State
72,971 recalls have nationwide distribution and so reach Florida. 12,821 additional recalls listed Florida specifically in their distribution scope.
Of the 12,821 recalls naming Florida we have scored against our rubric, 1,765 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,975 (23%) are Severe.
Which agencies issued them
These figures cover only the 12,821 recalls whose distribution notice names Florida specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Braun Industries is recalling 2023-2026 ambulances because a damaged brake pedal switch may prevent cruise control from disengaging, increasing crash risk.
Autocar is recalling 2024-2026 Xpeditor and Legend vehicles because an improperly secured tie rod clamp may separate, causing loss of steering control.
Chrysler is recalling specific Mopar Gear Shift Control Cables that may detach from the transmission, preventing the vehicle from shifting into park and increasing the risk of a crash.
About 175,000 Scripto Premium Torch lighters are being recalled because they violate the mandatory safety standard for multipurpose lighters, posing fire and burn hazards.
About 920 Mom Genius retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor.
About 1,300 Bellabu Bear bamboo sherpa children's robes are being recalled because they violate the mandatory flammability standards for children's sleepwear.
Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.
About 5,800 sets of 1,000 three-millimetre magnetic balls are being recalled because the loose high-powered magnets pose an ingestion hazard to children.
About 740 Bmrwtg LED tutu skirts are being recalled because children can easily access the lithium coin batteries and the skirts lack the warnings required by Reese's Law.
About 490 YGJT baby loungers sold on SHEIN.com are being recalled because low sides, oversized foot openings and the lack of a stand create an unsafe infant sleeping environment.
Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.
Medline is recalling 88 Extremity Pack convenience kits that were labeled as sterile but never went through the sterilization process.
Medline is recalling 7,913 reprocessed ACUSON AcuNav ultrasound catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Siemens is recalling 498 MAGNETOM Vida (DE) MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Siemens is recalling one BIOGRAPH One (DE) system because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Medline is recalling 828 VALVE PACK-LF kits because they contain lots of cannula products where the catheter may not retain its shape.
Siemens is recalling 59 MAGNETOM Verio Dot systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Siemens is recalling 22 MAGNETOM Cima.X (DE) systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Siemens is recalling 56 MAGNETOM Skyra fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Draeger is recalling 530 Atlan A350 anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
A MAGNETOM Connectom.X MRI system is being recalled because an ice blockage in the magnet venting system could prevent helium from escaping during a quench.
Siemens is recalling 27 Biograph mMR systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Medline is recalling 7,913 reprocessed Livewire Steerable Electrophysiology Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.