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Recalls in Florida

Recalls sold in Florida, including nationwide recalls, newest first.
Agency
Risk level
Date
Sold in

21 recalls

Chevrolet Silverado 1500 (2016-2017), Chevrolet Silverado 2500 (2016), and 4 more

Air bag inflator end caps may detach or rupture, projecting fragments into the vehicle and increasing injury risk.

NHTSA, Air bag defect

Grand Design Reflection Fifth Wheel Recreational Trailers

The auto detect solar controller may select a 24 volt output when the system is designed for 12 volts, damaging circuits.

NHTSA, Electrical system defect

Cadillac OPTIQ Vehicles

The front windows may fail to reverse when closing, which can pinch a passenger.

NHTSA, Electrical system defect

Land Rover Defender (2024)

The second-row seat belt may be improperly stitched and fail to restrain an occupant during a crash.

NHTSA, Seat belt defect

Altec Digger Derrick (2021-2026) and Altec TA Series Aerial Device (2023-2025)

Improper wiring may prevent the boom stow auto-neutral feature from engaging, allowing the truck to be driven with the boom elevated.

NHTSA, Electrical system defect

OneBlood Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated

Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated were labeled as leukocytes reduced but were not tested to verify white blood cell count.

Moderate risk, FDA, Quality testing problem

11 recalls

Berlin Seeds Alfalfa Sprouting Seeds

Alfalfa sprouting seeds may be contaminated with E. coli and Salmonella, which can cause serious infections.

High risk, FDA, Salmonella

Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops

Clear Eyes Redness Relief eye drops lack assurance of sterility.

Moderate risk, FDA, Sterility problem

AVID Medical Halyard IV Start Kits

Halyard IV Start Kit NON-Sterile may have an open or incomplete seal on the applicator packaging.

Moderate risk, FDA, Packaging defect

AVID Medical Halyard IV Start Kits

Halyard IV Start Kit NON-Sterile may be contaminated with Aspergillus penicillioides.

High risk, FDA, Contamination

Cardioroot Woven Collagen Coated Vascular Graft

The Cardioroot Woven Collagen Coated Vascular Graft failed water permeability acceptance criteria.

Moderate risk, FDA, Device defect

Imager II Angiographic Catheters

Imager II Angiographic Catheters may fracture or detach, leading to device fragments remaining or migrating.

High risk, FDA, Device defect

Baxter Volara System

Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate.

Moderate risk, FDA, Contamination

Forest River Cedar Creek Fifth Wheel Recreational Trailers

The sleeper sofa in Cedar Creek fifth wheel trailers may block the bunkroom door, delaying exit in an emergency.

NHTSA, Vehicle structure defect

Land Rover Range Rover Sport

The Range Rover Sport has a powertrain control module that may be deformed, causing a loss of drive power.

NHTSA, Transmission or drivetrain defect

Forest River Dynamax Isata Recreational Vehicles

The bunk mat in these vehicles may be misaligned and unsupported, increasing injury risk.

NHTSA, Vehicle equipment defect

Forest River Dynamax Isata Recreational Vehicles

The bunk ladder may come loose from the mattress insert, increasing injury risk.

NHTSA, Vehicle equipment defect

10 recalls

A&D Foods Beef, Pork and Goat Cuts

Raw pork, beef, and goat products were produced without federal inspection and bear a false USDA mark of inspection, making them unsafe to eat.

High risk, FSIS, Produced without inspection

Macleods Olanzapine Tablets

Olanzapine Tablets, USP 5 mg, failed impurities and degradation specifications.

Low risk, FDA, Drug impurity

Amneal Exenatide Injection

Exenatide Injection prefilled pens may contain no medication due to a defective delivery system.

Moderate risk, FDA, Device defect

Cardinal Health 200 Presource Convenience Kits

Presource Convenience Kits contain applicators with open or incomplete seals, which could cause infection.

Moderate risk, FDA, Contamination

NGenuity Patient Monitor with Capnography (ETCO2)

The patient monitor can show a Checkline Error alarm at setup, which may delay the procedure.

Moderate risk, FDA, Device defect

Ford Service Parts 10.1 Inch Center Stack

The 10.1-inch center stack screens may lose power and fail to display the rearview camera image, reducing the driver's view and increasing crash risk.

NHTSA, Backup camera defect

Ford Ranger

The 2026 Ford Ranger's rearview camera image may not display, reducing the driver's view and increasing crash risk.

NHTSA, Backup camera defect

Nova Bus LFS (2024-2025)

The parking brake may activate unintentionally, causing the bus to suddenly slow or stop without brake lights.

