State
72,992 recalls have nationwide distribution and so reach Florida. 12,823 additional recalls listed Florida specifically in their distribution scope.
Of the 12,823 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 2,977 (23%) are Severe.
Which agencies issued them
These figures cover only the 12,823 recalls whose distribution notice names Florida specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cargill Kitchen Solutions is recalling approximately 212,268 pounds of liquid egg products that may contain a cleaning solution with sodium hypochlorite.
Chrysler is recalling 2025 Pacifica Plug-In Hybrids because improperly tightened front brake caliper bolts may cause brake failure and reduced steering control.
Honda is recalling certain 2024-2025 ADV160 scooters because the oil pump driven gear may fail, resulting in a loss of drive power.
Oshkosh is recalling 2024-2025 NGDV vehicles because loose wiper arm nuts may cause wiper failure, reducing driver visibility and increasing crash risk.
BMW is recalling 2024-2025 M 1000 R and M 1000 XR motorcycles because a loose valve pin in the steering damper may cause increased steering effort and loss of control.
Specialized Vado and Como IGH e-bikes have defective chain/belt guards that do not fully cover the belt drive, allowing loose clothing to become entrapped and cause falls. About 32,400 units were sold in the US.
APOTHEKE's Pumpkin Ginger 3-wick candles can overheat and break their glass containers, posing fire and burn hazards. About 640 units were sold at Crate & Barrel from June 2024 through January 2025.
Interior Resources recalls approximately 1,772 children's steel utility bunk beds due to spacing violations that pose entrapment and strangulation hazards. No injuries have been reported.
About 17,660 NFH iron dietary supplement bottles lack child-resistant packaging required by federal law, posing a poisoning risk to young children. No injuries have been reported.
LINKCOO blackout roller window shades sold on Amazon from December 2022 through September 2024 are recalled due to long operating cords that pose strangulation and entanglement hazards to children.
George Oliver wooden dressers sold on Wayfair.com are unstable without proper wall anchoring, posing tip-over and entrapment hazards. About 220 units were sold; no injuries reported.
LaRose Industries is recalling about 224,100 Cra-Z-Art Gemex and Gel2Gem jewelry kits because the resin liquid can cause skin, eye, and respiratory irritation in children when inhaled, touched, or ingested.
General Motors is recalling certain 2025 Cadillac LYRIQ vehicles because the owner's manual inaccurately describes the rear outboard head restraints, failing FMVSS 202.
Vitality male enhancement dietary supplement recalled nationwide. Product contains undeclared prescription drugs sildenafil and tadalafil not disclosed to consumers.
Amgen recalls 258,750 vials of Neupogen (filgrastim) injection due to stability concerns. Stability data shows products may be out of specification at expiration; patients should consult healthcare providers about affected lots.
American Contract Systems Inc is recalling 1,200 DR DIULUS Injection Pack kits because the manufacturer cannot confirm sterilization assurance requirements were met. This may result in loss of functionality and treatment delays.
American Contract Systems Inc is recalling 144 CYSTO Model SACY80R kits due to inability to confirm sterilization requirements were met. Unsterilized devices may lose functionality and delay patient treatment.
Slate Run Pharmaceuticals is recalling Cinacalcet Hydrochloride Tablets 60 mg for containing nitrosamine impurity above acceptable daily intake limits. The recall affects 2,444 bottles distributed nationwide.
American Contract Systems Inc is recalling 237 laparoscopy surgical packs because sterilization assurance could not be confirmed. The packs may experience loss of functionality and require treatment delays.
Medline Industries is recalling 114 units of Proxima Drape surgical drapes due to a potential breach in pouch packaging that could compromise sterility. Affected units were distributed nationwide.
American Contract Systems is recalling PICC line catheters because sterilization assurance requirements could not be confirmed. Unsterilized devices may lose functionality and delay patient treatment.
Oridion Medical's CO2 sampling and airway adapter devices may be difficult to disconnect from endotracheal tubes, potentially causing treatment delays and serious respiratory complications in neonatal, infant, and pediatric patients.
American Contract Systems unable to confirm sterilization of 956 General Angio Pack kits distributed nationwide. Unsterile devices may lose functionality and delay patient treatment.
FUJIFILM's Synapse PACS Software versions 7.4.x incorrectly calculates patient age for infants under 3 months, potentially affecting clinical decisions. 104 units recalled in US and internationally.
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer (206 units) because an encoder wheel misalignment on the motor shaft can cause the instrument to stop and delay patient test results.