State

US Virgin Islands product recalls

72,966 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: 2026-09-09

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 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5776–5800 of 73143

HighFDA (Devices)·Z-2169-2025·2025-07-30
CareLink SmartSync limited the window to abort a high voltage therapy
Medtronic CareLink SmartSync Device Manager is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Product
Medtronic CareLink SmartSync Device Manager, Model Number 24967A with the following software components: 1. Cobalt Crome application, Software Model Number D00U005; 2. Claria Amplia Compia application, Software Model Number D00U009; 3. Evera MRI application, Software Mod
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2130-2025·2025-07-30
SIGNA Architect gradient coils can produce acoustic noise above the limit
GE HealthCare SIGNA Architect MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Product
SIGNA Architect
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2025·2025-07-30
SIGNA PET/MR gradient coils can produce acoustic noise above the limit
GE HealthCare SIGNA PET/MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Product
SIGNA PET/MR
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2165-2025·2025-07-30
Biofinity XR Toric contact lens blisters may have a leaking seal
Biofinity XR Toric Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 397 units are affected.
Product
Biofinity XR Toric Contact Lens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2166-2025·2025-07-30
Biofinity Toric Multifocal contact lens blisters may have a leaking seal
Biofinity Toric Multifocal Contact Lenses are being recalled because lens blisters may have an incomplete or leaking seal, which may render them unsterile. 827 units are affected.
Product
Biofinity Toric Multifocal Contact Lens
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2025·2025-07-30
Nellcor bedside SpO2 monitor alarms may not be heard or recognized
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
Product
Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N, 10005941-SG, DS10005941, 10005941J, 10005941JP, 10005941JPN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2135-2025·2025-07-30
HSG procedure trays label non-sterile iodine pouches as sterile
HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.
Product
HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and sonohysterography procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2132-2025·2025-07-30
Discovery MR750w gradient coils can produce acoustic noise above the limit
GE HealthCare Discovery MR750w 3.0T MR systems are being recalled because gradient coils can produce acoustic levels exceeding the 99 dB limit set by IEC 60601-2-33 during scanning.
Product
Discovery MR750w 3.0T
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0537-2025·2025-07-30
Clomipramine capsules failed a degradation product specification at expiry testing
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
Product
CLOMIPRAMINE HYDROCHLORIDE — CLOMIPRAMINE HYDROCHLORIDE (CLOMIPRAMINE HYDROCHLORIDE CAPSULES)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2163-2025·2025-07-30
ACUVUE OASYS MAX multifocal daily lenses have bubbles and voids
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Product
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0536-2025·2025-07-30
Compounded quadruple ophthalmic solution returned subpotent assay results in stability testing
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
Product
Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25E046000·2025-07-29
Terran Industries Recalls 7000lb Axle Assemblies Due to Suspension Defect
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Product
SUSPENSION:MULTIPLE AXLE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V495000·2025-07-29
Mack Recalls 2026 Granite Trucks Due to Brake Drum Incompatibility
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Product
MACK — MACK GRANITE GR (4)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V493000·2025-07-28
Kia K5 rear window trim pieces may loosen and detach
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V494000·2025-07-28
Kia Telluride door belt molding trim can delaminate and detach
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Product
KIA — KIA TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V492000·2025-07-28
Porsche Recalls 2024-2025 Macan 4 Electric for Air Bag Defect
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Product
PORSCHE — PORSCHE MACAN 4 ELECTRIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V491000·2025-07-28
Grech motorhome awnings can extend unintentionally during transit
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Product
GRECH — GRECH STRADA, TURISMO, TERRENO
Category
Vehicle
Distribution
Distributed nationwide
ModerateNHTSA·25V490000·2025-07-28
2026 Tesla Model Y vehicles recalled for inoperable horn
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
Product
TESLA — TESLA MODEL Y
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-07272025-01·2025-07-27
USDA Alerts on Ham Salad Products with Recalled Breadcrumbs
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Product
Reser's Fine Foods, Inc. — FSIS Issues Public Health Alert For Ready-To-Eat Ham Salad Products Containing FDA-Regulated Breadcrumbs That Have Been Recalled Due to Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V488000·2025-07-25
Ford electronic brake booster can fail losing power brake assist
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.
Product
FORD — FORD, LINCOLN F-150, EXPEDITION, BRONCO, RANGER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V487000·2025-07-25
Mercedes EQB battery bus bar screws can cause sudden power loss
Mercedes-Benz is recalling certain 2022-2023 EQB 300 and EQB 350 4MATIC vehicles because the high voltage battery bus bar may be secured with incorrect screws, causing a sudden loss of drive power.
Product
MERCEDES-BENZ — MERCEDES-BENZ EQB 300 4MATIC, EQB 350 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V486000·2025-07-25
Forest River Recalls 2025-2026 Motorhomes Due to Fuel Line Fire Risk
Forest River is recalling 2025-2026 Sunseeker, Solera, and other motorhomes because fuel line connectors may detach, creating a fire hazard.
Product
FOREST RIVER — FOREST RIVER, EAST TO WEST SUNSEEKER, SOLERA, LEPRECHAUN, FREELANDER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V489000·2025-07-25
Ford Recalls 2025 F-150 Hybrid for Seat Belt Warning Chime Defect
Ford is recalling 2025 F-150 Hybrid vehicles because the seat belt warning chime may not activate. Dealers will update software to fix the issue.
Product
FORD — FORD F-150 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25E047000·2025-07-25
Ford Recalls Bronco Upfit Kits Due to Rearview Camera Compatibility Issues
Ford is recalling specific Bronco Upfit kits because the rearview camera may not display an image, increasing crash risk. Dealers will replace the camera free of charge.
Product
BACK OVER PREVENTION: SENSING SYSTEM: CAMERA recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V480000·2025-07-25
BMW motorcycle emergency call system may have been deactivated
BMW is recalling certain 2025 motorcycles with the optional emergency call system because a software programming error may have deactivated eCall, so first responders may not be notified of a crash.
Product
BMW — BMW R 1300 GS ADVENTURE, R 1300 GS, F 800 GS, F 900 GS
Category
Vehicle
Distribution
Distributed nationwide