State

US Virgin Islands product recalls

73,104 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: 30
Most recent: 2026-09-23

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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12076–12100 of 73281

HighFDA (Drugs)·D-0378-2024·2024-03-20
TRP Natural Eyes Dryness Relief Eye Drops Recalled for Lack of Sterility Assurance
Optikem International, Inc. is recalling TRP Natural Eyes Dryness Relief eye drops due to lack of assurance of sterility. The product was distributed nationwide in the USA.
Product
TRP Natural Eyes Dryness Relief, Sterile Eye Drops, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-178-15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1291-2024·2024-03-20
CLEARLINK Solution Set Adapter recalled for potential drip chamber leaks
Baxter Healthcare recalls CLEARLINK Non-DEHP Solution Set Luer Lock Adapters due to potential leaks in the drip chamber. The recall affects 26,592 units distributed nationwide.
Product
CLEARLINK Non-DEHP Solution Set Luer Lock Adapter, Product Code 2R8401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0383-2024·2024-03-20
TRP Natural Eyes Red Eye Relief eye drops recalled for sterility concerns
The FDA is recalling 106,704 bottles of TRP Natural Eyes Red Eye Relief eye drops due to lack of sterility assurance. Consumers should stop using the product and contact a healthcare provider if they experience eye irritation or infection.
Product
TRP Natural Eyes Red Eye Relief, Sterile Eye Drops, Homeopathic, 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-158-15.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1289-2024·2024-03-20
STERIS Boot Assembly, Traction Device Recalled Due to Locking Pin Detachment Risk
Baxter Healthcare is recalling STERIS Boot Assembly traction devices due to an incorrectly oriented locking pin that may cause the boot to detach during surgery, posing patient safety risks.
Product
STERIS Boot Assembly, Traction Device, OT 1000, Part Number REF 10009192
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1297-2024·2024-03-20
Hip prosthesis labeling guidance issue affects 34 units
The FDA is advising on label interpretation for the SPII Model Lubinus hip prosthesis stem to prevent confusion during surgery. Two complaints prompted additional guidance on carton label size and type columns.
Product
SPII Model Lubinus, Hip Prosthesis Stem XL Neck, cemented
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0368-2024·2024-03-20
Prescription drug Febuxostat recalled due to manufacturing contamination
Sun Pharmaceutical is recalling 47,520 bottles of Febuxostat 40mg tablets nationwide due to microbial contamination found in manufacturing equipment. The FDA classified this as a Class II recall; no illnesses have been reported.
Product
FEBUXOSTAT — FEBUXOSTAT (FEBUXOSTAT)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1296-2024·2024-03-20
Hip Prosthesis Stem Labels Lack Clear Guidance on Size and Type
A hip prosthesis stem was recalled due to ambiguous carton label guidance that could cause incorrect implant selection during surgery. The recall affects 382 units.
Product
SPII Model Lubinus, Hip Prosthesis Stem Standard Neck, cemented
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1283-2024·2024-03-20
Ivenix Infusion System Software Defect May Delay or Cause Incorrect Infusions
Fresenius Kabi recalls Ivenix Infusion System software versions 5.2.1 and 5.2.2 due to two defects that may delay therapy or cause over-infusion. The software fix was deployed to affected units between May and August 2023.
Product
LVP software of the Ivenix Infusion System (IIS); LVP-SW-0004
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1279-2024·2024-03-20
D-Clip Surgical Applier Recalled for Failure to Release During Surgery
FDA has recalled the D-Clip Standard/Mini Applier due to reports that the device failed to release the clip and remained attached during surgical use, creating a risk of surgical complications.
Product
D-Clip Standard/Mini Applier, 230mm bayonet, jaw rigid, double action.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0384-2024·2024-03-20
FDA Recalls HylaTears Lubricant Eye Drops for Sterility Assurance Issue
Optikem International is recalling 46,621 bottles of hyalogic For Dry Eyes, HylaTears Lubricant Eye Drops due to lack of assurance of sterility. The product is distributed nationwide.
Product
hyalogic For Dry Eyes, HylaTears", Lubricant Eye Drops, 0.67 FL OZ (20mL) bottle, Manufactured for hyalogic, 610 NW Platte Valley Dr., Riverside, MO 64150
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0377-2024·2024-03-20
Eye Drops Recall: TRP Eye Twitching Relief Lacks Sterility Assurance
TRP Eye Twitching Relief sterile eye drops are being recalled nationwide because the manufacturer cannot assure the product meets sterility requirements. The affected lot (C303, expiring 07-27-2025) was distributed in the USA.
Product
TRP Eye Twitching Relief, Sterile Eye Drops, Homeopathic 0.33 FL OZ (10 mL), Manufactured for TRP Company, Inc, 1575 Delucchi Lane, Suite # 208, Reno, NV, NDC # 17312-040-15.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1282-2024·2024-03-20
Infusion Pump Software Defect Causes Incorrect Alarm and Therapy Delay
