State

US Virgin Islands product recalls

73,584 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

Of the 178 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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27826–27850 of 73762

ModerateFDA (Devices)·Z-2848-2020·2020-09-02
Siemens Cios Alpha and Spin Mobile X-Ray Systems Recalled for Electrical Malfunction
Siemens is recalling Cios Alpha and Cios Spin mobile X-ray systems because a hardware error could cause permanent loss of imaging functionality.
Product
Cios Alpha (VA20) - Model: 10308191 Cios Alpha (VA30) - Model: 11105200 Cios Spin (VA30) - Model: 10308194 Cios Alpha and Cios Spin are a mobile X-Ray system designed to provide X-ray imaging of the anatomical structures of patient during clinical applications
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2900-2020·2020-09-02
Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Defect
Neurovision is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Product
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 6.0mm REF NVTKIT-C6-5, Rx Only, Sterile, UDI: B006NVTKITC652/$$7061918A - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2901-2020·2020-09-02
Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Defect
Neurovision Medical Products Inc. is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially stopping EMG signal transmission and rendering the device unusable.
Product
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMT ET Tube, 7.0mm REF: NVTKIT-C7-5, RxOnly, Sterile, UDI: B006NvtKITc752/$$7062818C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2898-2020·2020-09-02
Siemens E.cam and Symbia Systems Recalled for Detector Time Loss
Siemens Medical Solutions is recalling E.cam and Symbia systems with foresight detectors because they may lose detector time information during gated or dynamic acquisitions.
Product
E.cam or Symbia systems that use foresight detectors - Product Usage: To detect or image the distribution of radionuclides in the body or organ, using the following techniques: planar imaging, whole body imaging, tomographic imaging for isotopes with energies up to 588keV.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2904-2020·2020-09-02
Neurovision Cobra EMG ET Tube Recalled for Insulating Material Softening
Neurovision Medical Products Inc. is recalling Cobra x5 1-Ch EMG ET Tubes because the electrode insulating material may soften, potentially damaging the device and stopping signal transmission.
Product
Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5, Rx Only, Sterile EO CE UDI: B006LTE700M52/$$7061418C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2899-2020·2020-09-02
RayCare Oncology Software Recalled for Offline Image Review Error
RaySearch Laboratories AB is recalling RayCare oncology software due to an error message that may prevent users from accessing offline images during review tasks.
Product
RayCare, device is stand-alone software - Product Usage: used to support workflows and scheduling, as well as clinical information, planning and treatment management for oncology care.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1539-2020·2020-09-02
Ecolab Recalls Hand Sanitizer Due to Discoloration and Foreign Substance
Ecolab Inc is recalling 305 drums of 55-gallon hand sanitizer nationwide due to discoloration and the presence of a foreign substance.
Product
Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab Inc 1 EcoLab Place St. Paul, MN 55102 USA, NDC 47593-624-21
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1533-2020·2020-09-02
Hikma Recalls Buprenorphine Hydrochloride Injection Due to Low Potency
Hikma Pharmaceuticals is recalling 97,890 vials of Buprenorphine Hydrochloride Injection because stability testing revealed the drug was sub-potent.
Product
BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2905-2020·2020-09-02
Neurovision Cobra EMG Endotracheal Tubes Recalled for Insulation Softening
Neurovision is recalling Cobra x5 1-Ch EMG ET Tubes because the electrode insulating material may soften over time, potentially damaging the device and stopping EMG signal transmission.
Product
Cobra x5 1-Ch EMG ET Tube, 8.0mm, REF: LTE700L-5, Rx Only, Sterile EO UDI: B006LTE700L52$$7061318B - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2875-2020·2020-09-02
Ortho-Clinical Diagnostics Recalls VITROS XT Chemistry TBIL-ALKP Slides
Ortho-Clinical Diagnostics is recalling VITROS XT Chemistry TBIL-ALKP Slides due to potential interference from etrombopag that may affect total bilirubin test results.
Product
VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected) In Vitro Diagnostic use only - The TBIL test within the VITROS XT Chemistry Products TBIL-ALKP Slides quantitatively measures total bilirubin (TBIL) concentration in serum and plasma, Product Code: 6844296
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2874-2020·2020-09-02
Ortho-Clinical VITROS Chemistry BuBc Slides Recalled for Etrombopag Interference
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products BuBc Slides because the drug etrombopag interferes with the test results.
Product
VITROS Chemistry Products BuBc Slides - in vitro diagnostic use only. VITROS Chemistry Products BuBc Slides quantitatively measure unconjugated bilirubin (Bu) and conjugated bilirubin (Bc) concentrations in serum and plasma, Product code: 8383051 (60 slide); 1612365 (18 slide)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2902-2020·2020-09-02
Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Softening
Neurovision is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially damaging the device and stopping EMG signal transmission.
Product
Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 mm, REF NVTKIT-C8-5, Rx Only, Sterile UDIB006NVTKITC852/$$7062118C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1541-2020·2020-09-02
Red Cross Oral Pain Relief Recalled for Cotton Pellet Labeling Error
The Mentholatum Company is recalling Red Cross Oral Pain Relief blister packs because the included cotton pellet box incorrectly lists Natural Eugenol Oil as an ingredient.
Product
RED CROSS ORAL PAIN RELIEF — RED CROSS ORAL PAIN RELIEF (BENZOCAINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2886-2020·2020-09-02
Match Point System surgical instrument recalled due to incorrect procedure side labeling
The Match Point System surgical instrument was recalled because the procedure side on planning reports was incorrectly marked as 'Left' instead of 'Right' for right-side procedures.
Product
Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2877-2020·2020-09-02
OraSure Benzodiazepine Micro-Plate Recalled for Incorrect Lot Number Labeling
OraSure Technologies is recalling 13 kits of Interept Benzodiazepine Micro-Plates due to incorrect lot numbers on specification sheets and unit boxes.
Product
Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD Immunoassay for Benzodiazepines, Product Number: 1110IT
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-2876-2020·2020-09-02
OraSure Benzodiazepine Micro-Plate Recall Due to Incorrect Lot Number Labeling
OraSure Technologies is recalling 39 kits of the Interept Benzodiazepine Micro-Plate EIA due to incorrect lot numbers on the specification sheet and unit box.
Product
Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepines, Product Number: 1110IB
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V529000·2020-09-01
Daimler Trucks Recalls Freightliner Chassis Due to Tire Valve Stem Risk
Daimler Trucks is recalling certain Freightliner chassis because a tire valve stem extension may contact the wheel rim, potentially causing a loss of tire pressure and increasing crash risk.
Product
FCCC — FCCC XCM, XCR, MC, XCL
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V528000·2020-09-01
2020-2021 BMW X5, X6, X7 Headlamp Non-Compliance Recall
BMW is recalling certain 2020-2021 X5, X6, and X7 models because their headlamps may emit unintended blue light, which could confuse oncoming drivers and increase crash risk. Dealers will replace affected headlamps at no cost.
Product
BMW — BMW X6, X5, X7
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E062000·2020-09-01
Harbor Freight Recalls Pittsburgh Automotive A/C Manifold Gauge Sets
Harbor Freight is recalling Pittsburgh Automotive A/C Manifold Gauge Sets due to swapped labels that may cause pressurized refrigerant release and injury.
Product
EQUIPMENT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·20V527000·2020-09-01
Engine harness defect may cause stalling in 2018–2021 Freightliner trucks
Engine harness wires may chafe and short in certain 2018–2021 Freightliner trucks, causing unexpected engine stalling that can increase crash risk.
Product
FREIGHTLINER — FREIGHTLINER 114SD, 108SD, BUSINESS CLASS M2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V525000·2020-08-31
Fontaine Recalls 2016-2020 Freightliner 114SD Autohaulers for Battery Cable Fire Risk
Fontaine is recalling 1,074 2016-2020 Freightliner 114SD Autohaulers because cab movement may damage the battery cable, creating a fire risk.
Product
FREIGHTLINER — FREIGHTLINER 114SD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V526000·2020-08-31
MCI Recalls 2017-2020 J4500 Motor Coaches for Coolant Hose Failure
Motor Coach Industries is recalling 2017-2020 J4500 motor coaches because a coolant hose may fail, causing engine shutdown and coolant spills that increase crash risk.
Product
MCI — MCI J4500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V521000·2020-08-28
Heartland Bighorn Traveler landing legs may collapse causing trailer to drop
Certain 2019-2021 Heartland Cyclone, 2020-2021 Bighorn Traveler, and 2020-2021 Elkridge recreational trailers may have insufficient bracing on the front landing legs, which could buckle and collapse while parked, causing the trailer to drop unexpectedly.
Product
HEARTLAND — HEARTLAND CYCLONE, ELKRIDGE, BIGHORN TRAVELER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V522000·2020-08-28
PJ Trailers DE Trailer Hydraulic Cylinder Bolts May Fail
PJ Trailers is recalling 2020-2021 DE model trailers. The attachment bolts securing the hydraulic cylinder may fail when the dump box is operated, creating a risk that the box could suddenly drop and injure a person.
Product
PJ TRAILERS — PJ TRAILERS DE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V523000·2020-08-28
Grand Design Solitude recreational trailers recalled for propane gas leak risk
Grand Design Solitude recreational trailers (2017-2021) are being recalled because the propane supply line may contact the refrigerator burner tube, potentially causing a propane gas leak and increasing fire risk.
Product
GRAND DESIGN — GRAND DESIGN SOLITUDE
Category
Vehicle
Distribution
Distributed nationwide