

    Product
    Esmolol HCl in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0434-2018·2018-02-28

    Pharmedium Recalls Midazolam HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Midazolam HCl in 0.9% Sodium Chloride due to a lack of sterility assurance.

    Product
    Midazolam HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0433-2018·2018-02-28

    Pharmedium Recalls Hydromorphone HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Hydromorphone HCl Injection due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    HYDROmorphone HCl Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0469-2018·2018-02-28

    Pharmedium Recalls Nicardipine HCl Infusions Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Nicardipine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance.

    Product
    Nicardipine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0451-2018·2018-02-28

    Pharmedium Recalls Ephedrine Sulfate Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Ephedrine Sulfate Injection due to a lack of sterility assurance.

    Product
    Ephedrine Sulfate Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0439-2018·2018-02-28

    Pharmedium Recalls Fentanyl Citrate Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Fentanyl Citrate in 0.9% Sodium Chloride due to a lack of sterility assurance.

    Product
    Fentanyl Citrate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0459-2018·2018-02-28

    Pharmedium Recalls All Nicardipine HCl Due to Sterility Assurance Issues

    Pharmedium Services, LLC is recalling all lots of Nicardipine HCl because the product lacks sterility assurance. The recall covers all strengths, doses, and packaging distributed nationwide.

    Product
    Nicardipine HCl in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0429-2018·2018-02-28

    Pharmedium Recalls Bupivacaine HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Bupivacaine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance. The recall covers 297 bags distributed nationwide.

    Product
    Bupivacaine HCl in 0.9% Sodium Chloride in all doses, all strengths, and packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0585-2018·2018-02-28

    Medtronic Recalls 951 Evera MRI ICDs Due to Therapy Prevention Risk

    Medtronic is recalling 951 Evera MRI ICDs and CRT-Ds because a defect may prevent high and low voltage therapy. Patients should contact their healthcare provider.

    Product
    Implantable Cardioverter Defibrillators (ICDs), Evera MRI. Labeled as the following: a. Evera MRI XT DR ICD DF1 (Product No. DDMB1D1); b. Evera MRI XT DR ICD DF4 (Product No. DDMB1D4); c. Evera MRI XT VR ICD DF4 (Product No. DVMB1D4); d. Evera MRI S DR ICD DF1…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0432-2018·2018-02-28

    Pharmedium Recalls Ephedrine Sulfate Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Ephedrine Sulfate in 0.9% Sodium Chloride nationwide due to a lack of sterility assurance.

    Product
    Ephedrine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0456-2018·2018-02-28

    Pharmedium Recalls Atropine Sulfate Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Atropine Sulfate Injection nationwide due to a lack of sterility assurance.

    Product
    Atropine Sulfate Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0431-2018·2018-02-28

    Pharmedium Recalls Fentanyl and Bupivacaine Injections Due to Sterility Concerns

    Pharmedium Services, LLC is recalling Fentanyl Citrate and Bupivacaine HCl injections due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.

    Product
    Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0449-2018·2018-02-28

    Pharmedium Recalls Midazolam HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Midazolam HCl Injection because of a lack of sterility assurance. The recall covers all strengths, doses, and packaging distributed nationwide.

    Product
    Midazolam HCl Injection in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0537-2018·2018-02-28

    FDA Recalls Methylcobalamin Due to Missing Stability Data

    American Pharmaceutical Ingredients LLC is recalling Methylcobalamin (Vitamin B12) for prescription compounding because the manufacturer lacked stability data to support the assigned expiration dates.

    Product
    Methylcobalamin (Vitamin B12) for prescription compounding, packaged in a) 500mg (NDC 58597-8142-1); b) 1g (NDC 58597-8056-2); c) 5g (NDC 58597-8056-3); d) 10g (NDC 58597-8056-4), e) 25 g (NDC 58597-8056-4); f) 100g (NDC 58597-8056-6), RX only, packed by American Pharmaceutical…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0586-2018·2018-02-28

    Medtronic Recalls Claria MRI CRT-Ds Due to Therapy Prevention Risk

    Medtronic is recalling 951 Claria MRI CRT-Ds because a defect may prevent the devices from delivering high or low voltage therapy.

    Product
    Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Claria MRI. Labeled as the following: a. Claria MRI CRT-D DF1 (Product No. DTMA1D1); b. Claria MRI Quad CRT-D DF4 (Product No. DTMA1QQ); EXPANSION: c. Claria MRI CRT-D DF4 (Product No. DTMA1D4); d.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0448-2018·2018-02-28

    Pharmedium Recalls Methadone HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Methadone HCl in 0.9% Sodium Chloride due to a lack of sterility assurance.

    Product
    Methadone HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0428-2018·2018-02-28

    Pharmedium Recalls Hydromorphone HCl Injection Due to Sterility Concerns

    Pharmedium Services, LLC is recalling all lots of Hydromorphone HCl in Sodium Chloride 0.9% due to a lack of sterility assurance.

    Product
    HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
    Category
    Drug
    Distribution
    Distributed nationwide