The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55201–55225 of 74005

  • ModerateFDA (Devices)·Z-1246-2015·2015-03-11

    DePuy Orthopaedics Recalls Partially Agglomerated SMARTSET GHV Bone Cement

    DePuy Orthopaedics is recalling one lot of SMARTSET GHV Gentamicin Bone Cement because it is partially agglomerated, which may cause surgical delays.

    Product
    SMARTSET GHV Gentamicin Bone Cement. A self-curing, radiopaque, polymethyl methacrylate based cement containing antibiotic. It is used for securing a metal or polymeric prosthesis to living bone in arthroplasty procedures. The bone cement has no intrinsic adhesive properties…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0397-2015·2015-03-11

    Qualitest Recalls Amlodipine Besylate Tablets Due to Oversized Size

    Qualitest Pharmaceuticals is recalling 2,808 bottles of Amlodipine Besylate tablets because one lot contains oversized tablets.

    Product
    AMLODIPINE BESYLATE TABLETS USP, 10 mg*, 1000 count bottles (NDC 0603-2110-32), Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1227-2015·2015-03-11

    Baxter Recalls Syringe Tip Caps for Missing Latex Symbol

    Baxter is recalling Self-Righting Syringe Tip Caps because the latex symbol is missing from the labels.

    Product
    Baxter, Self-Righting Syringe Tip Caps, Self-Righting DISCPAC Syringe Tip Caps. Product codes H93866100, H93869100, H93866025, H93867025, H93867100, H938671025, H938671100, H938673025, H938673100, H938674025, H938674100, H938676025, H938676100, H938677025, H938677100…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0404-2015·2015-03-11

    Pfizer Recalls Oxecta Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 139 bottles of Oxecta (oxycodone HCl) 7.5 mg tablets because they failed impurity and degradation specifications.

    Product
    Oxecta(TM) (oxycodone HCl) tablets, 7.5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-526-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0395-2015·2015-03-11

    Actavis Recalls Dextroamphetamine Sulfate Capsules for Dissolution Failures

    Actavis Elizabeth LLC is recalling 42 bottles of Dextroamphetamine Sulfate Extended-Release Capsules, 15 mg, because they failed dissolution specifications.

    Product
    DEXTROAMPHETAMINE SULFATE — DEXTROAMPHETAMINE SULFATE (DEXTROAMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1217-2015·2015-03-11

    Arjo Rotoprone Therapy System Recalled for Unapproved Medical Claims

    Arjo Hospital Equipment AB is recalling 226 Rotoprone Therapy Systems because their labeling and instructions for use contain unapproved medical claims.

    Product
    Rotoprone Therapy System. The Rotoprone Therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1231-2015·2015-03-11

    Siemens ADVIA Centaur Progesterone Kit Recalled for High Result Bias

    Siemens is recalling ADVIA Centaur Progesterone Kits due to high bias in results above 30 ng/mL. The recall affects 1,719 kits distributed worldwide.

    Product
    ADVIA Centaur Systems Progesterone Kit, (5-pack Ref); In Vitro Diagnostic Catalog number: 02177364; SMN: 10333111.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1229-2015·2015-03-11

    Siemens ADVIA Centaur Progesterone Kit Recall for High Bias in Results

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems Progesterone Kits because results above 30 ng/mL may show high bias.

    Product
    ADVIA Centaur Systems Progesterone Kit, (1 -pack) In Vitro Diagnostic; Catalog number: 02382928; SMN: 10310305.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1245-2015·2015-03-11

    Baxter AMIA v1.0 APD System Recall for Labeling Warning

    Baxter Healthcare is recalling 55 AMIA v1.0 APD Systems to add a warning about the risk of unintended increased intraperitoneal volume for vulnerable patients.

    Product
    AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy for pediatric and adult renal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1239-2015·2015-03-11

    CooperSurgical Pessary Kit Recalled for Incorrect Size Labeling

    CooperSurgical is recalling 95 units of Pessary Kit-CUBE#2 because the packaging label displays the incorrect size.

    Product
    CooperSurgical PESSARY KIT-CUBE#2, 1-3/8 in , 35 mm Part Number: MXKPEC02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0403-2015·2015-03-11

    Pfizer Recalls Oxecta Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 137 bottles of Oxecta (oxycodone HCl) 5 mg tablets because they failed impurity and degradation specifications.

    Product
    Oxecta(TM) (oxycodone HCl) tablets, 5 mg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc. Bristol, TN, NDC 60793-525-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1233-2015·2015-03-11

    Arrow FiberOptix Intra-Aortic Balloon Catheter Kit Recalled for Labeling Error

    Arrow International Inc. is recalling 165 units of FiberOptix Intra-Aortic Balloon Catheter Kits because the outer package label incorrectly identifies the product size.

    Product
    ARROW FiberOptix Intra-Aortic Balloon Catheter Kit, 40 cc 7.5 Fr Product Code: IAB-05840-LWS The Arrow IAB is utilized for intra-aortic balloon counter-pulsation therapy in the aorta, whereby balloon inflation, during diastole and deflation, during systole increases blood…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0402-2015·2015-03-11

    AvKARE Recalls Subpotent Quinapril Tablets Due to Low Drug Content

    AvKARE Inc. is voluntarily recalling 431 unit dose packs of Quinapril Tablets USP, 40 mg, because the medication was found to be subpotent.

    Product
    Quinapril Tablets USP, 40 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026869115, NDC 50268-691-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0401-2015·2015-03-11

    AvKARE Recalls Subpotent Quinapril Tablets Due to Low Dosage

    AvKARE Inc. is voluntarily recalling 214 unit dose packs of Quinapril 5 mg tablets nationwide because the medication is subpotent.

    Product
    Quinapril Tablets USP, 5 mg, Rx only, 50 tablets (5 X 10) unit dose pack, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, UPC 5026868815, NDC 50268-688-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V138000·2015-03-10

    Mercedes-Benz Recalls 2015 C300 and C400 for Fuel Pump Defect

    Mercedes-Benz is recalling 2015 C300 and C400 vehicles because the fuel delivery module may be improperly secured or have pinched wires, increasing the risk of fire or stalling.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C400, C300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V136000·2015-03-10

    Blue Bird Recalls School Buses Due to Improper Seat Belt Anchoring

    Blue Bird is recalling 2013-2016 All American and Vision school buses because incorrect fasteners may cause seat belts to be improperly anchored, increasing injury risk in crashes.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V137000·2015-03-10

    Mercedes-Benz Recalls CLS Models for Tail Light Visibility Defect

    Mercedes-Benz is recalling certain CLS 400, 550, and 63 models because LED tail lights may not illuminate on the sides, reducing rear visibility and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS550, CLS63, CLS400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15092·2015-03-10

    efco Gas Trimmers Recalled Due to Engine Muffler Fire Hazard

    Comet USA is recalling about 2,100 efco gas trimmers because the engine muffler can break during use, posing a fire hazard. Consumers should stop using the units and return them for a free replacement.

    Product
    efco Gas Trimmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V135000·2015-03-09

    Winnebago Recalls 2015 RVs Due to Door Opening Defect

    Winnebago is recalling 2015 ERA, View, and Itasca Navion vehicles because an incorrectly installed door component may make doors harder to open after a crash.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA VIEW, ERA, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V130000·2015-03-06

    Forest River Recalls 2015 XLR Nitro XLT31FQSL Recreational Vehicles

    Forest River is recalling 2015 XLR Nitro XLT31FQSL recreational vehicles because the fueling station hose may be too close to a fuel-burning appliance, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide