State

US Virgin Islands product recalls

72,969 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 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6276–6300 of 73146

HighFDA (Devices)·Z-1888-2025·2025-06-11
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack recalled
Mozarc Medical is recalling Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack units due to a potential breach of sterile barrier packaging. The affected catheter models were distributed nationwide in the US and in Canada and Mexico.
Product
Palindrome Precision H Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1896-2025·2025-06-11
Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Product
Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1897-2025·2025-06-11
Signature Laparoscopic Bullet Tip Grasper Instrument Insulation Defect Recall
Silex Medical is recalling 6 units of the Signature Laparoscopic Bullet Tip Grasper with Rotating Shaft due to incomplete insulation on the shaft near the rotator wheel, which could expose users to electrical hazards.
Product
Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863030.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V365000·2025-06-11
Mercedes-Benz Recalls 2023 GLC 300 Models for Missing Headlight Caps
Mercedes-Benz is recalling 2023 GLC 300 and GLC 300 4MATIC vehicles because missing caps allow improper headlight adjustment, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLC 300, GLC 300 4MATIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V368000·2025-06-11
Nova Bus turn signal indicator lights may remain solidly illuminated
Nova Bus is recalling certain 2022-2023 LFS buses because a digital display firmware error may leave the instrument panel turn signal indicators solidly lit, failing FMVSS 108.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1909-2025·2025-06-11
Pre-filled Water Syringe recalled for improper use contamination
Healthmark Industries is recalling Pre-filled Water Syringes (Model SW-010-100 and SW-010) after duodenoscope contamination was linked to improper use of the syringes outside their intended purpose.
Product
Pre-filled Water Syringe, Model Numbers SW-010-100 and SW-010
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1891-2025·2025-06-11
FoundationOne Companion Diagnostic F1CDx Incorrect Claim Display
Foundation Medicine is recalling the FoundationOne Companion Diagnostic (F1CDx) due to an incorrect negative claim displayed on the claims page, though device variant information was correctly shown in the tumor profiling section of the approved test report.
Product
FoundationOne Companion Diagnostic (F1CDx)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0457-2025·2025-06-11
Lacosamide Oral Solution recalled for defective leaking containers
Apotex Corp. is recalling Lacosamide Oral Solution because certain bottles may leak when stored horizontally. Patients taking this seizure medication should contact their pharmacy or healthcare provider.
Product
Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0458-2025·2025-06-11
Hand Sanitizer Recalled for Subpotent Ethyl Alcohol Content
Spectrum Advanced Gel Hand Sanitizer (70% ethyl alcohol, 8 FL OZ) has been recalled nationwide because affected batches contain cloudy appearance and test below the claimed 70% alcohol concentration, making them less effective.
Product
HAND SANITIZER — HAND SANITIZER (ETHYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0454-2025·2025-06-11
Indomethacin Extended-Release Capsules recalled for cGMP deviations
Amerisource Health Services LLC is recalling Indomethacin Extended-Release Capsules 75 mg due to cGMP (current Good Manufacturing Practice) deviations. The recall affects 21 cartons distributed nationwide.
Product
INDOMETHACIN — INDOMETHACIN (INDOMETHACIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2025·2025-06-11
Beckman Coulter Sample Probe Manufacturing Defect Recall
Beckman Coulter Mishima is recalling sample probes due to a manufacturing defect where rounded and chamfered corners prevent proper air layer formation, causing sample dilution and inaccurate test results.
Product
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1913-2025·2025-06-11
DxI 9000 Access Immunoassay Analyzer Software Update Error Codes
Beckman Coulter is recalling DxI 9000 Access Immunoassay Analyzers running software version 1.20 because the update introduces error codes that prevent assays from being performed and may delay result generation.
Product
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1890-2025·2025-06-11
FoundationOne Companion Diagnostic contains incorrect negative claims
Foundation Medicine is recalling two FoundationOne Companion Diagnostic (F1CDx) test reports that contained an incorrect negative claim on the claims page, though the device variant information displayed correctly in the tumor profiling section.
