The Recall Desk

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.

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.

50776–50800 of 73995

  • SevereFDA (Drugs)·D-0440-2016·2015-12-09

    Western Drug Recalls 18 Containers of Omnitrope Injection Kits

    Western Drug is recalling 18 containers of Omnitrope 17.4U/10mL Injection Kits due to a lack of assurance of sterility. The product was distributed nationwide in eight states.

    Product
    Omnitrope 17.4U/10mL Inj-Kit, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V826000·2015-12-09

    Jeep Cherokee Recall: Power Liftgate Module Fire Risk

    Chrysler is recalling 2015-2016 Jeep Cherokees with power liftgates because water leaks into the control module, creating a fire risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0464-2016·2015-12-09

    Western Drug Recalls Tri-Mix ED Injection Due to Sterility Concerns

    Western Drug is recalling 68 containers of Tri-Mix ED Injection because the product lacks assurance of sterility. The recall covers distribution in eight U.S. states.

    Product
    Tri-Mix ED Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0505-2016·2015-12-09

    Methyfolate Capsules Recalled for Potential Penicillin Cross Contamination

    Life Science Pharmacy Inc. is recalling Methyfolate Capsules due to potential penicillin cross contamination. The recall is nationwide and affects all lots.

    Product
    METHYLFOLATE Capsules, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0506-2016·2015-12-09

    Methyfolate Injection Recalled for Potential Penicillin Contamination

    Life Science Pharmacy Inc. is recalling Methyfolate Injection due to potential penicillin cross-contamination. The recall covers all lots distributed nationwide.

    Product
    METHYLFOLATE Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0474-2016·2015-12-09

    Western Drug Recalls Sodium Hydroxide 10% Injection Due to Sterility Concerns

    Western Drug is recalling Sodium Hydroxide 10% Injection because the company cannot ensure the product is sterile. The recall covers all lots distributed nationwide.

    Product
    Sodium Hydroxide 10% Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0354-2016·2015-12-09

    Philips Xper Vascular System Monitor Ceiling Suspension Recall

    Philips Medical Systems is recalling 22 Allura Xper vascular systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0460-2016·2015-12-09

    Western Drug Recalls Tev-Tropin Injection Due to Sterility Concerns

    Western Drug is recalling six containers of Tev-Tropin (Somatropin) Injection due to a lack of assurance of sterility. The product was distributed nationwide in eight states.

    Product
    Tev-Tropin (Somatropin) Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0488-2016·2015-12-09

    Life Science Pharmacy Recalls Hydroxocobalamin Injection Due to Penicillin Contamination

    Life Science Pharmacy Inc. is recalling Hydroxocobalamin Injection due to potential penicillin cross-contamination. The recall covers all lot numbers and expiration dates distributed nationwide.

    Product
    HYDROXOCOBALAMIN Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0507-2016·2015-12-09

    Life Science Pharmacy Recalls HCG Injections Due to Penicillin Contamination

    Life Science Pharmacy Inc. is recalling Human Chorionic Gonadotropin (HCG) injections nationwide due to potential penicillin cross-contamination.

    Product
    HUMAN CHORIONIC GONADOTROPIC (HCG) Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0442-2016·2015-12-09

    Western Drug Recalls Podophyllum 40% Topical Due to Sterility Concerns

    Western Drug is recalling Podophyllum 40% Topical because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Podophyllum 40% Topical, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0439-2016·2015-12-09

    Western Drug Recalls Novarel HCG Vials Due to Sterility Concerns

    Western Drug is recalling Novarel HCG 10000U/Vial prescription vials nationwide due to a lack of assurance of sterility.

    Product
    Novarel "HCG" 10000U/Vial, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V829000·2015-12-09

    Newmar Recalls Motorhomes Due to Steering Gear Bracket Crack Risk

    Newmar is recalling specific model year 1997-2005 motorhomes because a steering gear mounting bracket may crack, potentially causing a loss of steering ability.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, KOUNTRY AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0429-2016·2015-12-09

    Western Drug Recalls Heparin Injection Due to Sterility Concerns

    Western Drug is recalling Heparin 1000 Unit/mL Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.

    Product
    Heparin 1000 Unit/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0435-2016·2015-12-09

    Western Drug Recalls Magnesium Chloride Injection Due to Sterility Concerns

    Western Drug is recalling Magnesium Chloride Injection because the product lacks assurance of sterility. The recall covers two containers distributed nationwide.

    Product
    Magnesium Chloride Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0403-2016·2015-12-09

    Western Drug Recalls Depo-Testadiol Injection Due to Sterility Concerns

    Western Drug is recalling Depo-Testadiol 10/5mg/mL Injection because the product lacks assurance of sterility. The recall affects four containers distributed nationwide.

    Product
    Depo-Testadiol 10/5mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0401-2016·2015-12-09

    Western Drug Recalls Cyclosporine Eye Drops Due to Sterility Concerns

    Western Drug Inc. is recalling four containers of Cyclosporine 1% Opth Sol because the product lacks assurance of sterility. The recall covers distribution in eight US states.

    Product
    Cyclosporine 1% Opth Sol, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0484-2016·2015-12-09

    Western Drug Recalls Salicylic Acid Injections Due to Sterility Concerns

    Western Drug is recalling Salicylic Acid Injections because the company cannot ensure the product is sterile. The recall covers all lots distributed nationwide.

    Product
    Salicylic Acid Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0422-2016·2015-12-09

    Western Drug Recalls Calcium EDTA Injection Due to Sterility Concerns

    Western Drug is recalling Calcium EDTA 300mg/mL Injection because the product lacks assurance of sterility. The recall affects two containers distributed nationwide.

    Product
    Calcium EDTA 300mg/mL Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0443-2016·2015-12-09

    Western Drug Recalls Potassium Chloride Injection Due to Sterility Concerns

    Western Drug is recalling two containers of Potassium Chloride 40 mEq/mL Injection because the product lacks assurance of sterility.

    Product
    Potassium Chloride 40 mEq/mL Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0448-2016·2015-12-09

    Western Drug Recalls Quad Mix Injections Due to Sterility Concerns

    Western Drug is recalling 15 containers of Quad Mix Inj because the company cannot ensure the product is sterile.

    Product
    Quad Mix Inj, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0420-2016·2015-12-09

    Western Drug Recalls Benadryl Injection Due to Sterility Concerns

    Western Drug is recalling Benadryl 50mg/2mL Pres-Free Injection because the product lacks assurance of sterility. The recall covers all lots distributed nationwide.

    Product
    Benadryl 50mg/2mL Pres-Free Injection, Rx, Western Drug Inc. 106 E. Main Street, Springerville, Arizona 85938
    Category
    Drug
    Distribution
    Distributed nationwide