State

US Virgin Islands product recalls

73,503 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: 39
Most recent: 2026-10-14

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 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24551–24575 of 73680

SevereFDA (Devices)·Z-1787-2021·2021-06-16
Dialysis access kits recalled for potential fungal contamination risk
Avid Medical is recalling medical dialysis access kits due to potential fungal growth in an applicator component that may compromise the package seal and contaminate other components. Approximately 560 kits distributed nationwide are affected.
Product
DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1539-2021·2021-06-16
COVID-19 Self-Test Kit Distributed Without Clinical Investigation Authorization
Innova Medical Group recalled COVID-19 self-test kits distributed to customers outside of clinical investigation requirements. About 1,206 tests in 402 boxes were distributed across the U.S., Canada, India, and the United Kingdom.
Product
COVID-19 Self-Test Kit *** INNOVA *** 3T
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1832-2021·2021-06-16
DeRoyal Pacemaker Tray Mislabeled With Wrong Anesthetic Concentration
DeRoyal is recalling surgical procedure packs due to mislabeling. The product contains 0.5% Bupivacaine but is labeled as 1% Lidocaine, creating a medication identification error.
Product
DeRoyal Pacemaker Tray Pgybk, REF 89-6360.06
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1537-2021·2021-06-16
FDA Recalls Innova COVID-19 Self-Test Kits Due to Unauthorized Distribution
Innova Medical Group is recalling COVID-19 self-test kits distributed to customers outside an authorized clinical investigation. The recall affects 370 boxes of tests distributed nationwide and internationally.
Product
COVID-19 Self-Test Kit *** INNOVA *** 7T
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1784-2021·2021-06-16
Adult Chest Tube Tray Recalled Due to Package Integrity Risk
Avid Medical is recalling 130 Adult Chest Tube Trays due to potential contamination from mold growth in a component. The BD ChloraPrep applicator may grow Aspergillus penicillioides, which could breach package integrity and contaminate other kit components.
Product
ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1805-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate Screw Mechanism Failure Recall
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System because the screw blocking mechanism may disassociate during surgery or unlock afterward. Eight units were distributed across 15 states.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0122, Insignia, ACP, 1-Level, 22 mm, Rx Only, Non-Sterile, UDI: (01)00190376268484
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1831-2021·2021-06-16
Laboratory Software Device May Produce Erroneous Results from Inadequate Instructions
Normand Remisol Advance Data Manager versions 1.5–1.9 have insufficient instructions for proper rule programming and testing. User-written rules may not be properly validated, potentially leading to erroneous laboratory results.
Product
Normand Remisol Advance Data Manager is a software device that interfaces between laboratory information systems (LIS) and laboratory instruments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1802-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate Screw Blocking Mechanism Disassociation Recall
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw blocking mechanism that may disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0119, Insignia, ACP, 1-Level, 19 mm, Rx Only, Non-Sterile, UDI: (01)00190376268453
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1812-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism May Fail Intraoperatively
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0242 Insignia, ACP, 2-Level, 42 mm, Rx Only, Non-Sterile, UDI: (01)00190376268415
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1844-2021·2021-06-16
Quanta System Sterile Optical Laser Fiber Recall for Potential Sterility Compromise
Quanta System is recalling 307 reusable sterile optical laser fibers nationwide due to potential sterility compromise. The affected devices were distributed through six U.S. distributors.
Product
Quanta System Sterile Optical Laser Fiber, reusable
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·21151·2021-06-16
Cove Appliance 24-inch Built-in Dishwashers Recalled for Fire Hazard
Cove Appliance is recalling about 42,000 built-in dishwashers because the heating element can fail to shut off and overheat, creating a fire hazard. The company has received five reports of burning smells, flames, and smoking inside the dishwashers, though no injuries have been reported.
Product
Cove Appliance 24-inch built-in dishwashers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1804-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Recall: Potential Screw Mechanism Failure
Alphatec Spine is recalling 7 units of the Atec Insignia Anterior Cervical Plate System because the screw blocking mechanism could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0121, Insignia, ACP, 1-Level, 21 mm, Rx Only, Non-Sterile, UDI: (01)00190376268477
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1813-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System recall due to potential screw mechanism failure
Alphatec Spine is recalling Atec Insignia Anterior Cervical Plate System units due to a potential defect where the screw blocking mechanism may disassociate or unlock during or after surgery. No adverse events have been reported.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0244 Insignia, ACP, 2-Level, 44 mm, Rx Only, Non-Sterile, UDI: (01)00190376268507
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1838-2021·2021-06-16
Medical Device Software Defects in RayStation Treatment Planning System
RayStation radiation therapy treatment planning software versions 6 through 10A contain defects that may cause misleading dose evaluations and contouring errors. Healthcare facilities should verify treatment plans and contact the manufacturer for guidance.
Product
RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24 , 6.1.1.2 , 6.2.0.7 , 6.3.0.6 , 7.0.0.19 , 8.0.0.6 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 , 9.2.0.483 , 10.0.0.1154 , 10.0.1.52 or 10.1.0.613 .
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1820-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Screw Mechanism Recall
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to potential disassociation or postoperative unlock of the screw blocking mechanism during or after cervical spine surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0358 Insignia, ACP, 3-Level, 58 mm, Rx Only, Non-Sterile, UDI: (01)00190376268606
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1801-2021·2021-06-16
Anterior cervical plate system screw mechanism may disassociate during or after surgery
Alphatec Spine's Atec Insignia Anterior Cervical Plate System has a potential defect where the screw blocking mechanism may disassociate during or after surgery, which could compromise spinal stabilization.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0118, Insignia, ACP, 1-Level, 18 mm, Rx Only, Non-Sterile, UDI: (01)00190376268446
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1803-2021·2021-06-16
Cervical Spine Plate System Screw Mechanism May Disassociate or Unlock
Alphatec Spine recalls its Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism, which may disassociate or unlock during or after spinal surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0120, Insignia, ACP, 1-Level, 20 mm, Rx Only, Non-Sterile, UDI: (01)00190376268460
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1824-2021·2021-06-16
Alphatec Insignia Cervical Plate System: Screw Mechanism Disassociation Risk
Alphatec recalls the Insignia Anterior Cervical Plate System due to risk that the screw blocking mechanism may disassociate during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0468 Insignia, ACP, 4-Level, 68 mm, Rx Only, Non-Sterile, UDI: (01)00190376268675
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1822-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism Recall
Alphatec Spine recalls Atec Insignia Anterior Cervical Plate Systems because the screw blocking mechanism may fail during or after surgery. The mechanism may disassociate or unlock, potentially compromising implant stability.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0362 Insignia, ACP, 3-Level, 62 mm, Rx Only, Non-Sterile, UDI: (01)00190376268620
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1842-2021·2021-06-16
FDA Recalls Olympus Sterile Optical Laser Fibers for Potential Sterility Compromise
Quanta System is recalling Olympus Sterile Optical Laser Fibers nationwide due to potentially compromised sterility. Approximately 26,925 units distributed through six U.S. distributors are affected.
Product
Olympus Sterile Optical Laser Fiber, single use and reusable
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1815-2021·2021-06-16
Anterior Cervical Plate System Recalled for Potential Screw Mechanism Failure
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System because the screw blocking mechanism could disassociate or unlock during or after cervical spine surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0250 Insignia, ACP, 2-Level, 50 mm, Rx Only, Non-Sterile, UDI: (01)00190376268538
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1846-2021·2021-06-16
Radiotherapy positioning software may delay patient movement display
Brainlab's ExacTrac Dynamic radiotherapy positioning software may delay display of patient movement during high-dose treatments, risking treatment precision errors. 22 systems affected across 11 U.S. states.
Product
ExacTrac Dynamic software, Model 20910-01B ETD Positioning and Monitoring Installer 1.0.2 - Product Usage: intended to position patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures, to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1814-2021·2021-06-16
Anterior Cervical Plate System Screw Mechanism May Disassociate or Unlock
Alphatec Spine recalls its Insignia Anterior Cervical Plate System because the screw blocking mechanism may disassociate during spinal surgery or unlock afterward. Healthcare providers should contact the manufacturer for guidance.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0248 Insignia, ACP, 2-Level, 48 mm, Rx Only, Non-Sterile, UDI: (01)00190376268521
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1827-2021·2021-06-16
Anterior cervical plate system screw blocking mechanism defect recalled
Alphatec Spine's Atec Insignia anterior cervical plate system has a defect in the screw blocking mechanism that could disassociate or unlock during or after surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0482 Insignia, ACP, 4-Level, 82 mm, Rx Only, Non-Sterile, UDI: (01)00190376268712
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1809-2021·2021-06-16
Anterior cervical plate system screw blocking mechanism may disassociate
Alphatec Spine Inc. is recalling the Atec Insignia anterior cervical plate system because the screw blocking mechanism may disassociate intraoperatively or unlock postoperatively. No injuries reported.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0236 Insignia, ACP, 2-Level, 36 mm, Rx Only, Non-Sterile, UDI: (01)00190376268385
Category
Medical Device
Distribution
Distributed nationwide