The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

60951–60975 of 74011

  • HighNHTSA·13V586000·2013-11-21

    Carry-On Enclosed Cargo Trailer Recall for Door Lock Jamming Risk

    Carry-On is recalling 2006-2013 enclosed cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    CARRY-ON — CARRY-ON ENCLOSED CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V590000·2013-11-21

    Collins Recalls 2013 School Buses Due to Seat Belt Buckle Defect

    Collins Bus Corporation is recalling 333 model year 2013 school buses because seat belt buckles may fail to release, hindering emergency egress.

    Product
    COLLINS — COLLINS, COLLINS MID BUS, COLLINS CORBEIL DE516WR, DE516, DH416WR, DH400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V587000·2013-11-21

    HL Enterprise Recalls 2011-2013 Trailers With Defective Door Locks

    HL Enterprise is recalling 716 model year 2011-2013 travel, fifth-wheel, and destination trailers equipped with Fastec-brand door locks that may jam, potentially trapping occupants inside.

    Product
    BRIDGEVIEW — BRIDGEVIEW, GEORGIAN BAY, HARBORVIEW TRAVEL/5TH/DESTINATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14029·2013-11-21

    Cuisinart Recalls 7-Cup Food Processors Due to Laceration Hazard

    Cuisinart is recalling 7-cup food processors because a loose slicing disc can break the cover, posing a laceration hazard to consumers.

    Product
    Cuisinart 7-cup food processors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1732-2013·2013-11-20

    Priester's Pecans Roasted Nuts Recalled for Salmonella Risk

    Priester Pecan Company is recalling Fancy Roasted Nuts because pistachios supplied by ARO may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand FANCY ROASTED NUTS, Stock No. 7, Net Wt 12 oz (454g)
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1731-2013·2013-11-20

    Priester's Pecans Nutty Favorites Recalled for Salmonella Risk

    Priester Pecan Company is recalling Nutty Favorites Assortments because supplied pistachios may be contaminated with Salmonella.

    Product
    PRIESTER'S PECANS brand NUTTY FAVORITES ASST, Stock No. 79, Net Wt 1 lb 10 oz (737g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0202-2014·2013-11-20

    Synthes 8.5 MM Medullary Reamer Recalled Due to Intraoperative Breakage

    Synthes USA HQ, Inc. is recalling 2,979 units of the 8.5 MM Medullary Reamer because the reamer head can break during surgery, leaving unretrieved fragments of non-implant grade material.

    Product
    Synthes 8.5 MM Medullary Reamer Product Usage: An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0280-2014·2013-11-20

    Stryker Recalls Acetabular Pressurizers Due to Cracked Assemblies

    Stryker is recalling 87 boxes of Acetabular Pressurizers because cracked assemblies may release during cement application.

    Product
    Acetabular Pressurizer; single use and six units per box. The Acetabular Pressurizer 0206-522-000 is an accessory to the Advanced Cement Mixer (ACM). The Acetabular Pressurizer Tiplet P/N 0206-522-012 is sealed in a two pouches, sterilized, and labeled as part number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0175-2014·2013-11-20

    GoPicnic Hummus and Crackers Meal Kits Recalled for Undeclared Milk

    GoPicnic is recalling Hummus & Crackers meal kits because the included chocolates may contain undeclared milk allergens.

    Product
    Gopicnic; Hummus & crackers; GoPicnic meal kit packaged in paperboard container. ready-to-eat meal; with professor zim zam's extraordinary sweets dark chocolate with sea salt. NET WT 4.1 OZ (116g); distributed by gopicnic brands, inc.; chicago, il 60613; www.gopicnic.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V588000·2013-11-20

    Nissan Recalls 2014 Infiniti Q50 for Steering Software Defect

    Nissan is recalling 2014 Infiniti Q50 vehicles because freezing temperatures may disable electric steering and delay the mechanical backup, increasing crash risk.

    Product
    INFINITI — INFINITI Q50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0174-2014·2013-11-20

    GoPicnic Meal Kits Recalled for Undeclared Milk Allergen

    GoPicnic is recalling Black Bean Dip & Plantain Chips meal kits because the included chocolates may contain undeclared milk allergens.

    Product
    GoPicnic Black Bean Dip & Plantain Chips; ready-to-eat meal kit with professor zim zam's extraordinary sweets dark chocolate with orange packaged in paperboard container; NET WT 4.2 OZ (116.2g); distributed by gopicnic brands, inc.; chicago, il 60613; www.gopicnic.com;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0205-2014·2013-11-20

    Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Drift

    Hospira is recalling 71 Plum A+ Infusion Pumps because pressure sensor calibration drift can cause false alarms or missed occlusions.

