The Recall Desk

State

Florida product recalls

20,364 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.

13101–13125 of 20364

  • ModerateFDA (Drugs)·D-0791-2023·2023-06-07

    Cetrorelix Acetate Injectable Recalled Due to Manufacturing Deviations

    Akorn, Inc. recalls all lots of Cetrorelix Acetate for Injection due to manufacturing process deviations. The company went out of business and could not complete required stability testing.

    Product
    Cetrorelix Acetate for Injection, 0.25 mg, , One carton contains one packaged tray which contains: 1 vial with lyophilized powder for reconstitution, 1 pre-filled syringe with diluent, 1 20-gauge needle, 1 27-gauge needle, Sterile - For subcutaneous use only, Rx Only, Manufacture
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0788-2023·2023-06-07

    AK-POLY-BAC Ophthalmic Ointment Recall for Manufacturing Compliance Deviations

    Akorn, Inc. recalls all lots of AK-POLY-BAC ophthalmic ointment nationwide because the company ceased operations and could not complete required stability testing.

    Product
    AK-POLY-BAC (bacitracin Zinc and Polymyxin B Sulfate) Ophthalmic Ointment, 3.5g, Sterile, Rx Only, For Ophthalmic Use Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0787-2023·2023-06-07

    Azelastine Hydrochloride Nasal Spray Recalled Due to Manufacturing Deviations

    Akorn, Inc. is recalling all lots of Azelastine Hydrochloride Nasal Spray nationwide due to manufacturing process deviations. The firm ceased operations and could no longer conduct required stability studies.

    Product
    Azelastine Hydrochloride Nasal Spray, 0.15%, 105.5 mcg per spray, Rx Only, For Intranasal Use Only, Manufactured by: Hi-Tech Pharmacal Co., INC., Amityville, NY 11701. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0781-2023·2023-06-07

    Acetic Acid Otic Solution recalled due to manufacturing deviations and unverified stability

    Akorn is recalling all lots of Acetic Acid Otic Solution nationwide due to manufacturing practice deviations. The firm went out of business and could not complete stability studies required to verify the product remained safe and effective.

    Product
    Acetic Acid Otic Solution, 15 mL per bottle, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0824-2023·2023-06-07

    Akorn Lidocaine Oral Solution Recalled Due to Manufacturing Compliance Deviations

    Akorn Operating Company is recalling all lots of Lidocaine Hydrochloride Oral Topical Solution 2% distributed nationally because the firm ceased operations and could not complete required stability studies.

    Product
    Lidocaine Hydrochloride Oral Topical Solution, USP (Viscous) 2%, 100mL tubes, Rx Only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0801-2023·2023-06-07

    Docusate Liquid Drug Recalled Over Incomplete Stability Testing

    Akorn, Inc. is recalling all lots of DOCU LIQUID (docusate sodium) after the company ceased operations and could not complete mandatory stability testing required for FDA compliance.

    Product
    DOCU LIQUID (docusate sodium, 50 mg/5 mL), packaged in 473mL bottles and b)10mL Unit Dose cups, Distributed by: Akorn Operating Company, LLC., Gurnee, IL 60031. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0844-2023·2023-06-07

    Akorn Sodium Chloride Ophthalmic Ointment Recalled Due to Manufacturing Deviations

    Akorn Inc. is recalling all lots of Sodium Chloride Ophthalmic Ointment 5% nationwide due to manufacturing practice deviations. The company ceased operations and could not continue stability studies required to verify the product's safety and effectiveness.

    Product
    Sodium Chloride Ophthalmic Ointment, USP, 5%, 3.5g tubes, Manufactured by: Akorn Inc., Lake Forest, IL 60045. ALL NDCs
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1664-2023·2023-06-07

    VITROS Chemistry Calibrator Kit Cannot Calibrate Vancomycin Reagent

    Ortho-Clinical Diagnostics is recalling 132 units of VITROS Chemistry Calibrator Kit 11 with defective Assay Data Disk versions due to inability to calibrate vancomycin reagent, delaying laboratory testing.

    Product
    VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN) 50 with affected Assay Data Disk (ADD) for Data Release Versions (DRVs) 6215 through 6223. In vitro diagnostic -VITROS Chemistry Products Calibrator Kit 11 is used to calibrate the VITROS 5,1 FS/4600 Che
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V345000·2023-06-06

    Mitsubishi Outlander PHEV backup camera display failure recall

    Mitsubishi is recalling certain 2023 Outlander PHEV vehicles due to a software error in the in-vehicle infotainment system that prevents the backup camera image from displaying. This can reduce rear visibility, increasing the risk of a crash or injury.

