State
73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline is recalling 3,125 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
W L Gore & Associates is recalling 32 units of GORE VIABIL Short Wire Biliary Endoprosthesis because they may be mislabeled with the incorrect length.
Medline is recalling 620 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements, which may cause leaking or breaking during use.
Boston Scientific is recalling 403 units of NaviFlex LW Pusher and Advx Panc. Stent devices due to an incorrect manufacturing feature.
Cook Incorporated is recalling 97 Williams Cystoscopic Injection Needles because a component may not be correctly seated, potentially causing inadequate treatment.
Medline is recalling 235 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Integrated Medcraft is recalling FORWARD Gunshot Wound Kits because the sterile pad may degrade, potentially causing material to dislodge on or near wounds.
BioFire Diagnostics is recalling specific lots of FilmArray Pneumonia Panel Plus kits due to potential contamination that could cause false positive results.
Microgenics Corporation is recalling MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control products due to vial-to-vial variability that may delay patient PTH results.
BioFire Diagnostics is recalling specific lots of FilmArray Pneumonia Panels due to potential contamination that could result in false positive test results.
Houston Rx LLC is recalling 7 vials of Sermorelin injectable solution due to a lack of process control. The product was distributed nationwide.
Medline is recalling 30 Foot Ankle convenience kits due to a discrepancy in the shelf-life of a component.
BioFire Diagnostics is recalling specific lots of the Joint Infection Panel due to potential contamination that could cause false positive test results.
Neuronetics is recalling 179 NeuroStar Advanced Therapy Systems because the cables in the HP Coil Assembly do not meet product specifications.
Healthmark Industries is recalling 12.8 million vinyl instrument guards because their labeling does not comply with FDA regulations and steam sterilization instructions have been updated.
Medline is recalling 165 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.
Medline Industries is recalling 3,551 CONMED AirSeal Access Port kits due to potential overpressure alerts and system venting that may delay or end procedures.
In2bones USA, LLC is recalling 29 bone screws labeled as fully threaded but actually partially threaded due to a labeling error.
Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports because they may produce erroneous overpressure alerts and system venting.
Radiometer Medical ApS is recalling ABL90 FLEX and ABL90 FLEX PLUS analyzers due to a risk of potentially inaccurate results requiring updated instructions for use.
Merit Medical Systems is recalling Scout MD Delivery Systems because the implantable clip may fail to deploy, preventing the reflector from functioning as intended.
Magellan Diagnostics is recalling 321 LeadCare II Blood Lead Test Kits due to a potential expiration date labeling error that may delay test results.
Toyota is recalling 2022-2024 Lexus NX vehicles because the instrument panel may fail to display critical warnings, increasing crash risk.
Hyundai is recalling 2026 Tucson Hybrid and Elantra vehicles because improperly tightened front strut fasteners may cause a loss of steering control.
Ford is recalling 2026-2027 Lincoln Nautilus and 2027 Corsair Hybrids because corrosion may cause the vehicle to unexpectedly shift into neutral while driving.