The Recall Desk

State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54626–54650 of 74002

  • SevereNHTSA·15V242000·2015-04-22

    Navistar Recalls 2014-2015 IC Bus AE School Buses for Fire Risk

    Navistar is recalling 113 model year 2014-2015 IC Bus AE school buses because an electrical issue could cause the HVAC system to overheat and start a fire.

    Product
    IC BUS — IC BUS AE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V239000·2015-04-22

    Polaris Recalls 2009-2010 GEM eLXD Vehicles Due to Frame Weld Cracks

    Polaris is recalling 2009-2010 GEM eLXD hybrid electric vehicles because frame welds may crack, potentially causing the frame to fall and stop the vehicle suddenly.

    Product
    GEM — GEM ELXD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V240000·2015-04-22

    Toyota Recalls 2015 Sienna Minivans Due to Trim Panel Clip Defect

    Toyota is recalling 387 model year 2015 Sienna minivans because a reused trim panel clip may detach during airbag deployment, posing an injury risk to occupants.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1442-2015·2015-04-22

    Baylis Medical Recalls ProTrack Microcatheter Due to Circumferential Shaft Defects

    Baylis Medical Corp is recalling two lots of ProTrack Microcatheters due to potential circumferential defects along the device shaft.

    Product
    ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2015·2015-04-22

    Bard PICC and Dialysis Catheter Kits Recalled for Scalpel Injury Risk

    Bard Access Systems is recalling PICC and dialysis catheter kits containing Safe-Cut Safety Scalpels due to the potential for inadvertent scalpel stick injuries.

    Product
    Bard Peripherally Inserted Central Catheter (PICC) and Dialysis catheter kits containing Safe-Cut Safety Scalpels.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15120·2015-04-22

    Shark Vacuum Cleaners Recalled by Euro-Pro Due to Shock Hazard

    Euro-Pro is recalling Shark vacuum cleaners because the aluminum wand can disconnect and remain energized, posing an electric shock risk.

    Product
    Shark Powered Rotator Lift-Away vacuum cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1954-2015·2015-04-22

    ProThera Recalls Ther-Biotic Probiotic Supplements Due to Glass Shards

    ProThera, Inc. is recalling three lots of Ther-Biotic Children's Chewable probiotic supplements because shards of blue glass were found in the bottles.

    Product
    Klaire Labs Ther-Biotic Children's Chewable 125+ Billion CFU's Multi-Species Probiotic Supplement 60 Chewable Capsules. UPC 7 09616 01247 5 Manufactured by ProThera Inc . Klaire Labs is a division of ProThera, Reno, NV.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1447-2015·2015-04-22

    Bard Monopty Disposable Core Biopsy Instruments Recalled for Activation Issues

    Bard Peripheral Vascular is recalling specific Bard Monopty Disposable Core Biopsy Instruments and Kits due to potential activation-related issues.

    Product
    Bard Monopty Disposable Core Biopsy Instruments and Kits, Monopty 14g x 16cm (22mm), Product Code: 121416; Monopty Biopsy, Product Code: 000441; Monopty 14g x 10cm (22mm), Product Code: 121410; Monopty 14g x 10cm (11mm), Product Code: 211410. The BARD MONOPTY Disposable Core…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1953-2015·2015-04-22

    ProThera Recalls Ther-Biotic Probiotic Supplements Due to Glass Shards

    ProThera, Inc. is recalling specific lots of Klaire Labs Ther-Biotic FACTOR 6 probiotic supplements because blue glass shards were found in the bottles.

    Product
    Klaire Labs Ther-Biotic FACTOR 6 100+ Billion CFU's Multi-Species Probiotic Supplement 60 Vegetarian Capsules. UPC 7 09616 01248 2 Manufactured by ProThera Inc . Klaire Labs is a division of ProThera, Reno, NV.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2015·2015-04-22

    CooperSurgical Recalls Wallach LL 100 Cryosurgical Units Due to Gas Line Burst Risk

    CooperSurgical is recalling 255 Wallach LL 100 cryosurgical units because an internal gas line may malfunction and burst under pressure.

    Product
    WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number 900019-70; LL100 Multi Tip W/TC - Part Number: 900629; LL100 - CO2 - Part Number 900162
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1955-2015·2015-04-22

    Kraft Macaroni and Cheese Recalled for Potential Metal Contamination

    Kraft Foods Group Inc. is voluntarily recalling boxed Macaroni & Cheese dinners because they may contain metal pieces.

    Product
    Kraft Macaroni & Cheese Boxed Dinner Original Flavor, 7.25oz.,packaged in blue and yellow cardboard box. There are four different package types affected by this recall: 1) single 7.25 oz boxes, 3-pack box of 7.25 oz boxes, 4-pack shrink wrap of 7.25 oz boxes, and 5-pack shrink…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1435-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Issue

    Nobel Biocare is recalling 216 units of NobelReplace CC PMC NP dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC PMC NP 3.5x11.5mm, Article No. 37287.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1416-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 24 units of Replace Select Tapered TiU NP 3.5x16mm dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    Replace Select Tapered TiU NP 3.5x16mm, Article No. 29403. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1432-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Issue

    Nobel Biocare is recalling 56 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC RP 5.0x8mm, Article No. 36710.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1439-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 53 units of NobelReplace CC PMC RP 5.0x10mm dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC PMC RP 5.0x10mm, Article No. 37296.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1446-2015·2015-04-22

    Biomet Recalls Low Profile Non-Locking Screws Due to Anodizing Error

    Biomet is recalling 45 Low Profile Non-Locking Screws because they were anodized green instead of the required gold color.

    Product
    LOW PROFILE NON-LOCK SCREW; 2.7mm x 22 mm; REF 131227222; LOT RM105E. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1420-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Contamination

    Nobel Biocare is recalling 74 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NOBELREPLACE Tapered Groovy RP 4.3x10mm, Article No. 32216. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1421-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 7 dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NOBELREPLACE Tapered Groovy 6.0 6x8mm, Article No. 32223. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0488-2015·2015-04-22

    Actavis Recalls Cartia XT Capsules Due to Aluminum Residue on Exterior

    Actavis is recalling 2,628 bottles of Cartia XT capsules because fine aluminum residue was found on the exterior of the capsule shells.

    Product
    Cartia XT (diltiazem HCl extended-release capsules, USP), Once-A-Day Dosage, 300 mg, 90-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA --- NDC 62037-0600-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1414-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 131 units of Replace Select Tapered TiU NP dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    Replace Select Tapered TiU NP 3.5x10mm, Article No. 29401. Nobel Biocare's Dental Implants are root-form endosseous implants intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as an artificial tooth, in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1440-2015·2015-04-22

    Nobel Biocare Recalls Dental Implants Due to Packaging Material Contamination

    Nobel Biocare is recalling 38 units of NobelReplace CC PMC RP 5.0x13mm dental implants because packaging material may leave a sticky substance on the implant surfaces.

    Product
    NobelReplace CC PMC RP 5.0x13mm, Article No. 37298.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1445-2015·2015-04-22

    Siemens Artis Q and Q zen Angiography Systems Recalled for Electrical Connection

    Siemens is recalling 139 Artis Q and Q zen angiography systems nationwide because an electrical connection in the equipment cabinet may not be installed correctly.

    Product
    Artis Q/ Q zen systems; Artis Q/ Q zen systems are dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed include cardiac…
    Category
    Medical Device
    Distribution
    Distributed nationwide