State

US Virgin Islands product recalls

73,100 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 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11476–11500 of 73277

HighFDA (Drugs)·D-0476-2024·2024-05-08
FDA Issues Nationwide Recall of Subpotent Ophthalmic Eye Drops
The FDA is recalling 3,320 bottles of compounded ophthalmic solution due to subpotency. The affected product does not contain adequate amounts of active medication.
Product
Prednisolone Sodium Phosphate-Moxifloxacin-Bromfenac Sterile Ophthalmic Solution 1%, 0.5%, 0.075%, 8mL, Compounded By: Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B Ledgewood, NJ 07852, NDC 71384-340-08
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2024·2024-05-08
Unsterilized Jackson-Pratt surgical drain kits recalled by Cardinal Health
Cardinal Health recalls Jackson-Pratt 3-Spring Reservoir Kits because specific lots were shipped before sterilization. Unsterilized surgical devices pose risk of infection.
Product
Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 10Fr., REF SU130-402D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2024·2024-05-08
Radiation therapy planning system doses may be calculated incorrectly
Certain versions of RayStation radiation therapy planning software may incorrectly report dose-related parameters, potentially affecting treatment calculations. The manufacturer recommends verification of affected systems.
Product
RayStation 12.0.0.932, 12.1.0.1221, 12.0.3.68, 12.0.4.12 &12.3.0.119. Radiation Therapy Treatment Planning System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1729-2024·2024-05-08
Zimmer Distal Lateral Fibular Plate Recall Due to Locking Thread Defect
Zimmer recalls certain ZPLP Distal Lateral Fibular Plates due to thread form defects in locking holes that may prevent proper screw fixation. Affected devices may lose fixation, potentially delaying surgery or requiring additional intervention.
Product
ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 00-2357-018-10
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2024·2024-05-08
Johnson & Johnson Irrigation Sleeve Recalled for Manufacturing Defect
Johnson & Johnson is recalling 3,428 reusable irrigation sleeves due to manufacturing defects that could impair cooling during eye surgery, potentially causing anterior chamber instability and patient harm.
Product
Johnson & Johnson VISION Reusable LAMINAR High Flow Irrigation Sleeve and Test Chamber 21 Gauge REF OPOHF21L The irrigation sleeve is a device intended to direct irrigation solution across the shaft of a phacoemulsification tip, allowing the solution to enter the eye during…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1737-2024·2024-05-08
Jackson-Pratt 3-Spring Reservoir Kit Recalled Due to Non-Sterile Shipment
Cardinal Health is recalling Jackson-Pratt 3-Spring Reservoir Kits after shipping specific lots before sterilization. The affected devices pose an infection risk if used without proper sterilization.
Product
Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain, 400mL, 15Fr., REF SU130-403D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2024·2024-05-08
RayStation 7.0.0.19 radiation therapy planning software recalled for dose calculation error
RayStation 7.0.0.19, a radiation therapy treatment planning system, is being recalled due to potential source-to-surface distance (SSD) calculation errors that could affect radiation dose accuracy. The recall affects 14 units distributed worldwide.
Product
RayStation 7.0.0.19. Radiation Therapy Treatment Planning System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1748-2024·2024-05-08
Radiation Therapy Planning System May Calculate Skin Surface Distance Incorrectly
RayStation radiation therapy planning software versions 11.0.0.951, 11.0.1.29, 11.0.3.116, and 11.0.4.15 may calculate skin surface distance (SSD) values incorrectly, potentially affecting dose calculations. Affected software has been distributed worldwide.
Product
RayStation 11.0.0.951, 11.0.1.29, 11.0.3.116 & 11.0.4.15. Radiation Therapy Treatment Planning System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1717-2024·2024-05-08
Zimmer Periarticular Locking Plate recalled for improper screw mating defect
Zimmer, Inc. is recalling the ZPLP Distal Lateral Fibular Plate due to a thread form defect that may prevent locking screws from properly mating with the plate, potentially causing surgical delays or loss of fixation.
Product
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-08
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1709-2024·2024-05-08
Zimmer Distal Lateral Fibular Plate may fail to lock screws securely
Zimmer's Distal Lateral Fibular Plate has threading defects that may prevent screws from locking properly. The defect could go unnoticed during surgery and cause loss of fixation.
Product
ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Right, 4 Holes, 80 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-017-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1742-2024·2024-05-08
Radiation therapy planning system may report overly high skin surface doses
RayStation versions 8.0.0.61 and 8.0.1.10 are subject to a Class II FDA recall due to a potential for calculated skin surface doses to be reported as too high. Healthcare facilities using these versions should contact the manufacturer for guidance and a corrective update.
Product
RayStation 8.0.0.61, 8.0.1.10. Radiation Therapy Treatment Planning System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1746-2024·2024-05-08
RayStation Radiation Therapy Planning Software Recalled for Calculation Error