NHTSA, Brake defect

Ford Expedition (2025-2027), Ford F-250 SD (2026), Ford F-350 SD (2026), and 2 more

The headlights may fail, reducing visibility and increasing crash risk.

NHTSA, Exterior lighting defect

Tissue Transplant Technology Bone

Bone products could cause contamination or spread of disease.

Moderate risk, FDA, Contamination

6 recalls

Niwali Tejocote Capsules and Niwali Tejocote Pieces

Niwali Tejocote Capsules and Pieces contain yellow oleander, which can cause severe or fatal health effects.

FDA

Sterling Pharmaceutical Services Lubricant Eye Drops and Ointments

AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% lacks assurance of sterility.

Moderate risk, FDA, Sterility problem

ForeSight Elite Tissue Oximetry Cable

The ForeSight Elite Tissue Oximetry Cable has incorrect switching of channels 1 and 2 on the module and flag labels.

Moderate risk, FDA, Labeling error

Forest River Dynamax Grand Sport GT Recreational Vehicles

The engine pre-heat pump may be improperly installed, causing coolant hose failure.

NHTSA, Fuel system defect

Abiomed Impella Controllers

The Automated Impella Controller has defects in firmware and software that can affect pressure signal accuracy and cause unreliable signals.

Moderate risk, FDA, Software defect

CorneaGen Cornea

Corneas, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant communicable disease agents and diseases, were distributed.

Moderate risk, FDA, Blood donor screening

13 recalls

Endo Dexmedetomidine HCl in 0.9% Sodium Chloride Injection

Dexmedetomidine HCL in 0.9% Sodium Chloride Injection contains particulate matter that can cause life-threatening health consequences.

High risk, FDA, Foreign object

Philips Achieva, Ingenia, Intera and MR MRI Systems

A software issue can terminate an examination during image reconstruction if scan parameters are manually adjusted.

Moderate risk, FDA, Software defect

Philips EPIQ Elite Diagnostic Ultrasound System

The Philips EPIQ Elite ultrasound system has a software issue that can cause inaccurate blood flow measurements and misdiagnosis.

Moderate risk, FDA, Software defect

Fresenius Medical Care CombiSet Hemodialysis Blood Tubing Sets

Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.

Moderate risk, FDA, Device defect

Maquet PowerLED 300 Concealed Lighting System

The PowerLED 300 Concealed Lighting System can detach at the junction between the spring arm and suspension arm and fall, causing potential injury.

Moderate risk, FDA, Device defect

SeaSpine Mariner Deformity Extended Polyaxial Head

The spinal device has a thread depth out of design specification.

Moderate risk, FDA, Device defect

HomeFill Oxygen Cylinders

Oxygen cylinders lack required medical gas labeling.

Moderate risk, FDA, Labeling error

CooperSurgical INCA Infant Nasal CPAP Sets

The INCA Infant Nasal CPAP Complete Set may have a loose tubing connection, causing loss of pressure and reduced oxygenation.

High risk, FDA, Device defect

Midmark IQvitals Zone

A performance issue may result in inaccurate blood pressure readings when the Linear Deflation Method is used.

Moderate risk, FDA, Device defect

Olympus BiCOAG Hemostasis Probe

The Olympus BiCOAG Hemostasis Probe may have a ceramic tip that can detach.

Moderate risk, FDA, Device defect

Winnebago Arka (2027)

Winnebago Arka recreational vehicles have an incorrect rear Gross Axle Weight Rating and cold tire inflation, which can cause tire overload and a crash.

NHTSA, Vehicle equipment defect

Volvo 9700 buses

Volvo 9700 buses have an emergency exit label missing operating instructions, which may delay exit and increase injury risk.

NHTSA, Vehicle equipment defect

REV: American Dream (2025-2026), Fleetwood Discovery LXE (2026-2027), Fleetwood Palisade (2026), and 1 more

The RoadWatch Safety System may be programmed with incorrect vehicle parameters, impairing electronic stability control.

NHTSA, Electrical system defect

21 recalls

Esjay Toddler Busy Board Montessori Toys

The toddler busy board toy has red knobs that can detach, posing a deadly choking hazard.

CPSC, Choking hazard

Friedrich KÜHL Q and KÜHL S Window Air Conditioners

The control board inside the motor of these air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards.

CPSC, Fire hazard

LANCHEZ Pressure Washers

Pressure washers lack a ground-fault circuit-interrupter and adequate power cord, posing shock and electrocution risks.

CPSC, Electric shock hazard

Melissa & Doug Lights & Sounds Fire Truck Activity Board

The fire truck activity board can detach, posing a choking hazard.

CPSC, Choking hazard