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.

50401–50425 of 73995

  • SevereNHTSA·16V015000·2016-01-15

    Coachmen Cross Country Recalled for Fuel Guard Tire Damage Risk

    Forest River is recalling 2016 Coachmen Cross Country vehicles because the fuel fill guard may damage front tires, increasing crash risk.

    Product
    COACHMEN — COACHMEN CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V014000·2016-01-15

    Supreme Recalls Shuttle Buses Due to Wheelchair Lift Bearing Defect

    Supreme is recalling 2008-2014 shuttle buses equipped with certain Ricon wheelchair lifts because pivot holes may allow bearings to move, risking platform failure.

    Product
    STARTRANS — STARTRANS CANDIDATE, SENTINEL BUS, AZURE HYBRID, PRESIDENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V012000·2016-01-14

    Eldorado Recalls 2010-2016 Buses Due to Seat Belt Anchor Weld Defect

    Eldorado is recalling specific 2010-2016 bus models because missing welds on seat brackets could cause seat belts to detach during a crash.

    Product
    ELDORADO — ELDORADO EZRM, XHF, AXESS, ARRIVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16074·2016-01-14

    Steelcase Recalls Rocky Swivel Chairs Due to Fall Hazard

    Steelcase is recalling about 17,000 Rocky model swivel chairs because screws can detach, posing a fall hazard. One injury was reported.

    Product
    Rocky model swivel chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16721·2016-01-14

    School Specialty Recalls NeoRok Stools Due to Fall Hazard

    School Specialty is expanding a recall of NeoRok stools that can break during use, posing a fall hazard to children.

    Product
    Classroom Select NeoRok Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0428-2016·2016-01-13

    Pine Valley Foods Recalls Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Fairytale Princess COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4031 UPC Code - 698768034315
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0464-2016·2016-01-13

    Skinny Latina Marinade Recalled for Undeclared Soy Allergen

    Skinny Latina LLC is recalling 18,822 bottles of Million Dollar Marinade due to undeclared soy. The product was sold at Target, Whole Foods, and Fresh Market.

    Product
    Skinny Latina Million Dollar Marinade, 12 oz, shelf stable, dry storage.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V011000·2016-01-13

    Gillig Recalls 2010-2015 Low Floor Buses Due to Seat Belt Defect

    Gillig is recalling 6,734 Low Floor transit buses from 2010-2015 because missing welds on seat brackets could cause seat belts to detach during a crash.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0433-2016·2016-01-13

    Pine Valley Foods Recalls Cookie Dough for Undeclared Milk and Egg

    Pine Valley Foods is recalling specific batches of pre-portioned cookie dough because they contain undeclared milk or egg allergens.

    Product
    Crazy about Cookies 2.7lb WALNUT CHUNKY CHOCOLATE CHIP Pre-Portioned cookie dough Item # 25-2008 UPC Code - 698768102168
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0427-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Holiday Gathering COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4034 UPC Code - 698768034346
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0420-2016·2016-01-13

    ConAgra Recalls David Trail Mix Sweet & Salty for Undeclared Milk

    ConAgra Foods is recalling David Trail Mix Sweet & Salty bags because they contain undeclared milk. The product was distributed nationwide and to specific foreign locations.

    Product
    David Trail Mix Sweet & Salty individual plastic bags net wt. 5 oz. (142 g) UPC 00 26200 23885 2 shipped in the following configurations: 1) cases of eight (8) with UPC 20-0-26200-23885-6; 2) 36-count multi-pack shipper case UPC 00-0-26200-23890-6 which contains 16…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0588-2016·2016-01-13

    Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recall for Handle Separation

    Boston Scientific is recalling ACUITY Pro Coronary Sinus Guide Catheters due to a potential for the proximal handle to separate from the shaft.

    Product
    Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr. Model 8104, 8105, 8106, 8107, 8108, 8109, 8110, 8111, 8112, 8113, 8114, 8115, 8116, 8117, 8118, and 8119. The ACUITY Pro Lead Delivery System is designed for venous use to aid in the selective placement of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0426-2016·2016-01-13

    Pine Valley Foods Recalls Sugar and Walnut Cookie Dough for Allergens

    Pine Valley Foods is recalling pre-portioned sugar and walnut chocolate chunk cookie dough because they contain undeclared milk and egg, respectively.

    Product
    Crazy about Cookies 2.7lb Sugar Cookies Pre-Portion Item # 25-2004 UPC Code - 698768102120
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0430-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Birthday Celebration COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4033 UPC Code - 698768034339
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0432-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookies for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie products due to undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb DSC Custom Decorated Sugar Cookies Item # 101-2207 thru 101- 2355 UPC Code - None
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0429-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific sugar cookie kits because they contain undeclared milk and egg allergens.

    Product
    Crazy about Cookies 2lb Monster Bash COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4032 UPC Code - 698768034322
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0431-2016·2016-01-13

    Pine Valley Foods Recalls Sugar Cookie Kits for Undeclared Allergens

    Pine Valley Foods is recalling specific Hello Kitty sugar cookie kits because they contain undeclared milk and egg.

    Product
    Crazy about Cookies 2lb HELLO KITTY COLLECTION Decorated SUGAR COOKIE KIT Item # 03-4035 UPC Code - 698768034353
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0592-2016·2016-01-13

    Biomet 3i Protection Cap Kits Recalled for Inadequate Biocompatibility Testing

    Biomet 3i is recalling 30,111 Protection Cap Kits worldwide due to inadequate biocompatibility testing. The devices are used as accessories for dental implants.

    Product
    BIOMET 3i, PROVIDE PROTECTION CAP KITS, Catalog # PAK4140, PAK4155, PAK4240, PAK4255, PAK4340, PAK4355, PAK4440, PAK4455, PAK5140, PAK5155, PAK5240, PAK5255, PAK5340, PAK5355, PAK5440, PAK5455, PAK6140, PAK6155, PAK6240, PAK6255, PAK6340, PAK6355, PAK6440, and PAK6455 BIOMET…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0574-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 1,406 post-operative knee braces because they may fail to maintain a locked position, potentially causing loss of balance or undesired knee movement.

    Product
    Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 10 units of the Brielle Ortho Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.

    Product
    BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0577-2016·2016-01-13

    Corflex Post-Operative Knee Brace Recalled for Potential Locking Failure

    Corflex is recalling 42 units of the Contender Post-Op-Knee Brace Lite because the brace may fail to maintain its locked position, potentially causing loss of balance or undesired knee movement.

    Product
    ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Operative Knee Brace is indicated for range of motion control at the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable…
    Category
    Medical Device
    Distribution
    Distributed nationwide