    Product
    MITSUBISHI — 2023 MITSUBISHI OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V493000·2023-06-06

    2021 Porsche Cayenne steering column screw defect may cause loss of control

    Porsche is recalling 2021 Cayenne vehicles because the screw connecting the steering column to the steering box may fail, potentially detaching the steering column and causing loss of vehicle control.

    Product
    PORSCHE — 2021 PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V407000·2023-06-06

    Pierce Aerial Ladder Platform Stabilizer Beam Cracks Pose Instability Risk

    Pierce is recalling certain 2016-2022 Ascendant 107' and 110' Platforms with potentially cracked galvanized stabilizer beams that could cause instability when elevated, increasing injury risk.

    Product
    PIERCE — 2020 PIERCE LADDER AND PLATFORM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V492000·2023-06-06

    2021 Volkswagen Jetta Air Bag Control Module Welding Defect Recall

    Volkswagen is recalling 2020-2021 Jetta vehicles because the air bag control module was welded in an incorrect position. This can cause air bags to deploy improperly during a crash or deploy unexpectedly, increasing injury risk.

    Product
    VOLKSWAGEN — 2021 VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V348000·2023-06-05

    Airstream Travel Trailers: Manual Step May Collapse Due to Fastener Defect

    Airstream is recalling certain 2022-2023 travel trailers with manual steps that may collapse due to a fastener screw pulling through the washer, increasing the risk of injury.

    Product
    AIRSTREAM — 2022 AIRSTREAM FLYING CLOUD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V351000·2023-06-05

    2022 Lucid Air Display Wiring Harness May Disable Critical Safety Screens

    Lucid is recalling 2022 Air vehicles because the display wiring harness may not be secured properly, potentially disabling screens that show speedometer, gear selection, and warning lights.

    Product
    LUCID — 2022 LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V253000·2023-06-04

    2023 BMW X5 Head Restraints May Fail in Crash

    BMW is recalling approximately 235 certain 2023 X5 vehicles with defective second-row head restraints that may not properly restrain occupants during a crash, violating federal safety standards.

    Product
    BMW — 2023 BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V263000·2023-06-04

    Tesla Model 3 Speedometer Unit Display May Fail in Track Mode

    Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V306000·2023-06-04

    Tiffin Bus and Phaeton motorhomes recalled for fuel rail leakage and fire risk

    Tiffin Motorhomes is recalling 2017-2021 Bus and Phaeton vehicles due to fuel rail assembly defects that may leak, posing a fire risk. Owners should contact Tiffin customer service at 1-256-356-8661 for a free inspection.

    Product
    TIFFIN — 2021 TIFFIN BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V264000·2023-06-04

    2022 Tesla Model X: Missing Seat Reinforcement Bracket Safety Defect

    Tesla is recalling one 2022 Model X vehicle due to a missing body structure reinforcement bracket at the second-row seat. This failure to comply with federal seat restraint standards increases the risk of occupant injury in a crash.

    Product
    TESLA — 2022 TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V252000·2023-06-04

    2022–2023 Land Rover Range Rover Seat Frame Defect Recall

    Jaguar Land Rover North America is recalling certain 2022–2023 Land Rover Range Rover vehicles because the second-row left seat frame may have been insufficiently welded and may not adequately secure occupants during crashes or sudden braking.

    Product
    LAND ROVER — 2022 LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V221000·2023-06-03

    2021 Alfa Romeo Stelvio Side Curtain Air Bag May Fail to Deploy

    2021 Alfa Romeo Stelvio vehicles may have improperly crimped clamps in the side curtain air bag assembly, which can fail to deploy in a crash, increasing injury risk. Chrysler will replace the assemblies at no cost.

    Product
    ALFA ROMEO — 2021 ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V223000·2023-06-03

    2020-2021 Lincoln Aviator vehicles recalled for backup camera display failure

    Ford is recalling 2020-2021 Lincoln Aviator vehicles because the backup camera display may not show video feed, affecting rear visibility. Free software updates are available from Ford dealers.

    Product
    LINCOLN — 2020 LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V146000·2023-06-03

    2023 Triumph Bonneville T120 motorcycles recalled for brake disc detachment risk

    Triumph is recalling certain 2023 Bonneville T120 motorcycles because the left-hand side brake disc may detach, reducing brake performance and increasing crash risk. Dealers will install replacement parts free of charge.

    Product
    TRIUMPH — 2023 TRIUMPH BONNEVILLE T120
    Category
    Vehicle
    Distribution
    Distributed nationwide