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.

4301–4325 of 73117

HighFDA (Devices)·Z-0452-2026·2025-11-19
Lithotripsy transducers recalled over startup failures and handpiece temperature rise
Olympus is recalling 1,528 ShockPulse Lithotripsy Transducers because the device may fail to start or stop shortly after starting, and the handpiece body may heat up during clinical use.
Product
Brand Name: Lithotriptor, Ultrasonic Product Name: ShockPulse Lithotripsy Transducer Model/Catalog Number: SPL-T Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse tra
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0493-2026·2025-11-19
Food allergen panels recalled over barcodes causing wrong tube scanning order
Siemens Healthcare Diagnostics is recalling 28 units of Food Panel 3 Specific Allergen because barcode orientation causes the instrument to misread tube positions in the holder wedge.
Product
Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;
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-0476-2026·2025-11-19
Reprocessed vessel sealers recalled over residual material that may dislodge
Medline is recalling 57,244 reprocessed LigaSure Maryland Jaw sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider NanoCoated, Compatible w/FT10 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-0494-2026·2025-11-19
Nasal feeding tubes recalled from a second lot for possible occlusion
Applied Medical Technology is recalling NutraGlide 5 F-6 F x 55 nasal feeding tubes with stylet and ENfit, REF NFT-05055-I, from one lot because the tube may be occluded.
Product
Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
Category
Medical Device
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 (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-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-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-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-0496-2026·2025-11-19
Ninety centimetre nasal feeding tubes recalled for possible occlusion
Applied Medical Technology is recalling NutraGlide 5 F-6 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, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0495-2026·2025-11-19
Nasal feeding tubes recalled from one lot because they may be occluded
Applied Medical Technology is recalling NutraGlide 5 F-6 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, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2026·2025-11-19
Allergy IgE universal kits recalled over barcodes misordering tubes in wedges
Siemens Healthcare Diagnostics is recalling 2,802 units of the 3gAllergy Specific IgE Universal Kit because barcode orientation causes the instrument to misread tube positions.
Product
3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; Catalog Number: L2KUN6;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0480-2026·2025-11-19
Mobile X-ray systems recalled over bolts that may loosen or fracture
NeuroLogica is recalling 236 GM85 digital mobile X-ray systems because the four M5 bolts securing the tube head unit to the arm may loosen or fracture from metal fatigue.
Product
GM85 Digital Mobile X-ray imaging System; Model Number: GM85;
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V800000·2025-11-19
McNeilus Recalls 2024-2025 Volterra ZSL Trucks Due to Software Error
McNeilus is recalling 2024-2025 Volterra ZSL side loader garbage trucks because a software error may cause grabber fingers to move without operator input, posing a risk of injury or crash.
Product
MCNEILUS — MCNEILUS VOLTERRA ZSL
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0478-2026·2025-11-19
Spinal fixation screws recalled for not meeting performance standards
Orthofix is recalling 624 Virata preassembled polyaxial screws used in the Virata Spinal Fixation System because the screws do not meet performance standards.
Product
Virata Preassembled Polyaxial Screw, utilized in the Virata Spinal Fixation System. The following sizes are affected: 1. POLYAXIAL SCREW, CC, 5.5mm X 30mm; Item Number: TL1-10755030. 2. POLYAXIAL SCREW, CC, 5.5mm X 35mm; Item Number: TL1-10755035. 3. POLYAXIAL SCREW, CC
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-0456-2026·2025-11-19
Portrait vital signs monitors recalled over batteries losing backup power
GE Healthcare is recalling 5,990 Portrait VSM patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0479-2026·2025-11-19
ACL restoration implants recalled from one lot held in sales stock
Miach Orthopaedics is recalling 167 BEAR Implants from a single lot, in an action the record says was limited to sales force trunk stock.
Product
BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0461-2026·2025-11-19
ProxiDiagnost systems recalled over ceiling carriages that resist vertical movement
Philips is recalling 41 ProxiDiagnost N90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
ProxiDiagnost N90; Model Number: 706110;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0465-2026·2025-11-19
DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement
Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0464-2026·2025-11-19
DigitalDiagnost 4 systems recalled over ceiling carriages hard to move
Philips is recalling 12 DigitalDiagnost 4 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0466-2026·2025-11-19
Radiography systems recalled over ceiling carriages that are hard to move
Philips is recalling 284 Radiography 7300 C systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
Radiography 7300 C; Model Number: 712037;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0462-2026·2025-11-19
CombiDiagnost systems recalled over ceiling carriages that resist vertical movement
Philips is recalling 17 CombiDiagnost R90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
CombiDiagnost R90; Model Number: 709031;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0484-2026·2025-11-19
Laboratory cuvette arrays recalled over barcodes the analyser cannot read
Becton Dickinson is recalling 29,760 BD Kiestra Isolate Suspension Cuvette Arrays because formatting errors in the 2D barcodes stop the analyser reading the expiration date.
Product
BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
Category
Medical Device
Distribution
Distributed nationwide