State

US Virgin Islands product recalls

72,913 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 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1801–1825 of 73090

HighFDA (Food)·H-0770-2026·2026-05-20
Dakota Honey salted caramel spun honey may contain foreign objects
Dakota Honey Company Spreadable Spun Honey in salted caramel flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Product
Dakota Honey Company Spreadable Spun Honey, Salted Caramel. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41981 4. 2. Net Wt 12 oz (340g) UPC 8 60010-57964 0.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·H-0771-2026·2026-05-20
Dakota Honey jalapeno spun honey may contain metal or plastic pieces
Dakota Honey Company Spreadable Spun Honey in jalapeno flavour is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Product
Dakota Honey Company Spreadable Spun Honey, Jalapeno. Stir before use. Produced in Winner, SD. Packaged in the following sized plastic jars: 1. Net Wt 4 oz (113g) UPC 8 60012-41982 1. 2. Net Wt 12 oz (340g) UPC 8 60010-57965 7.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2184-2026·2026-05-20
Reprocessed electrophysiology catheters recalled over incomplete sterile seals
The CS Uni-Directional with Auto ID reprocessed electrophysiology catheter is being recalled because of incomplete seals on the sterile product. 449 units are affected.
Product
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2197-2026·2026-05-20
Daig Livewire Steerable Reprocessed Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling 458 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.
Product
Daig Livewire Steerable, Product Number 401932; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2163-2026·2026-05-20
Dexcom G7 CGM iOS App Software Defect Delays Glucose Alerts
Dexcom, Inc. is recalling versions 2.9.0 through 2.11.2 of the Dexcom G7 Continuous Glucose Monitoring iOS app due to a software defect that delays glucose value notifications and alerts, risking missed detection of dangerous blood sugar events.
Product
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number: SW12300 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM iOS App Component: Dexcom G7 Continuous Glucose Monitoring System,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2194-2026·2026-05-20
Daig Livewire Steerable Reprocessed Electrophysiology Catheters Recalled
Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product packaging. The defect may compromise sterility.
Product
Daig Livewire Steerable, Product Number 401914; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2165-2026·2026-05-20
Dexcom ONE+ iOS CGM App Software Defect Delayed Glucose Alerts
Dexcom, Inc. is recalling Dexcom ONE+ iOS CGM App versions 1.5.0 and 1.6.0 due to a software defect that can delay glucose alerts and notifications, risking delayed detection of low or high blood sugar events.
Product
Brand Name: Dexcom ONE+ Continuous Glucose Monitoring System Product Name: Dexcom ONE+ iOS CGM App Model/Catalog Number: SW14244 Software Version: versions 1.5.0 and 1.6.0 Product Description: Dexcom ONE+ iOS CGM App Component: Dexcom ONE+ Continuous Glucose Monitoring Syste
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2187-2026·2026-05-20
Reprocessed Electrophysiology Catheter Recall Due to Incomplete Sterile Seals
Stryker Sustainability Solutions is recalling 108 units of Daig Livewire Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging. The defect may compromise sterility assurance.
Product
Daig Livewire Steerable, Product Number 401581; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0772-2026·2026-05-20
Dakota Honey Flight four-flavour gift packs may contain foreign objects
The Dakota Honey Company Honey Flight, a four-flavour spun honey set, is being recalled because of a foreign object: stainless steel dust or flakes, or shreds of plastic.
Product
Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original - Salted Caramel - Cinnamon - Jalapeno. UPC 8 60010-57968 8. 4 - 4 oz (340g) jars. Net Wt 16 oz (454g). Produced in Winner, SD.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2181-2026·2026-05-20
Reprocessed Electrophysiology Catheter Recalled for Incomplete Sterile Seals
Stryker Sustainability Solutions is recalling 217 units of BARD EP XT Decapolar Steerable reprocessed electrophysiology catheters due to incomplete seals on the sterile product packaging.
Product
BARD EP XT Decapolar Steerable, Product Number 201007; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2191-2026·2026-05-20
Daig Livewire Steerable Electrophysiology Catheter Incomplete Seals Recall
Stryker Sustainability Solutions is recalling Daig Livewire Steerable reprocessed electrophysiology catheters (Product Number 401904) due to incomplete seals on sterile product. The recall affects 1,352 units distributed across the United States, Israel, and Canada.
Product
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2169-2026·2026-05-20
QuickVue Dipstick Strep A Test Recalled for False Positive Results
Quidel Corporation is recalling the QuickVue Dipstick Strep A Test (50T, REF 20108) due to the potential for false positive results. The product was distributed nationwide.
Product
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2182-2026·2026-05-20
BARD EP XT Steerable Reprocessed Electrophysiology Catheter Recall
Stryker Sustainability Solutions is recalling BARD EP XT Steerable reprocessed electrophysiology catheters due to incomplete seals on sterile product, which may compromise sterility. Affected units were distributed in the US, Israel, and Canada.
Product
BARD EP XT Steerable, Product Number 200794; REPROCESSED ELECTROPHYSIOLOGY CATHETER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2164-2026·2026-05-20
Dexcom G7 app defect may delay glucose readings and alerts
Dexcom G7 CGM iOS and watchOS app versions 2.9.0 through 2.11.2 are being corrected because a software defect can delay glucose value and alert processing.
Product
Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM watchOS App Model/Catalog Number: SW13355 Software Version: Versions 2.9.0 through 2.11.2 Product Description: Dexcom G7 CGM watchOS App - The watchOS app is installed along with the iOS ph
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2166-2026·2026-05-20
Thermedx FluidSmart Urology Tube Set recalled for nonconforming products
Stryker Corporation is recalling the Thermedx FluidSmart Urology Tube Set (Catalog No. LL0006) due to nonconforming products that were inadvertently distributed. The affected tube sets were distributed nationwide in Georgia.
Product
Thermedx FluidSmart Urology Tube Set REF LL0006 UDI-DI code: 00860936000365 The FluidSmart Tube Sets are intended to be used with the FluidSmart Fluid Management System, which is intended for irrigation and fluid warming in laparoscopic procedures, and distention, fluid warmi
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2155-2026·2026-05-20
Revolution Apex Select CT systems subject to software security vulnerability recall
GE HealthCare is recalling Revolution Apex Select and related CT systems due to a security vulnerability in the AW Server software deployed via Edison Health Link-based CT Smart Subscription.
Product
Revolution Apex Select, X-ray Computed Tomography, Model Number 5590000-27
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2172-2026·2026-05-20
Edwards EVOQUE Tricuspid Delivery System Labeling Update for Valve Functionality
Edwards Lifesciences is updating labeling for the Edwards EVOQUE tricuspid delivery system (REF 9850TDS) to provide a warning if valve replacement delivery system functionality becomes compromised.
Product
Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2152-2026·2026-05-20
Revolution Apex Plus CT System Security Vulnerability Recall
GE HealthCare is recalling Revolution Apex Plus X-ray CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link. Eleven units are affected worldwide.
Product
Revolution Apex Plus, X-ray Computed Tomography, Model Number 5590000-25
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2173-2026·2026-05-20
Codman CerebroFlo EVD Catheter recalled for out-of-specification endotoxin
Integra LifeSciences is recalling Codman CerebroFlo EVD Catheters (Lot 45322) because endotoxin levels did not meet acceptance criteria. The product was distributed nationwide.
Product
Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD Catheter is a 3.3 mm diameter (10 Fr.), 35 cm long polyurethane catheter for diverting cerebrospinal fluid (CSF) from the ventricles of the brain through a series
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0547-2026·2026-05-20
Metoprolol Succinate Extended-Release Tablets Recalled Due to Failed Dissolution
Ascend Laboratories is recalling 17,304 bottles of Metoprolol Succinate Extended-Release 25 mg tablets (Lot #25140859, expiring Jan 2027) distributed nationwide because the tablets failed dissolution specifications, which may affect drug effectiveness.
Product
METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE ER TABLETS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2154-2026·2026-05-20
Revolution Apex X-ray CT System Security Vulnerability Recall
GE HealthCare is recalling Revolution Apex, Revolution Ascend, and Revolution CT systems due to a potential security vulnerability in the AW Server deployed via Edison Health Link-based CT Smart Subscription. The vulnerability may impact system security.
Product
Revolution Apex, X-ray Computed Tomography, Model Number 5590000-20
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2171-2026·2026-05-20
ZYMUTEST HIA IgG ELISA Diagnostic Kit Recall for Incorrect Control Values
Aniara Diagnostica LLC is recalling ZYMUTEST HIA IgG diagnostic kits (Lot FD1265) due to an outdated flyer containing incorrect positive control values that could affect test result interpretation.
Product
ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref. RK040A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2134-2026·2026-05-20
DonJoy IceMan Classic Cube cold therapy unit connector defect recall
DJO, LLC is recalling DONJOY ICEMAN CLASSIC CUBE cold therapy units due to broken connectors that may interrupt prescribed cold therapy. Approximately 596 units were distributed nationwide and in Canada.
Product
Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product Description: 11-0494 - ICEMAN CLASSIC CUBE The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMan¿ helps pro
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2137-2026·2026-05-20
DonJoy IceMan cold therapy unit recall due to broken connector
DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit (model 11-9099) due to a broken connector that may interrupt prescribed cold therapy. The affected unit is lot 110525, distributed across the US and Canada.
Product
Brand Name: DONJOY Product Name: ICEMAN, W/COLDPAD, NS, RH Model/Catalog Number: 11-9099 Software Version: No Product Description: 11-9099 - ICEMAN, W/COLDPAD, NS, RH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMa
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2136-2026·2026-05-20
DonJoy IceMan CLASSIC3 Cold Therapy Unit Connector Fault Recall
DJO, LLC is recalling the DonJoy IceMan CLASSIC3 cold therapy unit (Model 11-1424) due to a broken connector that may interrupt prescribed cold therapy treatment.
Product
Brand Name: DONJOY Product Name: ICEMAN W/,UNIV,LOOP,NS,EH Model/Catalog Number: 11-1424 Software Version: No Product Description: 11-1424 - ICEMAN W/,UNIV,LOOP,NS,EH The IceMan CLASSIC3¿ cold therapy unit helps reduce pain and swelling, speeding up rehabilitation. The IceMa
Category
Medical Device
Distribution
Distributed nationwide