State

US Virgin Islands product recalls

73,092 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 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10326–10350 of 73269

HighFDA (Devices)·Z-2437-2024·2024-07-31
Perfusor Space Syringe Pump Recalled for Monoject Syringe Incompatibility Risk
B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.
Product
Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Non-Wireless Model/Catalog Number: 8713032U Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0616-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled for Subpotent Menthol Content
Hemp Bombs CBD Pain Freeze is being recalled because the menthol content is weaker than the labeled 4% claim. The recall affects 2,082 bottles distributed nationwide.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC Code: 8-40078-56612-7
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0613-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content
Hemp Bombs CBD Pain Freeze is being recalled because the menthol potency is less than the labeled 4%. Consumers should stop using the affected product and return it to the retailer.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, NDC 73423-003-01; UPC Code: 8-40078-56493-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0614-2024·2024-07-31
Nature's Script CBD Pain Relief Roll-On Recalled for Subpotent Menthol
FDA Class III recall of Nature's Script CBD Cryotherapy Pain Relief Roll-on (200mg, 1 oz bottles) due to subpotent menthol content less than the labeled 4%. The product did not contain the claimed amount of active ingredient.
Product
Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634, UPC code: 8-40078-56731-5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2439-2024·2024-07-31
Medical device diagnostic software vulnerability causes potential application crashes
Siemens Sensis Vibe diagnostic systems may crash when documentation functionality is used during certain reporting events. Seven units were distributed to facilities nationwide.
Product
Sensis Vibe systems with software version VD15B in combination with VM VIRTUAL SERVER Model: 10765502-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radi
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2425-2024·2024-07-31
Cystatin C Diagnostic Reagent Marketed Without FDA 510(k) Clearance
Randox Laboratories is recalling 115 kits of RX Series CYSC Cystatin C Reagent because it was marketed without required FDA 510(k) clearance. Healthcare facilities should discontinue use and contact the manufacturer.
Product
RX Series CYSC- Cystatin C Reagent -Intended for in vitro diagnostic (IVD) use as Randox Cystatin C assay on automated analysers. Catalogue Number: CYS4004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2422-2024·2024-07-31
MIC-KEY Gastric-Jejunal Feeding Tube Kits Recalled for Incomplete Safety Information
Avanos Medical is recalling MIC-KEY Gastric-Jejunal Feeding Tube Kits because the Instructions for Use were missing required risk information about potential complications. No illnesses have been reported.
Product
MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 0270xx (Non-ENFIT); and MIC-KEY* Gastric-Jejunal Feeding Tube Kit, Extension Sets with ENFit Connectors, Endoscopic / Radiologic Placement, Low-Profile GJ-Tube, REF 8270xx, ste
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0615-2024·2024-07-31
Hemp Bombs CBD Pain Freeze Recalled Due to Subpotent Menthol Content
Global Widget LLC is recalling Hemp Bombs CBD Pain Freeze (4% menthol) because the menthol concentration is below the labeled claim. Approximately 11,130 bottles were distributed nationwide.
Product
Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles, Distributed by: Global Widget 8419 Sunstate St, Tampa FL 33634; UPC code: 8-40078-56497-0
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0618-2024·2024-07-31
Homeopathic Kit Recalled for Label Mix-up Between Products
Washington Homeopathic Products is recalling 11 Complete 30C/200C Homeopathic Kits nationwide due to a labeling error. Some bottles labeled as Ferrum Metallicum 200C actually contain Ferrum Phosphoricum 200C.
Product
Complete 30C/200C Homeopathic Kit, Contains: One hundred 1/2 dram vials of homeopathic medicines, Washington Homeopathic Products, Inc., Berkley Springs, WV 25411, UPC 7 40640 64300 6.
Category
Drug
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2024-EXP·2024-07-30
Boar's Head Expands Recall of Deli Meats Due to Listeria
Boar's Head is recalling 7 million pounds of ready-to-eat meat and poultry products due to possible Listeria contamination linked to a multistate outbreak.
Product
Boar's Head Provisions Co., Inc. — Boar's Head Provisions Co. Expands Recall for Ready-To-Eat Meat and Poultry Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·24E063000·2024-07-30
Mevotech Recalls Aftermarket Front Lower Control Arms Due to Design Flaw
Mevotech is recalling specific aftermarket front lower control arms because a design flaw may cause the ball joint to separate, increasing crash risk.
