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.

9876–9900 of 73269

ModerateFDA (Devices)·Z-2874-2024·2024-09-04
Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes
Beaver Visitec International is voluntarily recalling 216 units of BVI CustomEyes Procedure Packs containing low dead space and luer slip tip syringes manufactured by Sol-M. The recall affects nationwide distribution.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001484;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2787-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling 19 units of BVI CustomEyes Procedure Packs because they contain Sol-M syringes subject to a separate voluntary recall.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584630;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2859-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-Millennium Medical syringes (Part Number 58001331, Lot 6069181). The voluntary recall affects approximately 357 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001331;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2902-2024·2024-09-04
BVI CustomEyes Procedure Packs Containing Sol-M Syringes Recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing low dead space and luer slip tip syringes manufactured by Sol-Millennium Medical. The voluntary recall affects 29 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001695;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2854-2024·2024-09-04
BVI CustomEyes Procedure Packs with Defective Syringes Recalled Nationwide
BVI CustomEyes Procedure Packs containing Sol-M syringes are being voluntarily recalled due to a defect in the syringes.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001304;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2847-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes due to a voluntary recall by the syringe manufacturer. The recall affects 43 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001138;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2789-2024·2024-09-04
BVI CustomEyes Procedure Packs containing syringes recalled nationwide
BVI CustomEyes Procedure Packs containing Sol-M syringes are subject to a voluntary recall affecting 73 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584712;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2852-2024·2024-09-04
Medical Device Syringe Recall: BVI CustomEyes Procedure Packs
BVI CustomEyes Procedure Packs containing Sol-M syringes are subject to a voluntary recall. The recall affects 148 units distributed in the US.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001200;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2939-2024·2024-09-04
Beaver Visitec CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec International is recalling CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip syringes due to a voluntary recall by the syringe manufacturer, Sol-Millennium Medical, Inc.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002080;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2824-2024·2024-09-04
BVI CustomEyes Procedure Packs Containing Sol-M Syringes Recalled
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes. The recall affects 489 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000781;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2719-2024·2024-09-04
Cobra EMG ET Tube Recalled Due to Incorrect Size Labeling
Neurovision Medical Products recalls Cobra 3-Plate EMG ET Tubes due to mislabeling with incorrect tube size on the label. The error could affect proper product selection in clinical procedures.
Product
Cobra, 3-Plate EMG ET Tube, 6.0mm, REF: LTE7003PM, not made with natural rubber latex, Rx Only, STERILEEO
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2853-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes. Approximately 77 units were distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001212;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2887-2024·2024-09-04
BVI CustomEyes Procedure Packs Recalled for Defective Syringes
BVI is voluntarily recalling CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. A total of 97 units have been distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001602;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2856-2024·2024-09-04
BVI CustomEyes Procedure Packs With Sol-M Syringes Voluntarily Recalled
Beaver Visitec International voluntarily recalls BVI CustomEyes Procedure Packs (Part Number 58001306, Lot 6072093) containing Sol-M manufactured syringes. The recall affects 206 units distributed nationwide due to a voluntary recall by the syringe manufacturer.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001306;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2880-2024·2024-09-04
BVI CustomEyes Procedure Packs With Sol-M Syringes Recalled Voluntarily
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs that contain syringes manufactured by Sol-Millennium Medical due to a voluntary recall by the syringe manufacturer.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001526;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2782-2024·2024-09-04
BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The voluntary recall affects 247 units distributed nationwide.
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584404;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·24V649000·2024-09-03
2025 Mazda CX-50 Forward Sensing Camera Malfunction Disables Safety Systems
Mazda is recalling 2025 CX-50 and certain 2024 models due to a forward sensing camera malfunction that may prevent automatic emergency braking and lane-keep assist systems from functioning, increasing crash risk.
Product
MAZDA — MAZDA MAZDA3, CX-30, CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24V648000·2024-09-03
2023 Nova Bus LFS Buses Recalled for Defective Instrument Panel Firmware
Nova Bus is recalling certain 2023-2024 LFS buses due to defective instrument panel firmware that may fail to display the speedometer or warning lights, and may cause loss of drive power, increasing crash risk.
Product
NOVA BUS — NOVA BUS LFS ARTIC, LFS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·24V646000·2024-08-30
E-One Recalls Cyclone and Typhoon Vehicles Due to Crossmember Defect
E-One is recalling 2022-2024 Cyclone and Typhoon vehicles because a broken engine crossmember can damage the cooling fan, potentially causing an engine stall and increasing crash risk.
Product
E-ONE — E-ONE CYCLONE II, CYCLONE N, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·24E074000·2024-08-30
Alltrade Recalls Kilimanjaro E-bike Racks Due to Connection Point Cracking
Alltrade Tools LLC is recalling Kilimanjaro E-bike racks sold at Costco because connection points may crack, causing the rack to fail and the bicycle to detach.
Product
EQUIPMENT:MECHANICAL:CARRIER/RACK recall
Category
Consumer Product
Distribution
Distributed nationwide
CriticalCPSC·24350·2024-08-29
HALO 1000 Portable Power Stations Recalled for Fire and Burn Hazards
About 5,740 HALO 1000 Portable Power Stations are recalled because their lithium-ion batteries can overheat and catch fire. One death from smoke inhalation and four fire incidents have been reported.
Product
HALO 1000 Portable Power Stations
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24352·2024-08-29
Glow in Dark Party Supplies Toy Sets Recalled for Battery Ingestion Hazard
Glow in Dark Party Supplies Toy Sets sold on Amazon contain button cell batteries in Bunny Ears Headbands that can be easily accessed by children, posing a serious ingestion hazard. The sets violate federal battery-operated toy regulations.
Product
Glow in Dark Party Supplies Toy Sets
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·24351·2024-08-29
Fisher-Price Dumbbell Toy Recalled for Choking Hazard
Fisher-Price is recalling a plastic dumbbell toy sold in the Baby Biceps Gift Set because the gray caps on the ends can come off, posing a choking hazard to infants. The firm has received seven reports of the ends coming off but no injuries have been reported.
Product
Dumbbell toy sold with Baby Biceps Gift Set
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·24V644000·2024-08-29
Altec Recalls 2024 Spray Trucks and Aerial Devices for Line Security Defect
Altec is recalling 623 units of 2024 spray trucks and aerial devices because fuel or brake lines may not be properly secured, posing risks of brake failure or fire.
Product
ALTEC — ALTEC SPRAY TRUCK, TA CLASS, AT SERIES
Category
Vehicle
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2636-2024·2024-08-28
McGrath Mac Video Laryngoscope battery depletion may cause thermal event and explosion
McGrath Mac Video Laryngoscope devices may experience battery management system failures causing batteries to deplete below design thresholds, potentially resulting in thermal events and explosions.
Product
McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
Category
Medical Device
Distribution
Distributed nationwide