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.

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.

55526–55550 of 74005

  • SevereNHTSA·15V063000·2015-02-04

    Utility Recalls 2014-2015 Trailers Due to Brake Actuator Defect

    Utility Trailer Manufacturing Company is recalling 2014-2015 trailers because a brake actuator defect may cause overheating and fire.

    Product
    UTILITY — UTILITY, UTILITY TRAILER VS1RA, VS1DC, VS2DX, VS2RA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V064000·2015-02-04

    GM Recalls 2006-2007 Chevrolet and Pontiac Vehicles for Steering Defect

    General Motors is recalling specific 2006-2007 Chevrolet Malibu, Malibu Maxx, and Pontiac G6 vehicles because the electric power steering assist may suddenly fail, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, PONTIAC MALIBU, G6, MALIBU MAXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V065000·2015-02-04

    Morgan Olson Recalls 2014 Service Body Trucks for Lighting Defects

    Morgan Olson is recalling 11 model year 2014 Service Body trucks because rear identification and license plate lamps may be mounted incorrectly, reducing visibility.

    Product
    MORGAN OLSON — MORGAN OLSON SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V066000·2015-02-04

    Piaggio Recalls Vespa and Piaggio Motorcycles Due to Fuel Pump Defect

    Piaggio is recalling specific Vespa and Piaggio motorcycles because a defective fuel pump may cause the vehicle to stall or fail to restart, increasing crash risk.

    Product
    VESPA — VESPA, PIAGGIO LX 150, GTS SUPER 250, GTV 250, BV 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1011-2015·2015-02-04

    Philips BrightView MRI Systems Recalled for Unintended Movement

    Philips is recalling 1,064 BrightView MRI systems worldwide due to software issues causing unintended detector and gantry movement.

    Product
    BrightView model number: 882478 BrightView X model number: 882480 BrightView XCT model number: 882482 and 882454 Medical Device for imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1014-2015·2015-02-04

    Clinical Innovations Recalls Ebb Complete Tamponade System Due to Balloon Leak Risk

    Clinical Innovations, LLC is recalling 827 units of the Ebb Complete Tamponade System because of a potential for balloon leaks in lots manufactured since August 2014.

    Product
    Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2015·2015-02-04

    Sunrise Medical Recalls Six Quickie Q7 Adult Rigid Wheelchairs

    Sunrise Medical is recalling six Quickie Q7 Adult Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.

    Product
    Quickie Q7 Adult Rigid Wheelchair Model EIR4.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1023-2015·2015-02-04

    Beckman Coulter Lipase Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Lipase Assay kits because N-acetyl cysteine can cause falsely low results.

    Product
    Beckman Coulter, Lipase Assay, Catalog No. OSR6X30
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1012-2015·2015-02-04

    Aesculap Miethke Shunt System Accessories Recalled for Incorrect MR Safety Labeling

    Aesculap, Inc. is recalling Miethke Shunt System accessories because the shelf box labels incorrectly display an MR conditional symbol. The product is actually MR unsafe, and the correct information is only provided in the Instructions for Use.

    Product
    Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1024-2015·2015-02-04

    Beckman Coulter Uric Acid Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Uric Acid Assay kits because N-acetyl cysteine administration can cause falsely low test results.

    Product
    Beckman Coulter, Uric Acid Assay, Catalog No. OSR6X98
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0380-2015·2015-02-04

    Baxter Recalls Fluconazole Injection Bags Due to Seal Defects

    Baxter Healthcare is recalling 31,130 bags of Fluconazole Injection due to potential leaks from incomplete seals, which may compromise sterility.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1026-2015·2015-02-04

    Beckman Coulter Lactate Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Lactate Assay kits because N-acetyl cysteine (NAC) administration can cause falsely low test results.

    Product
    Beckman Coulter, Lactate Assay, Catalog No. OSR6X93
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2015·2015-02-04

    Beckman Coulter Cholesterol Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Cholesterol Assay kits because N-acetyl cysteine administration can cause falsely low results.

    Product
    Beckman Coulter, Cholesterol Assay, Catalog No. OSR6X16
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1027-2015·2015-02-04

    Siemens Syngo.plaza PACS Recalled for Potential Image Loss During System Crashes

    Siemens Medical Solutions is recalling 50 Syngo.plaza PACS systems because images may be lost if the system crashes before saving data to the hard disk.

    Product
    Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo.plaza also…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2015·2015-02-04

    Fresenius Kabi Recalls HEPFLUSH-10 Heparin Lock Flush Solution Due to pH Failure

    Fresenius Kabi is recalling HEPFLUSH-10 heparin lock flush solution because a specific lot failed pH specifications. The recall covers 69,725 units distributed nationwide.

    Product
    HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP units per 10 mL (10 USP units per mL), Single Dose Vial, Rx only -- Fresenius Kabi USA, LLC -- NDC 63323-017-10, Product Code 1710
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·028-2015·2015-02-04

    Krehbiels Specialty Meats Recalls Pork Bratwurst Due to Misbranding

    Krehbiels Specialty Meats is recalling approximately 29 pounds of pork bratwurst because the label failed to list all ingredients due to a printing error.

    Product
    Krehbiels Specialty Meats Inc — Recall Notification Report 028-2015 (Bratwurst)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1030-2015·2015-02-04

    Arrow Medical Kits Recalled for Incorrect Biopatch Dressing Size

    Arrow International Inc. is recalling specific medical kits because they were packaged with the incorrect size Biopatch Dressing. No risk to patients is anticipated.

    Product
    Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V057000·2015-02-03

    Mack Pinnacle Trucks Recalled for Brake Reservoir Defect

    Mack is recalling 2014-2015 Pinnacle trucks because a smaller air reservoir may increase stopping distance, raising crash risk.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V061000·2015-02-03

    Newmar Recalls 2014-2015 King Aire and Essex Vans for Brake Valve Defect

    Newmar is recalling 98 model year 2014-2015 King Aire and Essex vehicles because a damaged valve diaphragm may reduce air pressure, potentially compromising braking performance.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide