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.
Nipro Renal Solutions is recalling Citric Complete Dry Citric Acid Concentrate due to high endotoxin levels. The product is used in hemodialysis.
Rivian is recalling 2022-2027 R1S, 2022-2026 R1T, and 2027 R2 vehicles because a notification may obstruct the rearview camera image, increasing crash risk.
Lutronic Corporation is recalling 1,065 DermaV Laser Systems because using higher fluences at 1064nm with current cryogen parameters may cause sparks or loud noise, potentially resulting in patient burns.
C.R. Bard is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
AVID Medical is recalling 98 Halyard IV Start Kits because wrinkles in the paper lidding may breach the seal, compromising sterility assurance.
Atrium Medical is recalling specific lots of Getinge PVC Thoracic Catheters because one lot failed bacterial endotoxin testing.
C.R. Bard is recalling SureStep Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
C.R. Bard is recalling 12,463 Foley and intermittent catheter trays because complaints indicated contamination on the surface of the included Pericare wipes.
C.R. Bard Inc. is recalling SureStep Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
Windstone Medical Packaging is recalling 3,260 AMS Convenience Kits because the included sodium chloride bags may contain detached blue break-off parts.
HeartSine Technologies is recalling SAM 350P, 360P, and 450P defibrillators due to a damaged membrane tail that causes intermittent faults.
Atrium Medical Corporation is recalling specific lots of Getinge PVC Thoracic Catheters because bacterial endotoxin testing results were out of specification.
L-Nutra Inc is recalling Prolon Everyday Apulian Almond & Cocoa Spread because it contains undeclared hazelnut, cashew, and pistachio.
Nipro Renal Solutions is recalling MedicaLyte Bicarbonate Powder due to high endotoxin levels. The recall affects 2,327 cases distributed in the US, Guatemala, and Panama.
Atrium Medical Corporation is recalling specific lots of Getinge PVC Thoracic Catheters because an out-of-specification result was found in bacterial endotoxin testing.
Ajanta Pharma USA Inc. is recalling Fluphenazine Hydrochloride tablets because testing revealed an organic impurity level slightly above the allowed limit.
C.R. Bard Inc. is recalling specific Bardex and SureStep Foley catheter trays because complaints indicated surface contamination on the included Pericare wipes.
C.R. Bard Inc is recalling specific Foley and Intermittent Catheter Trays because complaints indicated contamination on the surface of the included Pericare wipes.
OurPharma LLC is recalling 1,610 bags of fentanyl citrate injection solution due to a discrepancy between IV bag and product expiry dates.
ImprimisRx NJ LLC is voluntarily recalling 772 bottles of Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution because the drug is subpotent.
Grand Design is recalling 2026-2027 Lineage RVs with the optional 43 tire package because the vehicle's top speed may exceed the tire's rating, increasing crash risk.
Forest River is recalling 2024-2026 Rockport trucks because incorrectly routed wiring may contact the hood, causing a short circuit and increasing fire risk.
Micro Bird USA LLC is recalling 2025-2027 G5e school buses because a wiring harness may be incorrectly routed, potentially causing a loss of drive power and increasing crash risk.
Micro Bird is recalling 2025-2026 G5e transit buses because an incorrectly routed wiring harness may be damaged, causing a loss of drive power and increasing crash risk.
Volkswagen is recalling 2018-2021 Tiguan, Atlas, and Audi Q3 vehicles because a steering rack bolt may corrode and break, potentially causing loss of steering control.