The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53001–53025 of 74002

  • ModerateFDA (Devices)·Z-2070-2015·2015-07-22

    Exactech Recalls Four Ambassador Cervical Plate Systems

    Exactech, Inc. is recalling four Ambassador Cervical Plate Systems that were shipped to a single consignee in Florida before final inspection was completed.

    Product
    Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical Place System is intended for anterior cervical fixation (C2-T1) for the following: degenerative disc disease (DDD) (defined as neck pain of discogenic origin with degeration of the disc confirmed by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1242-2015·2015-07-22

    Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization

    Hospira Inc. is recalling specific lots of Ketorolac Tromethamine Injection due to the presence of crystals identified as the calcium salt of Ketorolac.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2071-2015·2015-07-22

    Exactech Single Barrel Drill Guides Recalled for Incomplete Final Inspection

    Exactech, Inc. is recalling two Single Barrel Drill Guides shipped to a single consignee in Florida before final inspection was completed.

    Product
    Exactech Single Barrel Drill Guides The Single Barrel Drill Guide is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2075-2015·2015-07-22

    Musculoskeletal Transplant Foundation Recalls Allofix Insertion Kits Due to Drill Size Labeling Error

    Musculoskeletal Transplant Foundation is recalling 117 Allofix Insertion Kits because they are labeled as 2.0mm but may contain 2.4mm drills.

    Product
    Allofix Insertion Kit, 2.0 mm, Single Drill, Product Usage: MTF Surgical Instruments are designed for the specific needs of the orthopedic surgeon and are intended to be used in conjunction with the associated allograft. This kit is for single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1241-2015·2015-07-22

    Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization

    Hospira Inc. is recalling Ketorolac Tromethamine Injections because crystallization was identified as the calcium salt of Ketorolac.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2074-2015·2015-07-22

    Nobel Biocare Recalls Zirconia Abutment Retrieval Instruments Due to Dimensional Error

    Nobel Biocare is recalling 149 units of Zirconia Abutment Retrieval Instruments and Kits because a dimensional error prevents the instruments from removing metal adapters as intended.

    Product
    Abutment Retrieval Instrument Zirconia CC RP/WP, Article No. 37882 and Abutment Retrieval Kit, Article No. 37508 (Article No. 37882 was assembled in this kit). Used to remove a zirconia abutment if the abutment is stuck in the implant connection due to a tight seat. Endosseous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2087-2015·2015-07-22

    Eizo RadiForce GX540 Monitors Recalled for Display Abnormalities

    Eizo is recalling 19 RadiForce GX540 monitors that may display abnormally when connected to specific graphics boards with DisplayPort.

    Product
    RadiForce GX540, 5MP Monochrome LCD Monitor, Part Code No. 0FTD1826A5, 0FTD1826B5, 0FTD1826C5, UPC 690592034752. This product is intended to be used in displaying and viewing digital images including those of digital mammography for review and analysis by trained medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2015·2015-07-22

    Synthes Recalls Helical Blade Inserter for TFNA Due to Sizing Defect

    Synthes (USA) Products LLC is recalling 32 units of the Helical Blade Inserter for TFNA because an oversized pin prevents the tool from passing through the guide sleeve.

    Product
    Helical Blade Inserter for Trochanteric Fixation Nail-ADVANCED (TFNA); intended to secure the head element to the head element inserter to prevent disengagement during head element insertion. Manual orthopedic surgical instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1235-2015·2015-07-22

    Desmopressin Acetate Tablets Recalled for Incorrect Imprint

    American Health Packaging is recalling Desmopressin Acetate Tablets because some are incorrectly imprinted with an X on one side.

    Product
    Desmopressin Acetate Tablets, 0.1 mg Tablets, Rx Only, Packed in 30 Tablet (3 x 10) Cartons. Packaged and Distributed by: American Health Packaging Columbus, Ohio 43217. NDC: 68084-606-21.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2066-2015·2015-07-22

    Tosoh Glycohemoglobin Analyzer Buffer Recalled for Incorrect Expiration Date Labeling

    Tosoh Bioscience is recalling G7 Variant Elution Buffer HiS no. 1 (M) because it is labeled with an expiration date of October 2015 instead of the correct October 2014.

    Product
    G7 Variant Elution Buffer HiS no. 1 (M) component of the Tosoh Automated Glycohemoglobin Analyzer HLC 723G7. Product Usage: G7 Variant Elution Buffer HiS No 1. (M) is one of the buffers used on Tosoh Automated Glycohemoglobin Analyzer HLC 723G7.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2090-2015·2015-07-22

    BD Biosciences Recalls Flow Cytometers for Missing Laser Safety Labeling

    BD Biosciences is recalling 2,188 flow cytometers installed between June 2007 and September 2011 because they lack required FDA laser safety labeling.

