State

US Virgin Islands product recalls

73,827 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55626–55650 of 74005

HighFDA (Devices)·Z-0979-2015·2015-01-21
Philips CT Systems Recalled for Improper Vertical Motor Assembly
Philips is recalling Brilliance and Ingenuity CT systems because improper assembly of the vertical motor/brake system may lead to uncommanded vertical motion.
Product
Various Brilliance and Ingenuity Computed Tomography X-ray systems; one unit per package Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. This device may include…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15061·2015-01-21
Mean Green Cleaner and Degreaser Recalled for Ammonia Mislabeling
CR Brands is recalling Mean Green cleaner and degreaser products because they may contain ammonia despite labels stating otherwise, posing a chemical hazard.
Product
Mean Green® Super Strength Cleaner & Degreaser and Mean Green® Industrial Strength Cleaner & Degreaser
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2015·2015-01-21
Becton Dickinson Recalls Columbia Agar with 5% Sheep Blood Due to Listeria
Becton Dickinson & Co. is recalling Columbia Agar with 5% Sheep Blood due to low-level Listeria monocytogenes contamination. The product is a non-sterile culture medium distributed worldwide.
Product
Columbia Agar with 5% Sheep Blood Columbia Agar with 5% Sheep Blood is a general purpose culture medium used for the growth and recovery of fastidious microbial species.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2015·2015-01-21
Becton Dickinson Recalls CDC Anaerobe Agar Due to Listeria Contamination
Becton Dickinson is recalling CDC Anaerobe 5% Sheep Blood Agar due to low-level Listeria monocytogenes contamination. The affected non-sterile media were distributed worldwide.
Product
CDC Anaerobe 5% Sheep Blood Agar CDC Anaerobe 5% Sheep Blood Agar is an enriched, nonselective culture medium particularly useful or the isolation and cultivation of obligate anaerobes from clinical specimens. It supports the growth of a wide variety of obligately anaerobic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0960-2015·2015-01-21
Siemens Symbia CT Systems Recalled for Internal Component Damage
Siemens Medical Solutions is recalling 295 Symbia T and T2 CT systems because a component may come loose and damage the equipment.
Product
Symbia T and Symbia T2 computer tomography systems. These systems are used to perform SPECT, CT, and SPECT + CT scans and imaging studies.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0947-2015·2015-01-21
Phadia 1000 Instrument Recalled for Rack Sequencing Error
Phadia US Inc is recalling 146 Phadia 1000 instruments due to a software error that may cause sample ID and test result mismatches.
Product
Phadia 1000 Instrument (introduced as UniCAP 1000), Article number: 12-3800-01 (All instrument software versions since launch in 2003); Multiple ImmunoCAP assays for Allergen Testing, FDA Cleared for use on Phadia 1000 instrument with IU statement-see attachments. Software…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0981-2015·2015-01-21
Straumann Dental Implant Drill Set Recalled for Incorrect Drill
Straumann USA is recalling dental implant drill sets that may contain incorrect drills. The recall covers 362 pieces distributed nationwide and internationally.
Product
Drill set long, drill stop compatible for 4.8mm diameter implant, Article Number 040.447S Endosseous dental implant drill set.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0965-2015·2015-01-21
Biocare Medical Recalls MUM-1 Antibody Lots Due to Staining Intensity Issues
Biocare Medical is recalling three lots of MUM-1 antibody because staining intensity drops over time, potentially affecting diagnostic accuracy.
Product
MUM-1 (Multiple myeloma oncogene-1), catalog number PRM352 AA; Product Usage: For In Vitro Diagnostic Use. This antibody may be used as a tool for the identification and the sub classification of lymphoid malignancies : Multiple myeloma oncogene-1 (MUM-1) is a protein…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0969-2015·2015-01-21
Ortho VITROS 5600 System Recalled for Software Calibration Error
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because software may fail to identify expired calibrations.
Product
VITROS 5600 Integrated System, Catalog Number 6802413, IVD --- Ortho Clinical Diagnostics. For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products Slides, VITROS…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0968-2015·2015-01-21
Ortho VITROS 4600 Chemistry System Recalled for Software Calibration Error
Ortho-Clinical Diagnostics is recalling VITROS 4600 Chemistry Systems because software versions 3.1 and below may fail to identify expired calibrations.
Product
VITROS 4600 Chemistry System (VITROS 5,1 FS System family member), Catalog Number 6802445, IVD --- Ortho Clinical Diagnostics. The VITROS 4600 Chemistry System is intended for use in the in vitro quantitative measurement of a variety of analytes of clinical interest, using…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0988-2015·2015-01-21
Ziemer Femto LDV Z-Generation Lasers Recalled for Missing Starter Kits
Ziemer USA Inc. is recalling 26 Femto LDV Z-Generation femtosecond surgical lasers because they were not shipped with the required Starter Kits.
Product
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0784-2015·2015-01-21
NatureBox Sweet Blueberry Almonds Recalled for Missing Soy Labeling
