State

US Virgin Islands product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4276–4300 of 73117

CriticalFDA (Devices)·Z-0444-2026·2025-11-19
Open heart and vascular kits recalled over cracked anesthesia circuit tubing
Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Product
Anesthesia Circuit Kits and other various kits that contain Anesthesia Circuits; OPEN HEART SUPPLEMENT DYNJ909116D; VASCULAR DYNJ909124F
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0186-2026·2025-11-19
Green Maeng Da kratom powder recalled over potential Salmonella contamination
Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Product
Monarch Premium Kratom Green Maeng Da powder is packaged in seal mylar pouches: Monarch Premium Kratom Green Maeng Da, 4oz powder (112g), UPC 851006008466 Monarch Premium Kratom Green Maeng Da, 0.5oz powder (14g), UPC 851006008770 Monarch Premium Kratom Green Maeng Da, 2
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·H-0187-2026·2025-11-19
Red Bali kratom powder recalled over potential Salmonella contamination
Lotus Vaping Technologies is recalling Monarch Premium Kratom Red Bali powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Product
Monarch Premium Kratom Red Bali powder is packaged in seal mylar pouches: Monarch Premium Kratom Red Bali, 4oz powder (112g), UPC 851006008442 Monarch Premium Kratom Red Bali, 8oz powder (224g), UPC 706970483859 Monarch Premium Kratom Red Bali, 2oz powder (56g), UPC 8510060084
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V799000·2025-11-19
2026 Tiffin Open Trail Motorhomes Recalled Due to Incorrect Cargo Capacity Labels
Tiffin Motorhomes, Inc. is recalling certain 2026 Open Trail motorhomes because the cargo carrying capacity labels may be incorrect, which could lead to vehicle overloading.
Product
TIFFIN — TIFFIN OPEN TRAIL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0183-2026·2025-11-19
Tense-X supplement recalled because it contains magnesium salicylate
Professional Botanicals is recalling 253 bottles of Tense-X capsules because the product contains magnesium salicylate.
Product
Product Name: Tense-X. Package: 175cc HDPE Bottle. Type: Vegetable Capsule. Count: 60. Dose: 2 Capsules. Product Sku: PB207
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0498-2026·2025-11-19
Long nasal feeding tubes recalled from one lot for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 90 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0454-2026·2025-11-19
CARESCAPE ONE monitors recalled over batteries that fail to hold charge
GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
CARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2026·2025-11-19
VATS lobectomy stapler boxes recalled over a malformed cover tube press
Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0182-2026·2025-11-19
Dietary supplement recalled because it contains magnesium salicylate
Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.
Product
Product Name: Total Comfort. Package: 175cc HDPE Bottle. Type: Vegetable Capsule Count: 60, Dose: 2 Capsules. Product Sku: PB173.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0477-2026·2025-11-19
Maryland jaw sealers 44 cm recalled over trapped residual material
Medline is recalling 9,547 reprocessed LigaSure Maryland Jaw sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Maryland Jaw Sealer/Divider NanoCoated, Compatible with FT10 Generator 44 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2026·2025-11-19
Impact vessel sealers recalled over residual material that may dislodge
Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0471-2026·2025-11-19
Five millimetre blunt tip sealers recalled over trapped residual material
Medline is recalling two reprocessed LigaSure Blunt Tip sealer/dividers, 5 mm x 37 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Blunt Tip Sealer/Divider, Compatible with FT10 Generator, 5 mm x 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0455-2026·2025-11-19
Bedside patient monitors recalled over batteries that fail as backup power
GE Healthcare is recalling 7,408 B105P, B125P, B105M, B125M and B155M patient monitors because certain batteries can lose the ability to hold charge, causing a loss of monitoring.
Product
B105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2026·2025-11-19
Oxygen concentrator batteries recalled over a chip that can stop oxygen
Philips Respironics is recalling 56 SimplyGo Mini standard battery kits because a defective chip can make the battery fail, shutting down the concentrator and stopping oxygen delivery.
Product
SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2026·2025-11-19
Blunt tip sealers 44 cm recalled over trapped residual material
Medline is recalling 1,446 reprocessed LigaSure Blunt Tip sealer/dividers, 44 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 44cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0467-2026·2025-11-19
LigaSure Exact dissectors recalled over residual material that may dislodge
Medline is recalling 4,226 reprocessed LigaSure Exact dissectors, 21 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Exact, Dissector without Nano-Coating 21cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical Cutting And Coagulation Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0482-2026·2025-11-19
Electrosurgical snares recalled over small holes compromising package sterility
Olympus is recalling 48,208 Single Use Electrosurgical Snares SD-400 because sterility may be compromised by small holes formed during packaging or transportation.
Product
Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and/or cauterization of di
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0453-2026·2025-11-19
Patient monitors recalled over batteries that can lose backup power
GE Healthcare is recalling 3,271 Carescape B450 patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
Carescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE M
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0483-2026·2025-11-19
Fifteen millimetre snares recalled over holes compromising package sterility
Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.
Product
Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instruments have been designed to be used with an Olympus endoscope for the removal and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0470-2026·2025-11-19
Small jaw sealers recalled over residual material that may dislodge
Medline is recalling 18,117 reprocessed LigaSure Small Jaw instruments because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Small Jaw Instrument (Purple/White), Compatible with FT10 Generator 18.8 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0485-2026·2025-11-19
Surgical staplers recalled over a malformed cover tube press
Covidien is recalling 3,263 Signia Small Diameter Curved Tip Intelligent Reloads because a manufacturing issue can allow internal components to move during firing, risking uncontrolled motion.
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); CFN: SIGSDL45CTVT;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0472-2026·2025-11-19
Short blunt tip sealers recalled over residual material that may dislodge
Medline is recalling 65 reprocessed LigaSure Blunt Tip sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline RenewalLigasure Blunt Tip Sealer/Divider, NanoCoated Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0473-2026·2025-11-19
Blunt tip sealers recalled over residual material trapped inside the device
Medline is recalling 60,917 reprocessed LigaSure Blunt Tip sealer/dividers, 37 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal Ligasure Blunt Tip Sealer/Divider NanoCoated, Compatible with FT10 Generator 37 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0497-2026·2025-11-19
Larger bore nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 6 F-8 F x 55 nasal feeding tubes with stylet and ENfit from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2026·2025-11-19
Maryland jaw sealers 23 cm recalled over residual material inside the device
Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide