State

Vermont product recalls

73,570 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.

What the numbers show

Total: 2,011
Critical: 209
Severe: 531
Most recent: 2026-10-21

Of the 2,011 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 531 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,011 recalls whose distribution notice names Vermont specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25226–25250 of 75581

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-1796-2021·2021-06-16
Diagnostic MR imaging system hoisting blocks mechanical defect
Philips is recalling 156 Ingenia Ambition S diagnostic MR systems due to a mechanical issue detected in the lifting blocks on the magnet used during equipment movement and decommissioning.
Product
Ingenia Ambition S - Model Number: 781359 Diagnostic MR system.
Category
Medical Device
Distribution
11 states
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-1795-2021·2021-06-16
Ingenia Ambition X MRI Systems: Mechanical Defect in Hoisting Blocks
Philips has recalled 156 Ingenia Ambition X MRI systems due to a mechanical defect in the hoisting blocks used to move the magnet during decommissioning or relocation. The defect poses a risk that the magnet could fall.
Product
Ingenia Ambition X - Model Number: 781356, Diagnostic MR system. ***Updated November 2023*** Added Model Number 782109 - Ingenia Ambition X
Category
Medical Device
Distribution
11 states
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
HighFDA (Devices)·Z-1823-2021·2021-06-16
Anterior cervical plate system screw mechanism may disassociate or unlock
The Alphatec Insignia anterior cervical plate system may have a defect where the screw blocking mechanism disassociates during surgery or unlocks afterward. Consult your doctor if you have this implant.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0364 Insignia, ACP, 3-Level, 64 mm, Rx Only, Non-Sterile, UDI: (01)00190376268637
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1811-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate System screw locking mechanism failure
Alphatec Spine is recalling the Insignia Anterior Cervical Plate System due to a potential failure in the screw locking mechanism. The mechanism may disassociate or unlock during or after spinal surgery.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0240 Insignia, ACP, 2-Level, 40 mm, Rx Only, Non-Sterile, UDI: (01)00190376268408
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1817-2021·2021-06-16
Atec Insignia Anterior Cervical Plate System Screw Blocking Mechanism Risk
The FDA is recalling certain Atec Insignia Anterior Cervical Plate Systems 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 136-0352 Insignia, ACP, 3-Level, 52 mm, Rx Only, Non-Sterile, UDI: (01)00190376268576
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1821-2021·2021-06-16
Anterior Cervical Plate System Screw Blocking Mechanism May Disassociate
Alphatec Spine is recalling the Atec Insignia Anterior Cervical Plate System due to a potential defect in the screw blocking mechanism. The screws may disassociate or unlock during or after surgery, risking implant failure.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0360 Insignia, ACP, 3-Level, 60 mm, Rx Only, Non-Sterile, UDI: (01)00190376268613
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1806-2021·2021-06-16
Anterior Cervical Plate System Screw Lock Mechanism May Fail Intraoperatively or Postoperatively
The Alphatec Insignia Anterior Cervical Plate System is recalled because the screw blocking mechanism may disassociate intraoperatively or unlock postoperatively. Eight units were distributed across 15 U.S. states.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0124, Insignia, ACP, 1-Level, 24 mm, Rx Only, Non-Sterile, UDI: (01)00190376268743
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1799-2021·2021-06-16
Alphatec Insignia Anterior Cervical Plate System screw failure recalled
Alphatec is recalling its Insignia Anterior Cervical Plate System due to potential screw blocking mechanism failure during or after spinal surgery. The screw may disassociate intraoperatively or unlock postoperatively.
Product
Atec Insignia Anterior Cervical Plate System, REF 136-0116, Insignia, ACP, 1-Level, 16 mm, Rx Only, Non-Sterile, UDI: (01)00190376268422
Category
Medical Device
Distribution
Distributed nationwide