Product
SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V567000·2024-07-30
Mack truck seat and belt anchorage bolts may be improperly tightened
Mack is recalling certain 2024-2025 Anthem, Granite and Pinnacle vehicles with RollTek driver's seats because the seat pedestal and seat belt attachment may have been improperly tightened.
Product
MACK — MACK PINNACLE (PI/PN), ANTHEM (AN), PIONEER PR (4), GRANITE (GR)
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V566000·2024-07-30
Tiffin motorhome chassis controller can blow a fuse shutting down engine
Tiffin is recalling certain 2022-2025 Phaeton, Allegro Bus and Zephyr motorhomes because the PowerGlide chassis controller may have insufficient circuit protection, which can blow a fuse and shut down the engine.
Product
TIFFIN — TIFFIN PHAETON, ZEPHYR, ALLEGRO BUS
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·023-2024·2024-07-26
Boar's Head Recalls Deli Meats Due to Listeria Contamination
Boar's Head Provisions is recalling liverwurst and other deli meats nationwide due to possible Listeria monocytogenes contamination linked to a multistate outbreak.
Product
Boar's Head Provisions Co., Inc. — Boar's Head Provisions Co. Recalls Ready-To-Eat Liverwurst And Other Deli Meat Products Due to Possible Listeria Contamination
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·24E062000·2024-07-26
Meritor Recalls Replacement Tie Rods Due to Heat-Treatment Defect
Meritor is recalling replacement tie rods with specific USK ball studs that may break due to incorrect heat treatment, risking loss of steering control.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V564000·2024-07-26
Nova Bus window glazing may reduce the driver's visibility
Nova Bus is recalling certain 2019-2023 LFS and LFS Artic buses because the glazing used on the glass windows may reduce the driver's visibility, failing FMVSS 205.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V557000·2024-07-26
BMW R 1300 GS starter motor relays may overheat
BMW is recalling certain 2024 R 1300 GS motorcycles because the starter motor relay housing may have been manufactured incorrectly, resulting in a damaged relay that can overheat.
Product
BMW — BMW R 1300 GS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V561000·2024-07-26
Hyundai Santa Fe floor wiring may chafe against the second row seat
Hyundai is recalling certain 2024 Santa Fe and Santa Fe Hybrid vehicles because the main floor wiring harness may chafe and become damaged, affecting airbag deployment.
Product
HYUNDAI — HYUNDAI SANTA FE HYBRID, SANTA FE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V563000·2024-07-26
Forest River Cherokee Travel Trailer Recall for Microwave Fire Risk
Forest River is recalling 2025 Cherokee CKT20-0G travel trailers because an incorrect screw in the microwave compartment can cause electrical arcing and fire.
Product
FOREST RIVER — FOREST RIVER CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V556000·2024-07-25
Second Navistar recall covers incorrectly heat treated tie rod ball studs
A second Navistar recall covers certain 2025 International HV, HX, LT, MV and RH vehicles whose tie rod ball studs may have been incorrectly heat-treated. 573 units affected.
Product
INTERNATIONAL — INTERNATIONAL HX, LT, RH, HV
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V562000·2024-07-25
Hyundai Recalls 2010-2013 Genesis Coupe for Ignition Spring Fracture Risk
Hyundai is recalling 2010-2013 Genesis Coupe vehicles because a fractured ignition spring may cause unintended movement when started in gear.
Product
HYUNDAI — HYUNDAI GENESIS COUPE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24321·2024-07-25
Hover-1 Dynamo E-Scooters Recalled Due to Brake Failure Risk
DGL Group is recalling about 4,200 Hover-1 Dynamo e-scooters sold on Walmart.com from November 2021 through July 2022 because the brakes can fail, creating a serious injury and crash hazard. The company has received 22 reports of brake failure resulting in seven injuries.
Product
Hover-1 Dynamo E-scooters
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24315·2024-07-25
Ophanie Large Pink Area Rugs Recalled for Fire Hazard
Ophanie large pink area rugs sold on Amazon violate federal flammability regulations and pose a fire hazard. About 5,200 units sold from April through June 2024 are being recalled.
Product
Ophanie Large Pink Area Rugs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·24V559000·2024-07-25
Nova Bus Recalls 2019-2021 LFS Models Due to Brake Chamber Defect
Nova Bus is recalling 166 LFS and LFS Artic buses because a defective brake chamber may leak air, causing unexpected braking, overheating, or fire.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V558000·2024-07-25
Nova Bus Recalls 2016-2019 LFS Models Due to Brake Chamber Defect
Nova Bus is recalling 2016-2019 LFS and LFS Artic buses because a defective brake chamber may leak air, causing unexpected braking, overheating, or fire.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide