Recalls affecting Vermont
Notices that name Vermont in their distribution area, plus every nationwide recall — nationwide recalls reach Vermont too.
-
Class III · 1+ years ago
Hi-Tech Pharmaceuticals Inc. Hi-Tech Pharmaceuticals Beta Sitosterol Provides Support recall: Unapproved Drug Claims and Misbranded
Unapproved Drug Claims and Misbranded.
-
Class III · 1+ years ago
Hi-Tech Pharmaceuticals Inc. Primenutrition Taurine Mental & Athletic Performance 125 recall: Unapproved Drug Claims and Misbranded
Unapproved Drug Claims and Misbranded.
-
NHTSA safety recall · 1+ years ago
Porsche Cars recall: The fasteners securing the high pressure fuel pump may not be tightened
The fasteners securing the high pressure fuel pump may not be tightened properly, resulting in a fuel leak.
-
NHTSA safety recall · 1+ years ago
Volvo Trucks New VN recall: The door latch cable on the interior door handle may be incorrectly
The door latch cable on the interior door handle may be incorrectly installed, preventing the door from opening.
-
NHTSA safety recall · 1+ years ago
Volvo Trucks New VN recall: When towing a trailer, the trailer lights may fail to illuminate
When towing a trailer, the trailer lights may fail to illuminate due to an improperly manufactured body control module.
-
Highest risk · 1+ years ago
Wuensche USA Ambiano Cotton Candy Makers recall: Fire Hazard; Sold at ALDI
Fire Hazard; Sold at ALDI
-
Highest risk · 1+ years ago
Five Below Tabletop Fire Pits recall: Risk of Serious Burn Injury from Flame Jetting and Fire Hazards
Risk of Serious Burn Injury from Flame Jetting and Fire Hazards
-
Highest risk · 1+ years ago
Arizer Solo II portable electronic vaporizer devices recall: The internal lithium-ion battery can overheat, produce smoke
The internal lithium-ion battery can overheat, produce smoke, and/or eject material, posing fire and burn hazards.
-
NHTSA safety recall · 1+ years ago
BMW recall: The torsion bar in both front seat belt retractors may have been damaged
The torsion bar in both front seat belt retractors may have been damaged during production.
-
Class II · 1+ years ago
Siemens Healthcare Diagnostics, Inc. Atellica CH Urinary/Cerebrospinal Fluid Protein recall: Potential for falsely depressed patient, quality control (QC)
Potential for falsely depressed patient, quality control (QC), and/or calibration results or delayed results.
-
Class II · 1+ years ago
B.Braun Medical S.A.S. Brand Name: Celsite Product Name: Celsite Babyport SET PUR 4 recall: The potential for minor injury such as damage to the vessel and/or tearing
The potential for minor injury such as damage to the vessel and/or tearing of the vessel wall.
-
Class II · 1+ years ago
Contract Medical International GmbH Brand Name: Fortress Introducer Sheath System recall: Units may have been packaged with an incorrect pouch label
Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the…
-
Class II · 1+ years ago
NOxBOXi Nitric Oxide Delivery System recall: Replacement of the internal Sample Pump due to high failure rates
Replacement of the internal Sample Pump due to high failure rates.
-
Class II · 1+ years ago
Omnia Medical TiBrid Stand Alone Intervertebral Body Fusion Device recall: Failure of fusion system instruments in the field
Failure of fusion system instruments in the field.
-
Class II · 1+ years ago
AVID Medical, Inc. Halyard, CPT Basic IR Pack recall: Potential for open header bag seals, compromising sterility
Potential for open header bag seals, compromising sterility.
-
Class II · 1+ years ago
Waldemar Link GmbH & Co. KG LinkSymphoKnee System, Tibial Component recall: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured
Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.
-
Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: Altivate Reverse Wedge recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
-
Class II · 1+ years ago
Merit Medical Systems, Inc. 10Fore Hemostasis Valve recall: Due to a manufacturing issue involving the silicone quad ring where the ring
Due to a manufacturing issue involving the silicone quad ring where the ring is deformed or otherwise damaged and may cause a foreign body in the…
-
Class II · 1+ years ago
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical recall: Retroactive; Due to complaints, labeling correction for permanent
Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would…
-
Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: Altivate Reverse Wedge recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
-
Class II · 1+ years ago
Omnia Medical TiBrid Stand Alone Intervertebral Body Fusion Device recall: Failure of fusion system instruments in the field
Failure of fusion system instruments in the field.
-
Class II · 1+ years ago
Boston Scientific Corporation Preventive Maintenance Kit Icefx recall: Certain desiccant tube subassemblies were built with end caps
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
-
Class II · 1+ years ago
Encore Medical, LP Brand Name: DJO Surgical Product Name: FA S Altivate Reverse recall: Their is a potential that the reamer may kick or bind up during
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
-
Class II · 1+ years ago
Seaspine Orthopedics Corporation Reef TA Inserter recall: Inserter, used as part of a system with an intervertebral body fusion device
Inserter, used as part of a system with an intervertebral body fusion device, may contribute to difficulty disengaging the implant or improper…