Fresenius Kabi is recalling software versions 5.0.1 and earlier of the Ivenix Infusion System due to a software defect that may cause an incorrect pump alarm, potentially delaying therapy. The defect was resolved in software version 5.2.1, released in September 2022.
Product
LVP software of the Ivenix Infusion System (IIS), LVP-SW-0004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1294-2024·2024-03-20
BVI Visitec Irrigation Handle lacks manufacturing and expiration dates
Beaver Visitec International is recalling 3,000 BVI Visitec Irrigation Handles because the pack and pouch labels are missing manufacturing and expiration date information.
Product
BVI Visitec Irrigation Handle (20/SP)- Intended to be fit with a cannula for irrigation of the eye Catalog Number: 581012
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1298-2024·2024-03-20
Hip prosthesis labeling clarification needed to prevent surgical confusion
Waldemar Link is clarifying labeling on 153 hip prosthesis units after complaints about ambiguous Size and Type information. The guidance aims to prevent potential misinterpretation during surgery.
Product
SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0386-2024·2024-03-20
Broncochem Cold & Flu Syrup Kids Recalled Due to Stability Testing Failures
Global Corporation is recalling Broncochem Cold & Flu Syrup Kids (120 mL bottles) nationwide due to stability testing failures in active pharmaceutical ingredients.
Product
Broncochem Cold & Flu Syrup Kids (acetaminophen, guaifenesin, phenylephrine HCl), packaged in 120 mL bottles, Made in Dominican Republic Exclusively for Global Corporation Inc, Boca Raton, FL 33187 USA, NDC 65131-098-44
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0387-2024·2024-03-20
FDA Recalls Broncochem Cold & Tea Nationwide for Stability Failures
Global Corporation is recalling Broncochem Cold & Tea nationwide due to stability testing failures in the active ingredients. No illnesses or injuries have been reported.
Product
BRONCOCHEM — BRONCOCHEM (ACETAMINOPHEN-PHENYLEPHRINE HYDROCHLORIDE-CHLORPHENIRAMINE MALEATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1287-2024·2024-03-20
Aneurysm clips recalled due to incorrect blue coloring
Peter Lazic Gmbh is recalling 170 L-Aneurysm Clip TITANIUM Paddle-Clips distributed in Maine due to incorrect blue coloring instead of blank.
Product
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Sterile
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0369-2024·2024-03-20
Febuxostat tablets recalled due to microbial contamination in manufacturing
Sun Pharmaceutical is recalling 7,488 bottles of Febuxostat 80mg tablets nationwide due to microbial contamination found in manufacturing equipment. No illnesses have been reported.
Product
FEBUXOSTAT — FEBUXOSTAT (FEBUXOSTAT)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1288-2024·2024-03-20
Aneurysm clips recalled due to incorrect paddle coloring
Peter Lazic Gmbh is recalling 51 titanium aneurysm clip paddle clips because the clips are colored blue when they should be blank.
Product
L-Aneurysm Clip TITANIUM Paddle-Clip, permanent, 11 mm straight, Non-Sterile
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V211000·2024-03-19
Titan Bus Recalls Chevrolet Express 3500 Vehicles for Missing Certification Placard
Titan Bus is recalling 2018-2021 Chevrolet Express 3500 vehicles because the federal certification placard may be missing, which could lead to unintentional overloading and increased crash risk.
Product
TITAN BUS — TITAN BUS CHEVROLET EXPRESS 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V209000·2024-03-19
2024 Alfa Romeo Tonale vehicles with missing tire and rim label information
Chrysler is recalling certain 2024 Alfa Romeo Tonale vehicles because the manufacturer label is missing tire rim and tire size information, which could lead to incorrect wheel installation and increase crash risk.
Product
DODGE — DODGE, ALFA ROMEO HORNET, TONALE PHEV
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V210000·2024-03-19
Cruiser Avenir Trailers Recalled for Missing Tire Certification Labels
Cruiser RV is recalling 2023-2024 Avenir trailers because Federal Certification labels lack tire size and PSI data, potentially leading to incorrect tire installation or inflation.
Product
CRUISER — CRUISER AVENIR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V212000·2024-03-19
2023–2024 Jayco and Entegra Motorhomes Rearview Camera Failure Recall
Jayco, Inc. is recalling certain 2023–2024 Jayco Solstice and Entegra Expanse motorhomes built on Ford chassis because the rearview camera may not display an image when in reverse, reducing rear visibility and increasing crash risk.
Product
JAYCO — JAYCO, ENTEGRA SOLSTICE LI, SOLSTICE, EXPANSE LI, EXPANSE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V203000·2024-03-17
2021–2023 Nova Bus LFS Buses Power Cable Nut Fire Risk
Nova Bus is recalling certain 2021–2023 LFS buses because the alternator power cable nut may not have been tightened properly, increasing the risk of electrical arcing and fire.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V207000·2024-03-15
Mercedes-Benz Recalls Vehicles Due to 48-Volt Ground Connection Fire Risk
Mercedes-Benz is recalling specific 2019-2024 models because a 48-Volt ground connection may overheat, increasing the risk of a fire.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH AMG GLE53, AMG GLE63 S 4MATIC+, GLS 600, GLS 600 4MATIC
Category
Vehicle
Distribution
Distributed nationwide