Product
FoundationOne Companion Diagnostic (F1CDx)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V331000·2025-06-10
Hyundai Translead Recalls 2026 Dry Van Trailers for Liftgate Pin Defect
Hyundai Translead is recalling 2026 Dry Van Trailers because insufficient lubrication on the liftgate cylinder pin may cause it to seize, leading to liftgate failure and injury risk.
Product
HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DRY VAN TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V382000·2025-06-10
Mack Trucks Recalls 2025 Anthem and Granite Models for Electrical Short Risk
Mack Trucks is recalling 2025 Anthem and Granite vehicles because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.
Product
MACK — MACK GRANITE (GR), ANTHEM (AN)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V364000·2025-06-10
Forest River trailer side gate latches may unlock during transit
Forest River is recalling certain 2025 Salem and Wildwood travel trailers because the side entry gate latch may unlock, allowing the strut to open the gate during transit.
Product
FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V350000·2025-06-09
Ford Recalls 2025 Maverick Vehicles Due to Loose Air Bag Indicator Light
Ford is recalling 2025 Maverick vehicles because the air bag indicator light may be loose or dislodged, potentially failing to warn occupants of a deactivated air bag.
Product
FORD — FORD MAVERICK
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V381000·2025-06-09
Braun Recalls 1,533 Vehicles for Loose Seat Belt Fasteners
Braun is recalling 1,533 Chrysler Pacifica, Voyager, and Toyota Sienna vehicles because seat belt tie-down fasteners may be loose, increasing injury risk in crashes.
Product
BRAUN — BRAUN CHRYSLER PACIFICA, CHRYSLER VOYAGER, TOYOTA SIENNA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V332000·2025-06-06
Volvo Recalls 2025-2026 VN Trucks for Power Cable Routing Defect
Volvo Trucks North America is recalling 2025-2026 Volvo VN trucks because improperly routed power cables may cause electrical shorts, leading to engine stalls or fires.
Product
VOLVO — VOLVO VN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V375000·2025-06-06
2018–2024 Harley-Davidson Softail motorcycles rear shock issue
Harley-Davidson is recalling certain 2018–2024 Softail motorcycles because the rear shock pre-load adjuster mounting tab may break and damage the tire, causing sudden loss of pressure and increasing crash risk.
Product
HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FLHCS ANV, FXLRS, FXLRST
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V379000·2025-06-06
Mercedes-Benz GLC 300 and AMG GLC models roof impact protection
Mercedes-Benz is recalling certain 2023–2025 GLC 300 and GLC 300 4MATIC, 2024–2025 AMG GLC 43 4MATIC, 2025 GLC 350E 4MATIC, and 2025 AMG GLC 63 S E vehicles with panoramic sunroofs. The C-pillar may not absorb adequate impact in a crash, increasing injury risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E 4MATIC, GLC 300 4MATIC, AMG GLC63 S E, GLC 300
Category
Vehicle
Distribution
Distributed nationwide
CriticalCPSC·25316·2025-06-05
Portable Hook-On Chairs Recalled for Fall Hazard and Serious Injury Risk
Portable hook-on chairs sold on Amazon by Ravmix pose a fall hazard because the crotch restraint can be removed without tools, allowing infants to fall through. The product violates federal safety standards. Consumers should stop using immediately and contact Ravmix for refund instructions.
Product
Portable Hook-On Chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25311·2025-06-05
BowFlex Adjustable Dumbbells Recalled Due to Dislodging Weight Plates
About 3.8 million BowFlex 552 and 1090 adjustable dumbbells are recalled because weight plates can dislodge from the handle during use. Over 100 injuries have been reported, including concussions and broken toes.
Product
BowFlex 552, 52.5 LB Adjustable Dumbbells and BowFlex 1090, 90 LB Adjustable Dumbbells
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·25V378000·2025-06-05
Honda CR-V Hybrid fuel feed hose may be improperly installed
Honda is recalling certain 2025 CR-V Hybrid vehicles because the fuel feed hose may have been improperly installed, allowing fuel to leak. This fails FMVSS 301.
Product
HONDA — HONDA CR-V HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·25322·2025-06-05
Apollo America Combination Smoke and Carbon Monoxide Detectors Recalled
Apollo America 51000-600 combination smoke and carbon monoxide detectors can malfunction and fail to alert users to fire or CO leaks, risking smoke inhalation, CO poisoning, or death. Vivint is sending free replacement detectors to all known purchasers.
Product
Apollo America 51000-600 Combination Smoke and Carbon Monoxide Detectors
Category
Consumer Product
Distribution
Distributed nationwide