State
20,322 recalls have nationwide distribution and so reach Florida. 0 additional recalls listed Florida specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Florida consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Medtronic is recalling 44 units of the Duet External Drainage and Monitoring system because the product labels contain an incorrect expiration date. The affected lot (226632942) was distributed nationwide.
Alembic Pharmaceuticals is recalling 82,400 bottles of Tobramycin Ophthalmic Solution nationwide because the product failed to meet impurities and degradation specifications.
PLUVICTO (lutetium Lu 177 vipivotide tetraxetan) injection vials were labeled with incorrect lot numbers and expiration dates. The manufacturer is recalling affected lots distributed nationwide.
Zipadee Kids Convertible House Bed Frames and Montessori Floor Beds are being recalled due to spindle spacing that can trap a child's torso while preventing their head from passing through, creating a strangulation hazard. At least two children have become entrapped.
Costco is recalling approximately 350,000 Ubio Labs power banks (model PWB1071) that can overheat and ignite. The company has received three fire reports, including one on a commercial flight with four smoke inhalation reports and one minor burn injury.
Simplay3 Toddler Towers can tip over during use, posing fall and injury hazards to young children. The manufacturer has received 16 reports of tipping, including 10 reports of injuries.
Midwest Lubricants is recalling about 3,000 units of Sodium Hydroxide (Caustic Soda Beads) because the packaging is not child-resistant and the label lacks required hazard information. The product poses a risk of chemical burns and eye irritation.
Gree is recalling approximately 1.56 million dehumidifiers sold under brand names including GE, Kenmore, SoleusAir, Seabreeze, and Norpole because they can overheat, smoke, and catch fire, creating fire and burn hazards.
ONO LLC is recalling ONO Vegan Blueberry Muffin Protein Overnight Oats because they contain undeclared milk, a common allergen. The product was distributed nationwide and poses a risk to consumers with milk allergies.
Cava Spicy Hummus (8oz, UPC 89832800227) is being recalled because it contains undeclared sesame. The product was distributed nationwide; consumers with sesame allergies may be at risk.
Betty Lou's Paleo Java Nuts About Energy Balls are being recalled due to undeclared sesame in the product. The recall affects packages distributed nationwide.
Olympus revised OER-Pro labeling because two endoscope models (LF-V, LF-P) are no longer compatible. Sterilization parameters and cleaning procedures have also changed.
LINK MP Monoblock hip stem trial instruments may require excessive force to remove after impaction, potentially prolonging surgery or requiring procedural modification.
Waldemar Link GmbH recalls LINK MP Monoblock hip stem trial instruments due to increased removal force requirements after impaction, which may prolong surgery or require procedural modification.
Siemens ARTIS icono floor angiography systems may experience thermal overload in cable connectors during fluoroscopy, causing burning smell and loss of imaging capability. The recall affects 7 units worldwide.
Philips MR 7700 MRI systems can have their smoke detector interlock safety mechanism bypassed when power cycled after smoke detection, allowing continued operation despite potential fire hazards.
Siemens has recalled 10 ARTIS angiography systems due to thermal overload hazard in cable connectors. The issue may cause burning smell and loss of imaging functionality, potentially requiring treatment cancellation or system replacement.
ORTHO-CLINICAL DIAGNOSTICS is recalling VITROS Troponin I ES Reagent Pack due to potential incorrect wells that could generate false negative diagnostic results. Lot 4800 with expiration 10-Jun-2023 is affected.
FDA recalls Randox RX Series Urea test kits because carryover from prior LDL-cholesterol tests may produce falsely low results, up to 11% below accurate values, potentially delaying diagnosis.
Waldemar Link GmbH recalled LINK MP Monoblock hip stem trial instruments (Size 23) nationwide due to increased force required for removal post-impaction, potentially prolonging surgery time.
Waldemar Link is recalling LINK MP Monoblock Hip Stem trial instruments due to increased force required for removal during surgery, which may prolong the procedure or require modification.
Olympus is updating labeling for 686 LF-P fiberscopes to clarify they are no longer compatible with OER reprocessors and specify new 100% ETO sterilization protocol.