State
73,576 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.
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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Shanghai United Imaging Healthcare is recalling three uMI Panvivo PET/CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling Ingenia 1.5T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate processing by third-party software.
ASP Global, LLC. is recalling 36 units of Expressaire Disposable BB Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling Expressaire disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling 400 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Olympus is recalling 543 DisplayPort cables used with the OLYSENSE Hub System because they may cause video dropouts or blackouts during high-power operation.
ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Percussionaire Corporation is recalling IPV-2C and Phasitron 5 devices to update labeling warnings regarding the use of these devices with volatile anesthetic delivery systems.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
FDA is recalling 34 United Imaging uMI 550 PET/CT systems due to a software issue that can hide patient images, potentially requiring rescans.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling 91 Evolution MRI systems because Enhanced MR DICOM exports contain incorrect diffusion directions, preventing correct tractography reconstruction.
Philips is recalling Ingenia 3.0T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.
ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
Philips is recalling 107 MR 7700 MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing accurate tractography reconstruction.
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm.
Apotex Corp. is recalling Paroxetine Hydrochloride Extended-Release Tablets, 37.5mg, because they failed dissolution specifications.