RayStation radiation therapy planning software versions 10.0.0.1154, 10.0.1.52, and 10.0.2.10 have been recalled due to a potential calculation parameter issue that could affect treatment planning. The FDA classified this as a Class II recall affecting 213 units worldwide.
Product
RayStation 10.0.0.1154, 10.0.1.52 & 10.0.2.10. Radiation Therapy Treatment Planning System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1705-2024·2024-05-08
Zirconium oxide dental blocks recalled due to cracking and fracture risk
IVOCLAR VIVADENT is recalling IPS e.max ZirCAD zirconium oxide blocks nationwide because they may develop cracks after sintering that could cause dental restorations to fracture in patients' mouths.
Product
IPS e.max ZirCAD CER/in. Prime A2 C17/5 -A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758438
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1756-2024·2024-05-08
Philips Spectral CT Oncology Imaging System Recall: Laser Reflection Hazard
Philips recalls 12 units of its Spectral CT Oncology Essentials system because a marking laser could reflect off the gantry cover, potentially causing misdiagnosis and incorrect patient treatment.
Product
The Oncology Essentials Package of the Spectral CT imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1704-2024·2024-05-08
Zirconium oxide dental blocks recalled due to cracking risk
IVOCLAR VIVADENT AG is recalling 7,445 units of IPS e.max ZirCAD CER/in. Prime zirconium oxide blocks because they may crack during sintering, potentially causing dental restorations to fracture in patients' mouths.
Product
IPS e.max ZirCAD CER/in. Prime A1 C17/5 - A zirconium oxide block for the fabrication of fixed, full-contour restorations in anterior and posterior teeth. Article Number: 758437
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0478-2024·2024-05-08
Injectable epinephrine-lidocaine recalled for failing potency specification
Imprimis NJOF, LLC is recalling epinephrine-lidocaine injectables nationwide because they failed to meet potency specifications. Patients should contact their healthcare provider regarding affected lots.
Product
Epinephrine-Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL Preservative-Free, 1 mL Single-Use vials, Rx only, Imprimis NJOF, LLC 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852, NDC 71384-640-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0481-2024·2024-05-08
Prescription Valacyclovir Tablets Recalled Due to Missing Imprint
Viatris Inc is recalling 143,230 bottles of Valacyclovir Hydrochloride 500 mg tablets due to missing imprints on some tablets. The recall is nationwide and affects two lot numbers expiring in June 2024 and May 2025.
Product
VALACYCLOVIR HYDROCHLORIDE — VALACYCLOVIR HYDROCHLORIDE (VALACYCLOVIR)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0480-2024·2024-05-08
Fentanyl Injection Bags Recalled Due to Incorrect Barcode Labels
Hikma Injectables USA Inc. has recalled 1,895 bags of Fentanyl 1000mcg/100mL injection (lot CH0324001) due to incorrect barcodes on the product labeling.
Product
Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection, packaged in 100mL bags, Rx only, Compounded by: Hikma Injectables USA Inc. 2 Esterbrook Lane, Cherry Hill, NJ 08003, Distributed by: Hikma Injectables USA Inc. 36 Stults Road, Dayton, NJ 08810, NDC 63037-100-05
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·24V318000·2024-05-07
Winnebago motorhomes recalled for airbag system wiring damage
Winnebago motorhomes are being recalled due to airbag system wiring that can be trapped in the seat mechanism when seats are adjusted. Damaged wires could prevent the airbags from deploying in a crash.
Product
WINNEBAGO — WINNEBAGO ADVENTURE WAGON, VITA, REVEL, PORTO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E037000·2024-05-06
AFCO Legend Revo Arc Remote Reservoir FLH Kits Recall for Suspension Brackets
AFCO Performance Group is recalling Legend Revo Arc Remote Reservoir FLH kits because rear suspension fluid reservoir mounting brackets may crack and break.
Product
SUSPENSION recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V264000·2024-05-06
Autocar Recalls 2020-2024 Legend Vehicles Due to Wiring Fire Risk
Autocar is recalling 2020-2024 Legend vehicles because the wiring harness may route fusible links too closely to other components, increasing the risk of a fire during a short circuit.
Product
AUTOCAR — AUTOCAR LEGEND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E036000·2024-05-06
Hiniker Recalls Snowplows Due to Electrical Overheating and Lighting Failure
Hiniker is recalling specific snowplow models because a motherboard may overheat, causing controls or lights to fail. This defect increases the risk of a crash due to reduced visibility.
Product
ELECTRICAL SYSTEM recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V317000·2024-05-06
Coach and Equipment Recalls 2024 Phoenix Shuttle Buses for Seat Defect
Coach and Equipment is recalling 2024 Phoenix shuttle buses because the seat recliner mechanism may not engage, increasing injury risk during a crash.
Product
COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V316000·2024-05-06
2024 Mercedes-Benz eSprinter Brake Control Software Defect Recall
Daimler Vans USA is recalling certain 2024 Mercedes-Benz eSprinter vehicles due to a software error in the electronic stability program that may extend braking distance and increase crash risk. Dealers will provide a free software update.
Product
MERCEDES-BENZ — MERCEDES-BENZ ESPRINTER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24E035000·2024-05-03
Autoliv Recalls Roof Rail Air Bag Inflators Due to Rupture Risk
Autoliv is recalling specific roof rail air bag inflators that may fail at the weld joint, potentially causing gas leaks or ruptures that increase injury risk.
Product
AIR BAGS:SIDE/WINDOW recall
Category
Vehicle
Distribution
Distributed nationwide