State
72,913 recalls have nationwide distribution and so reach Florida. 12,818 additional recalls listed Florida specifically in their distribution scope.
Of the 12,818 recalls naming Florida we have scored against our rubric, 1,764 (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 12,818 recalls whose distribution notice names Florida specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BRP US Inc. recalls about 2,820 Can-Am Outlander Pro and Max Pro ATVs with defective Speed Limiter Mode that can cause unexpected speed and acceleration, posing a risk of serious injury or death from crashes.
Minka Lighting Group is recalling about 170 Bardon Series Pendant Light Fixtures because the frame can detach from the downrod during installation, posing a risk of serious injury or death. One detachment has been reported with no injuries yet.
Superbobi 7 3/8-inch pool drain covers violate federal safety standards and pose entrapment and drowning hazards. Pool owners should stop using affected covers immediately.
Hyundai is recalling certain 2024-2026 Elantra Hybrid vehicles because the hybrid power control unit assembly may overheat, increasing the risk of a fire. 54,337 vehicles are affected.
Petzl America is recalling about 29,300 climbing harnesses because the D-ring attachment point can release, creating a risk of serious injury or death from a fall.
BMW is recalling 2017-2018 C Evolution motorcycles because water splash can corrode electrical contacts, potentially causing overheating and fire.
Petzl America is recalling about 1,270 SIMBA and SWAN EASYFIT harnesses because missing rivets in the buckles can cause them to open, creating a risk of serious injury or death from falls.
ZWILLING J.A. Henckels has recalled approximately 113,440 ENFINIGY electric kettles in the U.S. because the handle can loosen and separate, causing hot water to spill and posing a burn injury risk.
Honda is recalling certain 2024-2025 Prologue and 2024 Acura ZDX vehicles because the rearview camera screen may display a distorted or blank image. 59,887 vehicles are affected.
Guangzhou Lichengbei Battery Technology Co., Ltd. (LiCB) has recalled about 94,000 CR2032 3V lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Ingestion can cause serious internal injuries, chemical burns, and death.
Amazon is recalling Amazon Basics 55 Lbs. Adjustable Dumbbells because weight plates can fail to engage completely and dislodge during use, posing an impact hazard. No injuries have been reported.
Cook Incorporated is recalling Centimeter Sizing Catheters because marker bands may crack or break, potentially causing device fragmentation, vessel injury, or life-threatening harm.
Cook Incorporated is recalling Aurous Centimeter Sizing Catheters due to risk of marker band cracking or breakage during angiographic procedures. Potential complications include device fragmentation, vessel injury, and in worst-case scenarios, life-threatening harm or death.
Raw Farm Original Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Intuitive Surgical is recalling Intuitive 8 mm SureForm 30 Gray Reloads (Reference Numbers 48230M-05 and 48230M-06) because they may produce an incomplete staple line during curved-tipped stapler operations.
AVID Medical is recalling the Halyard CATH LAB kit (Model SACL75-01) due to risk that a Medline syringe rotating adaptor may unwind during use, causing loose or complete disconnection between the syringe and manifold.
Raw Farm Shredded Raw Cheddar in 80 oz bulk format is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Raw Farm Raw Cheddar Original in 8 oz and 16 oz sizes is being recalled in connection with a multi-state outbreak of E. coli O157:H7.
Teva Pharmaceuticals USA, Inc. is recalling 2,200 kits of Octreotide Acetate for Injectable Suspension (30 mg) due to quality system deficiencies that affect sterility assurance. The recall affects all lots nationwide.
AVID Medical is recalling Halyard CARDIAC CATH PACK SAN23CARDQ kits (Model DRCC36) due to a Medline syringe rotating adapter that may unwind during use, potentially causing loose or full disconnection between the syringe and manifold.
French Broad Chocolate bette's bake sale bonbon assortments are being recalled because the printed tasting guide misidentifies the Walnut Fudge and Peach Cobbler chocolates.
Erbe Medical is recalling ERBEFLO 2 Endoscopy Pump Tubing/Cap Sets due to a connector design that may allow unintended water flow, potentially leading to water aspiration and serious respiratory conditions.
Medline Industries is recalling four Convenience Kit models (892 units) nationwide because sterilization and packaging equipment calibration issues may have compromised the sterility assurance level of the devices.
Erbe Medical is recalling ERBEFLO CleverCap CO2 hybrid tubing and cap sets used with endoscopes because the distal connector may allow unintended water flow, potentially leading to water aspiration and serious respiratory complications.
CareFusion 213, LLC is recalling BD PurPrep (povidone-iodine 8.3% with isopropyl alcohol 72.5%) due to lack of assurance of sterility and potential product contamination. Affected lots are distributed nationwide.