The Recall Desk

State

US Virgin Islands product recalls

73,381 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20551–20575 of 73558

  • HighNHTSA·22V397000·2022-06-07

    Kawasaki Recalls LX230 Motorcycles Due to Brake Rotor Defect

    Kawasaki is recalling 2020-2022 LX230 motorcycles because an incorrect front brake rotor may have been installed, reducing brake performance and increasing crash risk.

    Product
    KAWASAKI — KAWASAKI LX230G, LX230A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V401000·2022-06-07

    2021-2022 Mack trucks recalled for defective steering gears

    Mack Trucks is recalling certain 2021-2022 tractor trailers due to steering gears that may fracture, causing loss of steering control and crash risk.

    Product
    MACK — MACK PINNACLE (PI/PN), TE, ANTHEM (AN), GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V396000·2022-06-06

    Micro Bird Recalls 2017-2018 G5 School Buses Due to Seat Belt Defect

    Micro Bird is recalling 2017-2018 G5 school buses because an incorrect bracket may interfere with the driver's seat belt pretensioner, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V395000·2022-06-06

    Forest River Recalls 2022 Travel Trailers Due to Table Weld Defect

    Forest River is recalling 2022 East to West Alta and Palomino SolAire travel trailers because incomplete welds on the swing-up table base may cause it to drop unexpectedly, increasing injury risk.

    Product
    EAST TO WEST — EAST TO WEST, PALOMINO ALTA, SOLAIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V394000·2022-06-03

    2023 Freightliner M2 Trucks Steering Shaft Defect Recall

    Daimler Trucks North America is recalling 2023 Freightliner Business Class M2 trucks due to a u-joint pinch bolt that may detach from the steering shaft, causing loss of steering control and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 114SD, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T009000·2022-06-02

    Goodyear Recalls G159 Tires Due to Tread Separation Risk

    Goodyear is recalling specific G159 tires because the tread may separate, increasing the risk of a crash. Owners should contact dealers for free replacement.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22147·2022-06-02

    Backcountry Access Tracker4 Avalanche Transceivers Recalled for Toggle Switch Failure

    Backcountry Access Tracker4 Avalanche Transceivers are being recalled because the toggle switch can separate from the unit and prevent it from switching to search mode, which could prevent rescuers from locating a buried skier.

    Product
    Backcountry Access Tracker4 Avalanche Transceivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22146·2022-06-02

    Asweets Recalls Wonder & Wise Baby Activity Walkers for Strangulation Hazard

    Asweets is recalling about 13,300 Wonder & Wise baby activity walkers because rubber rings on the rear wheels can detach, posing a strangulation hazard to young children. No injuries have been reported.

    Product
    Wonder & Wise Baby Activity Walkers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22141·2022-06-02

    Communicorp Recalls Aflac Plush Promotional Ducks for Phthalates and Lead

    Communicorp is recalling about 600,000 six-inch Aflac plush promotional ducks distributed to Aflac employees and customers from February 2009 through March 2021. The ducks contain phthalates and lead levels that exceed federal standards and pose a risk if ingested by young children.

    Product
    6" Aflac Plush Promotional Ducks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22145·2022-06-02

    Children's Robes Recalled Due to Burn Hazard

    Joey Clothing is recalling about 15,930 children's robes sold online because they fail to meet flammability standards for children's sleepwear, posing a risk of burn injuries.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V393000·2022-06-02

    Winnebago Recalls 2020 ERA Motorhomes Due to Gas Leak Risk

    Winnebago is recalling 2020 ERA motorhomes because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    WINNEBAGO — WINNEBAGO ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22144·2022-06-02

    Demdaco Microwavable Bowl Holders Recalled for Fire Hazard

    Demdaco microwavable bowl holders can char and catch fire when microwaved for the recommended time. The company received three reports of charring incidents and is offering refunds.

    Product
    Microwavable bowl holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22143·2022-06-02

    Frigidaire and Electrolux Refrigerators Recalled for Ice Maker Choking Hazard

    Electrolux is recalling about 367,500 Frigidaire and Electrolux refrigerators because the ice level detector arm in the ice maker can break apart and fall into the ice bucket, creating a choking hazard.

    Product
    Frigidaire and Electrolux Side-by-Side, Top Freezer and Multi-door refrigerators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22142·2022-06-02

    Target Recalls Children's Cat & Jack Unicorn Cozy Pajama Sets for Burn Hazard

    Target is recalling about 120,000 children's pajama sets because they fail to meet federal flammability standards for sleepwear, posing a burn injury risk to children. Consumers should return the pajamas to Target for a full refund.

