The Recall Desk

State

US Virgin Islands product recalls

73,509 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
2026-10-14

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.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25201–25225 of 73686

  • ModerateFDA (Devices)·Z-1436-2021·2021-04-28

    Stryker DirectInject Bone Cement Recalled Due to Injection Failure

    Stryker is recalling 321 units of DirectInject bone cement because the paste cannot be injected from the syringe into the target location.

    Product
    DirectInject consists of a sterile dual paste system which is calcium phosphate based. Upon injection through the Mixer-Cannula, the two pastes form a cement paste which is moldable. The injected cement paste will harden under normal body conditions to form hydroxyapatite.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1469-2021·2021-04-28

    HeartWare HVAD Instructions for Use and Patient Manual Recall

    Heartware, Inc. is recalling Instructions for Use and Patient Manuals for the HeartWare HVAD System to update guidance on intermittent alarm issues.

    Product
    Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these devices: Heartware HVAD pump implant kits Models 1100, 1101, 1102, 1103, 1104, 1104JP, 1205, and MCS1705PU. Heartware HVAD controller kits Models 1403US, 1407AU, 1407CA, 1407CH, 1407DE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0336-2021·2021-04-28

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defects

    Noven Pharmaceuticals is recalling Minivelle estradiol transdermal patches because the adhesive may not stick well to the skin.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1440-2021·2021-04-28

    Medtronic Endoskeleton TC Interbody System Recalled for Packaging Labeling Error

    Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes were mislabeled, containing the wrong size device.

    Product
    Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Large, 8 mm, Product Number 5146-1608-N - Product Usage: indicated to be used with supplemental fixation cleared by the FDA for use in the cervical spine and autograft bone, allograft bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1431-2021·2021-04-28

    Bard Clean-Cath Intermittent Catheter Recalled for Packaging and Tip Defects

    C.R. Bard is recalling 9,800 units of Bard Clean-Cath Intermittent Catheters because the catheter tip was cut off and the packaging was not fully sealed.

    Product
    Bard Clean-Cath Intermittent Catheter, 12 French female length (catheter, urological) - Product Usage: for urological use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1432-2021·2021-04-28

    Azure Biotech Recalls Assure COVID-19 Rapid Test Devices for Labeling Errors

    Azure Biotech Inc. is recalling 100,000 Assure COVID-19 IgG/IgM Rapid Test Devices due to incorrect diagnostic labeling and unsupported expiration dating.

    Product
    Assure COVID-19 IgG/IgM Rapid Test Device that include: 1) Pouch Label - FaStep Rapid Diagnostic Test *** Rapid Reliable Simple *** COVID-19 IgG/IgM Rapid Test Device (Whole blood/Serum/Plasma) *** For Emergency Use Authorization Only, Box Label - FaStep Rapid Diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1439-2021·2021-04-28

    Medtronic Endoskeleton TC Interbody System Recalled for Incorrect Size Labeling

    Medtronic is recalling 11 Endoskeleton TC Interbody System devices because shelf boxes misidentify the size of the contained device.

    Product
    Endoskeleton TC Interbody System with Titan nanoLOCK Surface Technology, 6 Degree, Small, 8 mm, Product Number 5146-1208-N - Product Usage: indicated to be used with supplemental fixation cleared by the FDA for use in the cervical spine and autograft bone, allograft bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1484-2021·2021-04-28

    Welch Allyn Surveyor Bedside Patient Monitor Recalled for Safety Standard Non-Compliance

    Welch Allyn is recalling 213 Surveyor S12/S19 Bedside Patient Monitors because they do not meet IEC 60601-2-27 safety requirements as labeled.

    Product
    Surveyor S12/S19 Bedside Patient Monitor, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1483-2021·2021-04-28

    Welch Allyn ELI 380 Electrocardiograph Recalled for IEC 60601-2-27 Non-Compliance

    Welch Allyn Inc Mortara is recalling 27 ELI 380 Electrocardiographs because they do not meet IEC 60601-2-27 requirements as labeled.

    Product
    ELI 380 Electrocardiograph, with AM12M Acquisition Module accessory. Impacted software version of the AM12M is version 1.5.1 - Product Usage: indicated for use on adult and pediatric populations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0335-2021·2021-04-28

    Edge Pharma Recalls Betadine Ophthalmic Syringes Due to Sterility Concerns

    Edge Pharma is recalling 5,850 syringes of Betadine ophthalmic solution because a defective container may compromise sterility. The product is distributed nationwide.