    Product
    BD Flow Cytometers; used on all BD FACSCount, BD FACSCalibur, BD FACSCanto, BD FACSCanto II, BD LSR II, BD LSRFortessa,BD FACSAria, BD FACSAria II, BD FACSAria Ill, BD lnflux, BD FACSArray,BD Pathway 855, BD Pathway 435 and all SORP instruments. BD Biosciences Flow cytometers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1238-2015·2015-07-22

    Geritrex Recalls Carb-O-Philic 40 Cream Due to Container Closure Deviation

    Geritrex Corp is recalling Carb-O-Philic 40 Cream due to a CGMP deviation involving poor container closure of the bulk storage container.

    Product
    Carb-O-Philic 40 Cream, 40%, a) 3 oz. tube (NDC 54162-640-03) b) 7 oz. tube (NDC 54162-640-07), Rx Only, Manufactured by Geritrex Corporation, Mount Vernon, NY 10550
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1239-2015·2015-07-22

    Qualitest Recalls HydrOXYzine Tablets Due to Unreadable Identification Codes

    Qualitest Pharmaceuticals is recalling HydrOXYzine Hydrochloride 25 mg tablets because some identification codes are unreadable.

    Product
    HydrOXYzine Hydrochloride Tablets, USP 25 mg, Rx only, 100 count (NDC 0603-3968-21), 500 count (NDC 0603-3968-28) and 1000 count (NDC 0603-3968-32) bottles, Manufactured for Qualitest Pharmaceuticals, Huntsville, AL
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·15189·2015-07-21

    Acorn Stairlifts Recalls Motorized Stair Lifts Due to Fall Hazard

    Acorn Stairlifts is recalling about 34,500 motorized stair lifts because the seat post can separate from the main support, posing a fall hazard.

    Product
    Motorized stair lifts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V454000·2015-07-21

    Allied Recreation Recalls 2016 Motorhomes Due to Propane Regulator Defect

    Allied Recreation Group is recalling 92 model year 2016 motorhomes because an incorrect propane regulator may allow moisture buildup, potentially causing a gas leak and fire.

    Product
    FLEETWOOD — FLEETWOOD, MONACO, HOLIDAY RAMBLER TIOGA RANGER, TREK, TERRA SE, STORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15188·2015-07-21

    Target Recalls Circo Night Lights Due to Fire Hazard

    Target is recalling about 143,000 Circo Night Lights because the battery can overheat and cause the light to melt, posing a fire hazard.

    Product
    Circo Night Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V451000·2015-07-20

    Mazda Recalls 2007-2014 CX-9 Vehicles for Front Suspension Defect

    Mazda is recalling 2007-2014 CX-9 vehicles because front suspension ball joints may corrode, potentially causing loss of steering control and increasing crash risk.

    Product
    MAZDA — MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E061000·2015-07-17

    SAF-Holland Recalls CBX Series Trailer Suspension Systems for Pivot Bolt Failure

    SAF-Holland is recalling CBX series trailer suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer and increasing crash risk.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V450000·2015-07-17

    BMW Recalls 2014-2015 MINI Cooper Models for Side Impact Defect

    BMW is recalling 2014-2015 MINI Cooper, Cooper S, and John Cooper Works vehicles because rear seats fail federal side impact safety standards, increasing injury risk.

    Product
    MINI — MINI JOHN COOPER WORKS, COOPER S, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E062000·2015-07-17

    H&H Sports Protection Recalls VCAN V528 Milano Motorcycle Helmets

    H&H Sports Protection is recalling VCAN V528 Milano motorcycle helmets because the retention systems failed testing and required labeling is missing.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15T014000·2015-07-17

    Continental ContiProContact Tires Recalled for Bead Air Leak Defect

    Continental is recalling specific ContiProContact tires manufactured in early 2015 because a manufacturing error may cause air leaks from the bead area, increasing the risk of sudden tire failure and a crash.

    Product
    TIRES:BEAD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15742·2015-07-17

    EKO Recalls Motion Sensor Trash Cans Due to Laceration Hazard

    EKO is recalling motion sensor trash cans sold at Costco because a protective collar can dislodge, exposing a sharp edge that poses a laceration risk.

    Product
    Trash cans
    Category
    Consumer Product
    Distribution
    Distributed nationwide