The Recall Desk

State

US Virgin Islands product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23176–23200 of 73655

  • ModerateFDA (Devices)·Z-0020-2022·2021-10-13

    Orthopedic Knee Implants Lack Protective Oxygen Barrier in Packaging

    Exactech OPTETRAK Comprehensive Knee System inserts were packaged in vacuum bags lacking an additional oxygen barrier layer, which could allow material degradation. The recall affects 2,774 devices distributed worldwide.

    Product
    OPTETRAK Comprehensive Knee System including OPTETRAK All-polyethylene UNI Tibial Components, Product Lines, 252-12-XX, 252-13-XX, 252-22-XX, 252-23-XX. NOTE: Information reflects Exactech recall expansion initiated on 02/07/2022.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0039-2022·2021-10-13

    Zoll ICY Intravascular Catheter Kit: Labeling Update on Potential Leaks

    ZOLL is updating labeling for ICY Intravascular Heat Exchange Catheter Kits due to potential leaks in the catheter or tubing. Healthcare providers should review updated guidance from the manufacturer.

    Product
    Zoll REF: 8700-0782-01 (IC-3893), ICY Intravascular Heat Exchange Catheter Kit, with central venous infusion capabilities (3 lumens) , Femoral vein Insertion Only, Sterile EO, Rx Only, UDI: (01)00849111075237
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0019-2022·2021-10-13

    OPTETRAK Comprehensive Knee System components recalled for inadequate packaging barrier

    Exactech is recalling approximately 242,397 OPTETRAK Comprehensive Knee System tibial components due to inadequate oxygen barrier in vacuum bag packaging. No injuries have been reported.

    Product
    OPTETRAK Comprehensive Knee System, labeled as the following: a. OPTETRAK All-polyethylene CR Tibial Components, with Product Line Numbers: 200-11-XX, 200-12-XX, 200-13-XX, 200-14-XX, 200-15-XX, 200-16-XX; b. OPTETRAK All-polyethylene PS Tibial Components, with Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0037-2022·2021-10-13

    Medical cooler-heater device recalled for inadequate maintenance and inspection guidance

    CardioQuip is recalling 1,646 units of its Modular Cooler-Heater 1000(m) due to inadequate labeling. The device documentation lacks guidance on proper water-quality maintenance and inspection procedures required for safe operation.

    Product
    CardioQuip, Modular Cooler-Heater 1000(m),Compact Unit, Model:MCH-1000(m),CE 2797, UDI: (01)00860000846110
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0038-2022·2021-10-13

    Cardiac Cooler-Heater Device Lacks Maintenance and Inspection Guidance

    CardioQuip is recalling its Modular Cooler-Heater device because labeling omits proper guidance for water-quality maintenance and device inspection, affecting users' ability to maintain the device correctly.

    Product
    CardioQuip, Modular Cooler-Heater 1000(m),Thermoelectric Cooling Lid, Model: MCH-11TEC,CE 2797, UDI: (01) 00860000846134
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0050-2022·2021-10-13

    Zoll ICY Heat Exchange Catheter Kit Labeling Update Due to Potential Leaks

    ZOLL Circulation is updating labeling for its ICY Intravascular Heat Exchange Catheter Kit due to potential leaks in the catheter or start-up kit tubing. The recall affects 1,256 units distributed worldwide.

    Product
    Zoll REF: 8700-0782-14 (IC-3893CO), ICY Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, Sterile EO, Rx Only, UDI: (01)00849111075527
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0017-2022·2021-10-13

    Scan Abutment PCA dental implant component recalled for tolerance deviations

    Paltop Advanced Dental Solutions is recalling Scan Abutment PCA devices due to manufacturing tolerance deviations that may delay implant restoration. Some devices show up to 2-degree orientation variance and sizing discrepancies.

    Product
    Scan Abutment PCA, Cat. No. 30-70105 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0022-2022·2021-10-13

    OPTETRAK Comprehensive Knee System Custom Inserts Recalled for Packaging Defect

    Exactech, Inc. is recalling 41 custom OPTETRAK knee implant inserts due to packaging defects. The inserts were packaged in vacuum bags lacking adequate oxygen barrier protection.

    Product
    OPTETRAK Comprehensive Knee System custom devices labeled as the following: a. CUSTOM OPTETRAK ANGLED PS INSERT (Product Line: 900-06-XX, 900-08-XX); b. CUSTOM OPTETRAK CC TIBIAL INSERT (Product Line: 900-23-XX, 900-30-XX); c. CUSTOM OPTETRAK CC INSERT (Product Line…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0016-2022·2021-10-13

    Dental implant abutments recalled for orientation and sizing tolerance issues

    Paltop Advanced Dental Solutions is recalling Scan Abutment SU devices (Catalog No. 30-70104) manufactured before July 21, 2021, due to manufacturing tolerance deviations that may delay dental restoration.