    Product
    Children's pajama sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V392000·2022-06-02

    2022 Cadillac XT6 brake fluid reservoir cap warning label missing

    General Motors is recalling certain 2022 Cadillac XT6 vehicles because the brake fluid reservoir cap may be missing its required warning label. Without the label, brake fluid could become contaminated with debris, affecting brake performance.

    Product
    CADILLAC — CADILLAC XT6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1098-2022·2022-06-01

    Sara Plus Active Floor Lift Recalled for Smoke and Ignition Risk

    The FDA is recalling approximately 4,449 Sara Plus Active Floor Lift devices due to a fire hazard. The devices may emit smoke or ignite, posing a risk to users and staff.

    Product
    Sara Plus Active Floor Lift
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0925-2022·2022-06-01

    FDA Recalls Compounded Injectable for Lack of Sterility Assurance

    Olympia Compounding Pharmacy recalls a multi-drug injectable compound (lot B41C22-22) due to inability to assure sterility. The recall affects 1,159 vials distributed nationwide.

    Product
    FA Papaverine 20 mg/mL Phentolamine 2 mg/mL Alprostadil 20 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial, Rx Only, 6700 Olympia Pharmaceuticals, Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0006-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0943-2022·2022-06-01

    Ondansetron Hydrochloride vials recalled due to sterility assurance concerns

    Olympia Compounding Pharmacy recalls 911 vials of Ondansetron Hydrochloride (1 mg/mL) due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and US Virgin Islands.

    Product
    Ondansetron Hydrochloride, 1 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0127-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·22V390000·2022-06-01

    Adam Horse Trailer Recall for Damaged Cooktop Burner Valves

    Dalton Enterprises is recalling 2021-2022 Adam J2040 horse trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    ADAM — ADAM HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0945-2022·2022-06-01

    FDA Recalls Phenylephrine 1 mg/mL Vials for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling 9,102 vials of Phenylephrine 1 mg/mL due to lack of assurance of sterility. The affected vials were distributed nationwide in the United States, Puerto Rico, and US Virgin Islands.

    Product
    Phenylephrine 1 mg/mL, Multi-Dose 5 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0021-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0933-2022·2022-06-01

    Compounded pharmaceutical vials recalled due to sterility assurance failure

    Olympia Compounding Pharmacy is recalling Lipostat-Plus vials nationwide due to lack of sterility assurance. Approximately 4,843 vials were distributed across the USA, Puerto Rico, and US Virgin Islands.

    Product
    Lipostat-Plus Methionine 25 mg/mL Inositol 50 mg/mL Choline Chloride 50 mg/mL Cyanocobalamin 1 mg/mL Pyridoxine HCL 175 mcg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0047-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0905-2022·2022-06-01

    Sodium Selenite Injectable Vials Recalled for Sterility Assurance Failure

    Olympia Compounding Pharmacy recalls 2,333 vials of Sodium Selenite 200 mg/mL injection due to a lack of assurance of sterility. The product was distributed nationwide in the USA, Puerto Rico, and the U.S. Virgin Islands.

    Product
    Sodium Selenite 200 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0074-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0899-2022·2022-06-01

    Compounded Injectable Medication Recalled Due to Sterility Assurance Concerns

    Olympia Compounding Pharmacy recalled 1,710 vials of RE-2 injectable medication due to lack of assurance of sterility. Affected vials were distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.

    Product
    RE-2 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL, Packaged as a) 2.5 mL Multi Dose vial, NDC 73198-0016-03; b) 10 mL Multi Dose vial, NDC 73198-0016-10; Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0935-2022·2022-06-01

    Magnesium Chloride injection recalled due to lack of sterility assurance

    Olympia Compounding Pharmacy is recalling 1,597 vials of Magnesium Chloride injection due to lack of sterility assurance. The product was distributed nationwide in the USA, Puerto Rico, and the US Virgin Islands.

    Product
    Magnesium Chloride, 200 mg/mL, Multi-Dose 30 mL vial, Rx Only, Olympia Pharmaceuticals, 6700 Conroy Rd., Ste. 155 Orlando, FL 32835. NDC 73198-0072-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0900-2022·2022-06-01

    Compounded Injectable Drug Recalled for Lack of Sterility Assurance

    Olympia Compounding Pharmacy is recalling SB-5, a multi-dose injectable medication, due to lack of assurance of sterility. The product was distributed nationwide; patients should contact their healthcare provider immediately.

    Product
    SB-5 Papaverine 30 mg/mL Phentolamine 3 mg/mL PGE 50 mcg/mL, Multi-Dose 10 mL vial, Rx Only, Olympia Pharmaceuticals 6700 Conroy Rd., Ste. 155 Orlando, FL 32835, NDC 73198-0024-10
    Category
    Drug
    Distribution
    Distributed nationwide