    Product
    Betadine (Povidone-Iodine) 5%, 0.5mL per syringe Single Use Syringe Rx only, For Topical Ophthalmic Use (DO NOT INJECT) STERILE OPHTHALMIC SOLUTION, PRESERVATIVE FREE, Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 Customer Service (USA) 1-802-992-1178
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1438-2021·2021-04-28

    HeartWare HVAD Instructions for Use and Patient Manual Labeling Correction

    Heartware, Inc. is recalling Instructions for Use and Patient Manuals for the HVAD System to correct inaccurate descriptions of controller connection verification.

    Product
    Instructions for Use and Patient Manual for HeartWare HVAD System. Accompanies these devices: Heartware HVAD pump implant kits Models 1100, 1101, 1102, 1103, 1104, 1104JP, 1205, and MCS1705PU. Heartware HVAD controller kits Models 1403US, 1407AU, 1407CA, 1407CH, 1407DE…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V297000·2021-04-27

    Mitsubishi Fuso Recalls FEC7T Trucks for Rear Leaf Spring Defect

    Mitsubishi Fuso is recalling 2019-2021 FEC7T trucks because the rear leaf spring may break, creating a road hazard and increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC7T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V295000·2021-04-26

    Multiple Audi vehicles recalled for defective rear axle suspension lock nuts

    Audi is recalling certain 2019-2021 vehicles for rear axle lock nuts that may break from stress corrosion. A broken lock nut can cause axle misalignment, loss of control, and increased crash risk.

    Product
    AUDI — AUDI S5 CABRIOLET, S5, S4, RS 7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V292000·2021-04-26

    Keystone Recalls 2021 Passport Trailers Due to Underrated Safety Chains

    Keystone is recalling specific 2021 Passport trailers because the installed safety chains are underrated for the vehicle's weight rating, which could allow the trailer to detach from the tow vehicle.

    Product
    KEYSTONE — KEYSTONE PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·015-2021·2021-04-24

    More Than Gourmet Recalls Beef and Veal Broth Due to Hydraulic Oil Contamination

    More Than Gourmet is recalling beef and veal broth products that may contain hydraulic oil. No illnesses have been reported.

    Product
    Ajinomoto Health & Nutrition North America — More Than Gourmet, Inc. Recalls Beef And Veal Broth And Stock Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V288000·2021-04-23

    Mercedes-Benz Recalls 2020-2021 GLE and GLS Models for Fire Risk

    Mercedes-Benz is recalling certain 2020-2021 GLE and GLS vehicles because incorrectly installed air conditioner drain hoses may cause water intrusion, leading to electrical short circuits and fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, GLS 450, GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·014-2021·2021-04-23

    Super World Trading Recalls Ineligible Imported Ready-to-Eat Fish Chips

    Super World Trading Inc. is recalling approximately 26,270 pounds of ready-to-eat fish chips imported from China because the country is ineligible to export processed products to the U.S.

    Product
    Super World Trading Inc. Recalls Ineligible Ready-To-Eat Siluriformes Products Imported From China
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V287000·2021-04-23

    2021 Coachmen Catalina Travel Trailer Recall for Fire Risk

    Forest River is recalling 2021 Coachmen Catalina travel trailers because an incorrectly gauged battery wire may melt and cause a fire.

    Product
    COACHMEN — COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V289000·2021-04-23

    REV Ambulance Recalls 2019-2021 Type I and IX Vehicles for Display Defect

    REV Ambulance Group Orlando is recalling 2019-2021 Type I and IX ambulances because LCD displays may lock up, potentially delaying emergency efforts.

    Product
    ROAD RESCUE — ROAD RESCUE, WHEELED COACH TYPE III, TYPE IX, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V290000·2021-04-23

    Rosenbauer Fire Trucks Recalled for Excessively Bright Rear Lights

    Rosenbauer America is recalling specific fire trucks because rear lights may be too bright, potentially blinding other drivers and increasing crash risk.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL 7400, COMMERCIAL M2-106, COMMERCIAL HV613
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V284000·2021-04-22

    Blue Bird Recalls 2020-2022 School Buses Due to Brake Valve Defect

    Blue Bird is recalling 2020-2022 Vision and All American school buses because a check valve may fail to isolate air, potentially causing unintended spring brake application and increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V285000·2021-04-22

    Blue Bird Recalls 2022 Transit Buses Due to Air Brake Defect

    Blue Bird is recalling 96 2022 Vision and All American transit buses because a check valve defect may cause unintended spring brake application, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide