State
73,576 recalls have nationwide distribution and so reach Florida. 12,867 additional recalls listed Florida specifically in their distribution scope.
Of the 12,867 recalls naming Florida we have scored against our rubric, 1,775 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,456 (27%) are Severe.
Which agencies issued them
These figures cover only the 12,867 recalls whose distribution notice names Florida specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Percussionaire Corporation is recalling Impulsator and Phasitron 5 devices to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Tandem Diabetes Care is recalling a beta version of its t:slim iOS app because it fails to pair with Abbott FreeStyle Libre 3 Plus sensors, forcing users into manual mode.
Siemens Healthcare Diagnostics is recalling Atellica CH Revised C-Reactive Protein reagent due to the potential for falsely elevated test results.
American Nitrile Operations is recalling Performance Pro blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
Alere San Diego is recalling multiple hCG urine pregnancy test models because they may detect low hCG levels, resulting in false positive results.
NOXBOX LTD is recalling 1,667 NOxBOXi Nitric Oxide Delivery Systems due to a manufacturing issue that may cause irregular oxygen readings.
Percussionaire Corporation is recalling 98,434 In-Line Valves to update labeling warnings regarding the use of intrapulmonary percussive ventilation with volatile anesthetic delivery systems.
Heraeus Medical is recalling PALACOS MV+G pro 40 and 80 bone cement due to potential monomer liquid leakage. The recall affects 20,523 units distributed worldwide.
Wright Medical Technology is recalling 34 Charlotte Claw Screws because missing threads on the screwheads may prevent secure engagement with the plate, potentially prolonging surgery.
American Nitrile Operations LLC is recalling 36.8 million Opportunity Flex blue nitrile gloves due to defects like tears and debris that may expose users to pathogens or chemicals.
Cardinal Health 200, LLC is recalling 2,957 gynecological laparoscopy kits because the handpieces may leak fluid, creating a slip and fall hazard.
Cardinal Health 200, LLC is recalling 22 Presource Packs containing Stryker StrykeFlow PS and AHTO tube sets because the handpieces may leak fluid, creating a slip and fall hazard.
American Contract Systems Inc. is recalling medical convenience kits containing BD CliniClean Pericare Wipes due to potential lubricant contamination.
Shanghai United Imaging Healthcare is recalling 11 uCT ATLAS CT systems due to a software issue that may hide patient images, potentially requiring rescans.
ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life, while the correct validated shelf life is 5 years.
TerSera Therapeutics is recalling 296 cartons of Zoladex (goserelin) implants because the product sat in a non-temperature-controlled trailer for 25.5 hours.
ASP Global is recalling 6,100 units of 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 MPR Single Use 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 240 units of 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 MPR Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is only 5 years.
ASP Global, LLC. is recalling 1,899 units of Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the validated shelf life is 5 years.
ASP Global, LLC. is recalling 70 units of 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, but the validated shelf life is only 5 years.
Shanghai United Imaging Healthcare is recalling six uMI Panvivo S PET/CT systems due to a software defect that may hide patient images, potentially requiring rescans.
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.