NatureBox, Inc. is recalling Sweet Blueberry Almonds because the product label failed to list soy lecithin, an ingredient included in the recipe.
Product
Sweet Blueberry Almonds - Blueberry Flavored Almonds. Ingredients: Almonds, Sugar, Natural Flavor, Vegetable Color (Red Cabbage Juice Extract), Beet Juice Concentrate. May also contain other tree nuts, peanuts, milk, wheat, egg. Packaged in the following configuration: 4…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0967-2015·2015-01-21
Ortho VITROS 3600 Immunodiagnostic System Recalled for Software Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems because software versions 3.1 and below may fail to identify expired calibrations.
Product
VITROS 3600 Immunodiagnostic System, Catalog Number 6802783, IVD --- Ortho Clinical Diagnostics. For use in the in vitro quantitative, semi-quantitative and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0986-2015·2015-01-21
Stryker Recalls SurgiCounter Charging Cradles Due to Charging Defects
Stryker is recalling 3,625 SurgiCounter Charging Cradles because they may fail to charge the scanner or download data after surgical procedures.
Product
The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging Cradles are designed to be used with the SurgiCounter and are part of the SurgiCount Safety-Sponge System. The SurgiCount Safety-Sponge System is indicated for use in counting and recording the number…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V016000·2015-01-20
Porsche Recalls 2011-2012 Hybrid Models Due to Fuel Leak Risk
Porsche is recalling 2011-2012 Cayenne S Hybrid and 2012 Panamera S Hybrid vehicles because the fuel injection system may leak, increasing fire risk.
Product
PORSCHE — PORSCHE PANAMERA S HYBRID, CAYENNE S HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V021000·2015-01-20
Polar Tank Trailer Recall for Potential Brake Fire Risk
Polar Tank Trailer is recalling 2015 ATB6, APX0, and SRJH trailers due to a parking brake actuator defect that may cause brake drag and fire.
Product
POLAR TANK — POLAR TANK ATB6 TRAILER, APX0 TRAILER, SRJH TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V020000·2015-01-20
Polaris Recalls 2015 Slingshot Motorcycles Due to Roll Hoop Defect
Polaris is recalling 2015 Slingshot and Slingshot SL motorcycles because roll hoops may not meet hardness specifications, increasing injury risk in rollovers.
Product
POLARIS — POLARIS SLINGSHOT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V017000·2015-01-20
Jayco Eagle Fifth Wheel Trailers Recalled for Incorrect Tire Labeling
Jayco is recalling 2015 Eagle 30.5 BHLT fifth wheel trailers because the tire labels list incorrect tire sizes. Owners should contact Jayco to receive corrected labels to prevent potential tire failure.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V019000·2015-01-20
Volkswagen Recalls Audi and VW Models for Fuel Leak Fire Risk
Volkswagen is recalling 26,008 Audi and Volkswagen vehicles because a fuel leak in the injection system could cause a fire.
Product
AUDI — AUDI, VOLKSWAGEN A7, A6, TOUAREG HYBRID, S4
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V018000·2015-01-20
Frontline Mobile Medical Units Recalled for Wheelchair Lift Defect
Frontline Communications is recalling 2007-2011 Mobile Medical Units because wheelchair lift platform side plates may crack, posing an injury risk.
Product
FRONTLINE COMMUNICATIONS — FRONTLINE COMMUNICATIONS MOBILE MEDICAL UNIT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15E001000·2015-01-20
Tucker Rocky Recalls Speed and Strength SS500DVD Motorcycle Helmets
Tucker Rocky is recalling specific Speed and Strength SS500DVD motorcycle helmets because they fail to meet federal safety standards, increasing the risk of serious injury in a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
CriticalUSDA FSIS·014-2015·2015-01-17
La Guadalupana Recalls Chicken Tamales Lacking Required Safety Plans
La Guadalupana Wholesale is recalling chicken tamales produced without required HACCP and Listeria programs. No illnesses have been reported.
Product
La Guadalupana — Illinois Firm Recalls Chicken Products Produced Without Adequate Ready-To-Eat HACCP Plan and a Listeria Monocytogenes Program
Category
Food
Distribution
Distributed nationwide
CriticalUSDA FSIS·016-2015·2015-01-17
Sentry Food Solutions Recalls Chicken and Beef Products for Undeclared Peanuts
Sentry Food Solutions is recalling approximately 14,130 pounds of chicken and beef products because they may contain undeclared peanuts.
Product
Georgia Firm Recalls Chicken and Beef Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·015-2015·2015-01-17
Kalle USA Recalls Pork Products Produced Without Inspection
Kalle USA is recalling approximately 168,473 pounds of dehydrated pork products that were not presented for U.S. inspection. No adverse reactions have been reported.
Product
Illinois Firm Recalls Pork Products Produced Without Benefit of Inspection
Category
Food
Distribution
Distributed nationwide
SevereUSDA FSIS·014-2015(Original)·2015-01-17
La Guadalupana Recalls Chicken Tamales Lacking Required Safety Plans
La Guadalupana Wholesale is recalling 8,856 pounds of chicken tamales because they were produced without a required HACCP plan or Listeria program.
Product
La Guadalupana — Illinois Firm Recalls Chicken Products Produced Without Adequate Ready-To-Eat HACCP Plan and a Listeria Monocytogenes Program
Category
Food
Distribution
Distributed nationwide