State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38751–38775 of 73916

HighFDA (Devices)·Z-1528-2018·2018-05-02
EEA Hemorrhoid Stapler Recalled for Potential Welding Defect
FDA is recalling EEA Hemorrhoid and Prolapse Stapler Sets due to a potential welding defect that could cause bleeding or anastomotic leak.
Product
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM, Product Number HEM3348, GTIN Number 1 - 10884521047563, GTIN Number 2 - 20884521047560 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1465-2018·2018-05-02
Zimmer Biomet Recalls Humeral Guide Wires Due to Packaging Seal Failure
Zimmer Biomet is recalling 19,483 M/DN Intramedullary Fixation Humeral Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Product
M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Diameter 70 cm Length Single Use Only; Item Number: 00-2255-025-00
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E029000·2018-05-02
FiTech Fuel Injection Systems Recalled for Fuel Leak Fire Risk
Fuel Injection Technology is recalling Summit Racing Max 500-EFI systems because fuel injector O-rings may leak, increasing fire risk.
Product
FUEL SYSTEM, GASOLINE:FUEL INJECTION SYSTEM recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1128-2018·2018-05-02
Maharaja Food Importers Recalls Jack Fruit for Undeclared Milk Allergen
Maharaja Food Importers is recalling ELA ADA (Jack Fruit) because the label lists ghee but fails to declare milk, a major allergen.
Product
ELA ADA (JACK FRUIT), UPC: 8 70400 00085 2
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1513-2018·2018-05-02
BioFire FilmArray BCID Panel Recalled for False Positive Proteus Results
BioFire Diagnostics is recalling the FilmArray BCID Panel because it may produce false positive Proteus results when used with specific BD BACTEC blood culture bottles.
Product
FilmArray BCID Panel (Blood Culture Identification Panel), Catalog numbers RFIT-ASY-0126 (30 test kit) and RFIT-ASY-0127 (6 test kit), when used with all lots of BD BACTEC Blood Culture Bottles, Catalog numbers 442020, 442021, 442023, 442192, 442265, 442194, 442022, 442193…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2018·2018-05-02
Synthes Stem Extractor Recalled Due to Potential Screw Breakage
Synthes, Inc. is recalling 31 Stem Extractor f/Guide Bar units because the connection screw may break during use.
Product
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1131-2018·2018-05-02
Frozen Parotta Recalled for Undeclared Milk Allergen
Maharaja Food Importers is recalling frozen Parotta products because the label lists ghee but fails to declare milk, a major allergen.
Product
Parotta Family Pack, UPC: 8 70400 00084 5, Frozen; and Small Parotta, UPC: 870400000012, Frozen
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1509-2018·2018-05-02
Stryker T4 Zipper Toga Recall Due to Material Separation Risk
Stryker is recalling T4 Zipper Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Zipper Toga, X-Large; Catalog number: 0400-850-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1527-2018·2018-05-02
Recall of EEA Hemorrhoid and Prolapse Stapler Sets Due to Welding Defect
Covidien LLC is recalling EEA Hemorrhoid and Prolapse Stapler Sets because a defective staple guide may cause bleeding or anastomotic leak during surgery.
Product
EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 - 10884521047518, GTIN Number 2 - 20884521047515 Product Usage: The EEA Hemorrhoid and prolapse stapler set with DST Series Technology (instrument) is designed…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1506-2018·2018-05-02
Stryker T4 Zipper Toga Sterile Garment Recall for Layer Separation
Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Zipper Toga, (L/XL); Catalog Number: 0400-820-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0717-2018·2018-05-02
Coastal Meds Recalls Cyanocobalamin Injectable Due to Particulate Matter
Coastal Meds, LLC. is recalling 745 vials of Cyanocobalamin Injectable due to the presence of unknown particulate matter.
