State

Florida product recalls

20,371 recalls have nationwide distribution and so reach Florida. 0 additional recalls listed Florida specifically in their distribution scope.

About recalls in Florida

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.

14851–14875 of 20371

HighFDA (Devices)·Z-0754-2023·2022-12-28
Vivid S5 N Ultrasound Systems Recalled for Potential Battery Fire Hazard
GE Medical Systems recalled 1,400 Vivid S5 N ultrasound systems for batteries that may fail, emit smoke, or catch fire if not replaced every 2 years as recommended.
Product
Vivid S5 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0752-2023·2022-12-28
GE Vivid S5 Ultrasound Systems Battery Failure Fire Risk
GE Medical Systems is recalling Vivid S5 ultrasound systems because batteries may fail if not replaced at the recommended 2-year intervals, potentially causing smoke or fire.
Product
Vivid S5 Ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and Superf
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0735-2023·2022-12-28
Natus Cranial Access Kit Recalled Due to Defective Sterile Surgical Drapes
Natus Medical is recalling 249 Cranial Access Kits distributed nationwide. The sterile surgical drape liners are difficult to remove without damage, potentially rendering the kits unusable for neurosurgical procedures.
Product
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set that is used to create an intracranial burr-hole typically required for procedures such as ventriculostomy or intracranial pressure (ICP) monitoring. The various
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0457-2023·2022-12-28
SurfaceSoap UV Disinfecting Wand Recalled for Excessive Ultraviolet Radiation
PhoneSoap has recalled its SurfaceSoap UV Disinfecting Wand due to excessive ultraviolet-C radiation emission. Approximately 6,700 units distributed nationwide may pose a radiation hazard to users.
Product
The product is a handheld ultraviolet-C germicidal wand and contains narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2023·2022-12-28
Baxter Revaclear 300 Dialyzers Recalled for Polyurethane Displacement
Baxter is recalling approximately 14 million units of Revaclear 300 dialyzers worldwide due to polyurethane displacement that could cause blood leaks. No injuries have been reported.
Product
Revaclear 300 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0755-2023·2022-12-28
GE Vivid S6 N Ultrasound Battery Fire Risk Recall
GE Vivid S6 N ultrasound systems may experience battery failure, smoke, or fire if batteries are not replaced every 2 years as recommended. Clinicians should replace batteries per manufacturer Service Manual instructions.
Product
Vivid S6 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0725-2023·2022-12-28
Intradental periodontal picks recalled for mislabeling by Young Dental
Young Dental Manufacturing has recalled Denticator PICK-A-DENT intradental picks due to mislabeling. The recall affects 600 packs distributed in Iowa, New York, Pennsylvania, Tennessee, Texas, and Canada.
Product
Denticator PICK-A-DENT, periodontal aid - intradental pick, REF 621714
Category
Medical Device
Distribution
Distributed nationwide
CriticalCPSC·23078·2022-12-22
Target Recalls Pillowfort Weighted Blankets Due to Asphyxiation Risk
Target is recalling about 204,000 Pillowfort Weighted Blankets because children can become entrapped inside the blanket cover, creating a risk of asphyxiation. Two children have died from this hazard.
Product
Pillowfort™ Weighted Blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·23080·2022-12-22
Samsung Top-Load Washing Machines Recalled for Fire Hazard
Samsung has recalled about 663,500 top-load washing machines because the machines can short-circuit and overheat, posing a fire hazard. A free software update is available to resolve the issue.
Product
Samsung Top-Load Washing Machines
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23081·2022-12-22
Nova Medical Home Bed Rails Recalled Due to Entrapment and Asphyxia Risk
Nova Medical Products is recalling approximately 20,000 Home Bed Rails (Models 6093 and 6094) because users can become entrapped within the bed rail or between the rail and mattress, posing a serious risk of death by asphyxiation.
Product
Home Bed Rails
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·23075·2022-12-22
GASGAS Off-Road Motorcycles Recalled for Engine Failure and Crash Hazards
KTM North America is recalling about 231 GASGAS MC 250 motorcycles due to an incorrectly programmed CDI box that can cause engine failure and pose crash and injury hazards. Consumers should stop riding the motorcycles immediately and contact an authorized dealer for a free repair.
Product
GASGAS Off-Road Motorcycles
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·23077·2022-12-22
Pacific 20-Inch Kids' Bicycles Recalled for Loose Handlebar Fall Hazard
Pacific Cycle is recalling about 147,000 Pacific Igniter and Pacific Bubble Pop 20-inch bicycles sold at Target because the handlebars can become loose during use, posing a fall hazard. Ten injuries involving bruising and abrasions have been reported.
Product
Pacific Igniter and Pacific Bubble Pop 20" kids' bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·23076·2022-12-22
BLU3 Nomad Battery-Powered Tankless Diving Systems Recalled for Drowning Hazard