    Product
    Plum A+ Infusion Pump; List Number: 11973; Product Usage: The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0186-2014·2013-11-20

    Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis

    Fresenius Medical Care is recalling 508,029 cases of Combiset Blood Lines for hemodialysis because connections may disconnect if not tightened correctly, leading to blood loss.

    Product
    Combiset Blood Line Hemodialysis use Catalog Number: 03-2622-3. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0144-2014·2013-11-20

    Apex Energetics Recalls Four Enzyme Supplements Due to Chloramphenicol Contamination

    Apex Energetics is recalling four enzyme-based dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol.

    Product
    RepairVite (K63), Enzyme-Based Herbal & Amino Acid Dietary Supplement Powder, Caramel Flavor, Net Wt. 0.34 lb (155g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V582000·2013-11-20

    Jet Co Aluminum Grain Trailers Recalled for Weak Top Rail

    Jet Co is recalling 2011-2012 aluminum grain trailers because a weak top rail may buckle, increasing crash risk.

    Product
    JET CO — JET CO ALUMINUM GRAIN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1730-2013·2013-11-20

    Priester's Pecans Pistachios Recalled for Potential Salmonella Contamination

    Priester Pecan Company is recalling specific lots of roasted salted pistachios due to potential Salmonella contamination. The product was distributed nationwide and in Puerto Rico.

    Product
    PRIESTER'S PECANS brand brand ROASTED SALTED PISTACHIOS, item #18010, Net Wt. 1 lb (454g), UPC 720056180104; item #15502, Net Wt. 8 oz (226.8g), UPC 001001155027; Stock No. 189, Net Wt. 2 lb (907g)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0171-2014·2013-11-20

    Aunt Jemima Quick Grits Recalled for Aflatoxin Contamination

    Quaker Foods and Snacks North America is recalling Aunt Jemima Quick Grits because some bags contain aflatoxin levels above the legal limit.

    Product
    White grits packaged in a paper bag labeled in part: Smooth & Creamy; Aunt Jemima; Quick GRITS; Cooks in about 5 minutes; ENRICHED WHITE HOMINY; NET WT 36.8 oz. (2 lb. 4.8 oz.) 1043g
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0172-2014·2013-11-20

    Aunt Jemima Grits and Corn Meal Recalled for Aflatoxin Levels

    Quaker Foods and Snacks North America is recalling specific lots of Aunt Jemima Quick Grits and Corn Meal Mix because they contain aflatoxin above legal limits.

    Product
    White grits packaged in a paper bag labeled in part: Smooth & Creamy; Aunt Jemima; Quick GRITS; Cooks in about 5 minutes; ENRICHED WHITE HOMINY; NET WT 36.8 oz. (2 lb. 4.8 oz.) 1043g
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0185-2014·2013-11-20

    Fresenius Medical Care Recalls Combiset Blood Lines for Hemodialysis

    Fresenius Medical Care is recalling 24,202 cases of Combiset Blood Lines with BVM for hemodialysis. The recall addresses a risk of blood loss if connections are not tightened correctly.

    Product
    Combiset Blood Line with BVM for Hemodialysis use Catalog Number: 03-2965-9. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2014·2013-11-20

    Hospira Recalls Plum A+ Infusion Pumps Due to Pressure Sensor Calibration Drift

    Hospira is recalling Plum A+ Infusion Pumps because pressure sensor calibration drift may cause false occlusion alarms or missed occlusions.

    Product
    *** 1) Plum A+ Infusion Pump; List Number: 20678; Labeled in part: PLUM A+3; for use with Hospira MedNet; *** 2) Plum A+ Infusion Pump; List Number: 20679; Labeled in part: PLUM A+; for use with Hospira MedNet; *** 3) Plum A+ Infusion Pump with Hospira MedNet…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V579000·2013-11-20

    Blue Bird Recalls 2014-2015 School Buses for Seat Belt Defect

    Blue Bird is recalling 2014-2015 Vision and All American school buses because the driver's seat belt latch may fail to release, hindering emergency egress.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0143-2014·2013-11-20

    Apex Energetics Recalls Four Supplements Due to Chloramphenicol Contamination

    Apex Energetics is recalling four dietary supplements because they may contain trace amounts of the antibiotic chloramphenicol from a raw material supplier.

    Product
    LGS-Zyme (Z12), Enzyme-Based Multivitamin & Amino Acid Dietary Supplement, 120 Capsules
    Category
    Food
    Distribution
    Distributed nationwide