Product
CYANOCOBALAMIN Injectable-30 mL MDV. Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1132-2018·2018-05-02
MMRF Ela Ada Jaggery Recalled for Undeclared Milk Allergen
Maharaja Food Importers is recalling frozen MMRF Ela Ada Jaggery because the label lists ghee but fails to declare milk, a major allergen.
Product
MMRF Ela Ada Jaggery, UPC: 870400000067, Frozen
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1508-2018·2018-05-02
Stryker T4 Zipper Toga Sterile Garments Recalled for Layer Separation
Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T4 Zipper Toga, Regular; Catalog number: 0400-830-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1470-2018·2018-05-02
Zimmer Biomet Recalls ZMS Intramedullary Fixation Smooth Guide Wires
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.
Product
ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter, 100 cm Length; Item Number: 47-2237-037-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2018·2018-05-02
Stryker T4 Pullover Toga Recalled for Potential Material Separation
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T4 Pullover Toga, L/XL; Catalog Number: 0400-720-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18148·2018-05-02
Carter's Recalls Children's Cardigan Sets Due to Choking Hazard
Carter's is recalling 3-piece penguin cardigan sets because the toggle button can detach, posing a choking hazard to young children.
Product
3-piece penguin cardigan sets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1504-2018·2018-05-02
Stryker Recalls T4 Pullover Toga Due to Material Separation Risk
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a potential risk of exposure to contaminants.
Product
T4 Pullover Toga, X-Large; Catalog Number: 0400-770-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0720-2018·2018-05-02
Coastal Meds Recalls LIPO-B Injectable Due to Particulate Matter
Coastal Meds, LLC. is recalling LIPO-B Injectable-30 mL vials due to the presence of unknown particulate matter.
Product
LIPO-B Injectable-30 mL MDV Coastal Meds LLC 1759 Medical Park Dr., Ste C Bioloxi, MS 39532
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1502-2018·2018-05-02
Stryker T4 Pullover Toga Recall Due to Layer Separation Risk
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Product
T4 Pullover Toga, Regular ; Catalog Number: 0400-750-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1463-2018·2018-05-02
Integra LifeSciences Recalls Humeral Stem Trials for Breakage Risk
Integra LifeSciences is recalling 1,619 humeral stem trials for the Titan Modular Shoulder System because they may break during surgery.
Product
The humeral stems trials are packaged in a kit for Titan Modular Shoulder System under the following labeling: Catalog Number Product Description TRL092002506 Humeral Stem Trial, 6mm TRL092002507 Humeral Stem Trial, 7mm TRL092002508 Humeral Stem Trial, 8mm TRL092002509…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1503-2018·2018-05-02
Stryker T4 Pullover Toga Recall Due to Layer Separation
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, creating a risk of exposure to contaminants.
Product
T4 Pullover Toga, Large; Catalog Number: 0400-760-000 Sterile personal protection garment
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1466-2018·2018-05-02
Zimmer Biomet Recalls Humeral Guide Wire Ball Tips Due to Packaging Seal Failure
Zimmer Biomet is recalling Humeral Guide Wire Ball Tips because the sterile packaging seal may fail, potentially compromising the device's sterility.
Product
Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length; Item Number: 47-2255-008-00
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1533-2018·2018-05-02
BD Vacutainer Blood Collection Set Recalled for Sterility Assurance Failure
Becton Dickinson is recalling BD Vacutainer Ultra Touch Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Product
BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12. Catalog no 367364
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18E030000·2018-05-02
Ivolution Recalls IV2 HY-811 Motorcycle Helmets for Vision Blockage
Ivolution Sports Inc. is recalling IV2 HY-811 motorcycle helmets because they may block peripheral vision, increasing crash risk.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1133-2018·2018-05-02
Maharaja Food Importers Recalls Whole Wheat Parotta for Undeclared Milk
Maharaja Food Importers, Inc. is recalling Whole Wheat Parotta because the label lists ghee but fails to declare milk as an ingredient.
Product
WHOLE WHEAT PAROTTA, UPC: 8 70400 00092 0
Category
Food
Distribution
Distributed nationwide