BLU3 is recalling about 1,300 Nomad battery-powered tankless diving systems because the compressor head can fracture during use, restricting airflow and posing a drowning hazard to divers. No injuries have been reported.
Product
Nomad Battery-Powered Tankless Diving Systems
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0080-2023·2022-12-21
FDA Recalls Sodium Bicarbonate Injection Vials for Glass Breakage Risk
Exela Pharma Sciences is recalling Sodium Bicarbonate Injection vials due to defective containers that may break and release glass fragments when pressurized during preparation. The recall affects 37,320 vials distributed nationwide.
Product
8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0079-2023·2022-12-21
FDA Recalls Sodium Bicarbonate Injection for Defective Vials
Exela Pharma Sciences is recalling 489,600 vials of sodium bicarbonate injection nationwide due to defective vials that break and release glass fragments when pressurized during preparation.
Product
SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0489-2023·2022-12-21
Surgical dental procedure kits recalled due to incomplete bag sealing
Stradis Healthcare is recalling surgical and dental procedure kits due to manufacturing defects that may result in incomplete outer bag sealing and compromised sterility.
Product
STRADIS HEALTHCARE, Surgical Pk, Item No.40649ECS, dental
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0553-2023·2022-12-21
STRADIS HEALTHCARE Surgical Procedure Trays Recalled for Incomplete Sterile Sealing
STRADIS HEALTHCARE surgical procedure trays and kits are being recalled due to a manufacturing condition that may result in incomplete sealing of the outer bag, potentially compromising kit sterility.
Product
STRADIS HEALTHCARE, Femoral, Vasc, Item No.686-142,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0468-2023·2022-12-21
Zimmer Recalls NexGen Stemmed Tibial Components Due to Higher Revision Rates
Zimmer Inc. is recalling NexGen Option Stemmed Tibial Components due to clinically and statistically significant higher revision rates when used with specific femoral components. The components are being removed from inventory.
Product
NexGen Option Stemmed Tibial Component Size 5, Item Number 00-5986-047-01
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0550-2023·2022-12-21
Stradis Healthcare Endo Pack Surgical Trays Recalled for Incomplete Seal
Stradis Healthcare is recalling Endo Pack surgical trays (Item 682-509) because manufacturing defects may result in incompletely sealed outer bags, potentially compromising kit sterility. Products were distributed in the US and Canada.
Product
STRADIS HEALTHCARE, Endo Pack, Item No.682-509,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2023·2022-12-21
Surgical Trays Recalled Due to Incomplete Bag Sealing and Potential Loss of Sterility
Stradis Medical recalls surgical trays with incomplete outer bag seals that may breach kit sterility. No illnesses or injuries reported.
Product
Surgical room, SURGICAL PACK, Item No.40996WLS, oral surgery tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0469-2023·2022-12-21
Zimmer NexGen Option Stemmed Tibial Component Voluntary Recall Due to Higher Revision Rates
Zimmer is recalling NexGen Option Stemmed Tibial Components due to clinically significant higher revision rates when used with specific femoral components. Patients should contact their surgeon to discuss their implant.
Product
NexGen Option Stemmed Tibial Component Size 6, Item Number 00-5986-047-02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0532-2023·2022-12-21
FDA recalls Henry Schein bone marrow kit for defective seal
Henry Schein bone marrow kits may have incompletely sealed outer bags, compromising sterility. Affected units were distributed in the US and Canada.
Product
HENRY SCHEIN, BONE MARROW KIT, Item No.570-3092
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0524-2023·2022-12-21
Stradis Healthcare Surgical Knee Packs Recalled for Incomplete Sealing
HENRY SCHEIN Knee Packs are being recalled due to incomplete outer bag sealing that may breach sterility. Affected surgical kits were distributed in the US and Canada.
Product
HENRY SCHEIN, Knee Pack, Item No.570-2908,
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0474-2023·2022-12-21
Electrosurgical Suction Coagulator Devices Recalled Due to Potential Suction Port Blockage
ConMed's electrosurgical suction coagulator devices may have blocked suction ports that prevent proper function during procedures. Affected devices could cause procedure delays and require alternative equipment.
Product
Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction Coagulator 10FR, Catalog Number 130187
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0717-2023·2022-12-21
Diagnostic Kit Recall: Falsely Elevated Mold Allergen Test Results
Siemens IMMULITE 2000 allergen testing kits may produce falsely elevated results for mold allergen-specific IgE, potentially leading to incorrect mold allergy diagnoses.
Product
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS, except Japan Siemens Material Number (SMN): 10380875 For the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE mediated allergic disorders.
Category
Medical Device
Distribution
Distributed nationwide