    Product
    Scan Abutment SU, Cat. No. 30-70104 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0018-2022·2021-10-13

    Dental implant scan abutment recalled for dimensional tolerance and marking defects

    Paltop Scan Abutment WP dental implant scanning devices are recalled due to manufacturing defects. Affected units show dimensional tolerance deviations and size marking incongruences that may delay restoration procedures.

    Product
    Scan Abutment WP, Cat. No. 30-70106 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0014-2022·2021-10-13

    Scan Abutment NP Dental Implant Components Recalled for Dimensional Deviations

    Paltop Advanced Dental Solutions is recalling Scan Abutment NP dental implant components due to manufacturing tolerance deviations that may affect implant restoration fit and timing.

    Product
    Scan Abutment NP, Cat. No. 30-70102 - Product Usage: used to take an impression with an intra oral scanner or optical scanner to provide a digital registration of an implant or abutment platform. The Paltop Advanced Dental Solutions Implant System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0043-2022·2021-10-13

    ZOLL SOLEX 7 Intravascular Catheter Kit Labeling Update for Potential Leaks

    ZOLL Circulation, Inc. is updating labeling for SOLEX 7 intravascular heat exchange catheter kits to communicate about potential leaks from the catheter or start-up kit tubing. The update affects 5,345 kits with worldwide distribution.

    Product
    ZOLL, REF 8700-0793-40 (SL-2593AE) SOLEX 7, Intravascular Heat Exchange Catheter Kit with central venous infusion capabilities (3 lumens), HEPARIN COATED, Sterile EO, Rx Only, UDI: (00)849111075312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V792000·2021-10-12

    KTM and Husqvarna Recall Motorcycles for Clutch Slave Cylinder Defect

    KTM North America is recalling specific 2018-2020 KTM and Husqvarna motorcycles because a damaged gasket on the clutch slave cylinder may prevent the clutch from disengaging, increasing crash risk.

    Product
    KTM — KTM, HUSQVARNA 690 ENDURO R, 701 ENDURO LR, 690 DUKE, ENDURO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V793000·2021-10-12

    2019-2022 Winnebago Travato and Boldt RV Electrical Fire Hazard

    Winnebago is recalling 2019-2022 Travato and 2021-2022 Boldt RVs. A faulty wire harness may lose over-current protection, causing wires to overheat and increasing fire risk. Owners must not drive until the Volta Power System is disabled.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, BOLDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V789000·2021-10-11

    Mercedes-Benz Recalls 2021 S-Class Models for Air Bag Software Defect

    Mercedes-Benz is recalling 2021 S 500 and S 580 vehicles because a software defect may deactivate the front passenger air bag, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ S 500, S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V790000·2021-10-11

    HME Recalls 2017-2020 Fire Trucks Due to Fuel Rail Leak Risk

    HME is recalling 245 fire trucks from 2017-2020 because a sealing washer may not seat correctly, allowing the high-pressure fuel rail to leak and increasing fire risk.

    Product
    HME — HME, HME AHRENS-FOX 1871, COMMFOX, AERIAL, AF1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V788000·2021-10-09

    Foretravel Recalls 2020-2022 RVs Due to Window Adhesive Failure

    Foretravel is recalling 2020-2022 iH-45, Realm, and iC-37 recreational vehicles because window adhesive may fail, causing the vent to detach and increasing crash risk.

    Product
    FORETRAVEL — FORETRAVEL IC-37, IH-45, REALM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V785000·2021-10-08

    Forest River Recalls 2021-2022 Entrada Motorhomes Due to Brake Line Wear

    Forest River is recalling 2021-2022 Entrada motorhomes because brake lines may wear against leveling jack brackets, potentially causing brake failure and increasing crash risk.

    Product
    EAST TO WEST — EAST TO WEST ENTRADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V787000·2021-10-08

    Starcraft Transit Bus Recall for Incorrect Emergency Exit Window Labels

    Forest River is recalling 2012-2016 Starcraft transit buses because rear emergency exit window labels are misplaced and incomplete, potentially delaying evacuation.

    Product
    STARCRAFT BUS — STARCRAFT BUS TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V786000·2021-10-08

    Star Trans School Bus Recall for Incorrect Emergency Exit Window Labels

    Forest River is recalling 2014-2016 Star Trans school buses because rear emergency exit window labels are misplaced and incomplete, potentially delaying evacuation.

    Product
    STARTRANS — STARTRANS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·037-2021·2021-10-08

    Crider Foods Recalls Canned Beef With Gravy Due to Lead Contamination

    Crider Foods is recalling approximately 684,774 pounds of canned beef with gravy products due to possible unsafe levels of lead from a spice mix.

    Product
    Crider, Inc. — Crider Foods Recalls Canned Beef With Gravy Products Due to Possible Unsafe Levels of Lead From Outside Source
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V782000·2021-10-07

    GM Recalls Buick Enclave and Chevrolet Traverse for Air Bag Defect

    General Motors is recalling 2008-2017 Buick Enclave and 2013-2017 Chevrolet Traverse vehicles because the driver's air bag inflator may explode during deployment.

    Product
    BUICK — BUICK, CHEVROLET ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide