The Recall Desk

State

Florida product recalls

73,366 recalls have nationwide distribution and so reach Florida. 12,858 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,858
Critical
1,775
Severe
3,453
Most recent
2026-10-07

Of the 12,858 recalls naming Florida we have scored against our rubric, 1,775 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,453 (27%) are Severe.

These figures cover only the 12,858 recalls whose distribution notice names Florida specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18426–18450 of 86224

  • HighFDA (Devices)·Z-1577-2023·2023-05-17

    STA Compact Max analyzer firmware bug causes inaccurate test results

    A firmware bug in Diagnostica Stago's STA Compact Max analyzer causes intermittent shortened coagulation times and frequent technical errors that produce inaccurate lab test results. Five units were distributed to clinical laboratories nationwide.

    Product
    STA Compact Max fully automatic clinical analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0830-2023·2023-05-17

    Ziyad Cinnamon Powder Recalled for Elevated Lead Levels

    ZB Importing LLC is recalling Ziyad cinnamon powder (4.5 oz jars) from lot 21321G2 due to elevated lead levels. The recall affects 3,456 units distributed across multiple U.S. states and territories.

    Product
    Ziyad cinnamon powder, retail 4.5oz plastic jar with shaker cap UPC 074265007432, 12 retail jars per wholesale case
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1575-2023·2023-05-17

    STA R Max Analyzer Firmware Bug Produces Inaccurate Coagulation Test Results

    Diagnostica Stago is recalling the STA R Max fully automatic clinical analyzer due to a firmware bug that causes intermittent shortened coagulation times and increased technical errors, potentially producing inaccurate blood clotting test results.

    Product
    STA R Max fully automatic clinical instrument designed to perform tests on human plasmas, Reference Numbers 59013 and 59026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2023·2023-05-17

    APLS IgM Diagnostic Reagent Packs Recalled Due to Incorrect Conjugate

    Bio-Rad Laboratories is recalling 932 BioPlex 2200 APLS IgM Reagent Packs (Lot 301538) nationwide because they were packaged with incorrect conjugate. This could result in false-positive and false-negative test results.

    Product
    BioPlex 2200 REF 665-2050, APLS IgM Pack, APLS IgM Reagent Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2023·2023-05-17

    BD Pyxis MedStation ES software failure causes patient data loss

    BD Pyxis automated dispensing cabinet software versions 1.7.0 through 1.7.4 experience download failures causing partial loss of patient information and transaction data. This may result in dispensing incorrect medication doses, allergenic medications, or discontinued medications.

    Product
    BD Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES (Med ES Main Tower), REF: 352; BD Pyxis Anesthesia Station ES, REF: 327; BD Pyxis CII Safe ES Tower Main, REF: 1116-00; BD Pyxis CII Safe ES, Desktop PC, W-LESS SCNR, BIO, REF: 107-255-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1576-2023·2023-05-17

    STA Compact Analyzer Firmware Bug Causes Inaccurate Test Results

    Diagnostica Stago is recalling STA Compact Analyzers due to a firmware bug causing intermittent shortened coagulation times and increased technical errors. No illnesses or injuries have been reported.

    Product
    STA Compact Automated Multi-Parametric Analyzer, Reference Numbers 58602 and 58612
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0882-2023·2023-05-17

    Smoked Wahoo Dip Recalled Due to Undeclared Yellow #5 Allergen

    Borris Brothers is recalling Smoked Wahoo Dip due to undeclared Yellow #5 (tartrazine), an allergen that may affect consumers with sensitivity. The recall affects 112 containers distributed in Florida.

    Product
    Smoked Wahoo Dip, Net Wt. 8oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1569-2023·2023-05-17

    Aesculap Caiman Articulating Surgical Device Recalled for Loose Spring

    Aesculap Caiman Articulating electrosurgical devices are being recalled because a spring may become loose and fall out during surgery, potentially entering the patient's body.

    Product
    Aesculap Caiman Articulating D5/360MM - An electrosurgical cutting and coagulation device for cutting/coagulation/ablation during endoscopic (including laparoscopic, arthroscopic) surgery, and may in addition be intended for open surgery. Product Code: PL771SU
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0822-2023·2023-05-17

    Dr. Rico Perez Super Kids Colostrum Dietary Supplement Recalled for Undeclared Milk Allergen

    Dr. Rico Perez Super Kids Colostrum chewable tablets are being recalled because the product contains milk but does not declare this allergen on the label. Consumers with milk allergies may be at risk.

    Product
    Dr. Rico Perez Super Kids Colostrum, 60 count chewable tablets dietary supplement, Supplement Facts: 200 mg Colostrum per 1 tablet. HDPE bottle. UPC 8 79840 00044 6. Mfg For: Rico Perez Prod., In2295 Coral Way, Miami, FL 33145.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0883-2023·2023-05-17

    Smoked Swordfish Dip Recalled for Undeclared Yellow #5 Color Additive

    Borris Brothers voluntarily recalls 55 containers of Smoked Swordfish Dip (8oz) distributed in Florida due to undeclared Yellow #5, a color additive that can trigger reactions in sensitive individuals.

    Product
    Smoked Swordfish Dip, Net Wt. 8oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1573-2023·2023-05-17

    Laboratory Management Software May Display Incorrect Slide Labels

    TDHisto/Cyto laboratory management software may display incorrect information on slide labels in specific use cases. The FDA has issued a Class II recall affecting laboratories nationwide in California.

    Product
    TDHisto/Cyto - A software product used for managing medical information in the field of laboratories performing histology, nongynecological and gynecological cytology and autopsy activities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2023·2023-05-17

    M-Close Kit suturing apparatus recalled due to plastic housing fracture risk

    New Wave Endo-Surgical is recalling the M-Close Kit surgical suturing apparatus because the plastic housing may fracture. The recall affects 295 units distributed in Florida, Massachusetts, and Georgia.

    Product
    M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0881-2023·2023-05-17

    Food recall: Smoked Mahi Dip undeclared Yellow #5 additive

    Borris Brothers voluntarily recalled Smoked Mahi Dip (8oz and 48oz) in Florida due to undeclared Yellow #5 food dye. Consumers sensitive to this color additive should not consume the product.

    Product
    Smoked Mahi Dip, Net Wt. 8oz and 48oz
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0570-2023·2023-05-17

    Gabapentin tablets recalled due to product mixup with foreign tablet

    The Harvard Drug Group recalled 3,984 cartons of Gabapentin 600 mg tablets distributed nationwide due to a product mixup where one foreign tablet was found.

    Product
    GABAPENTIN — GABAPENTIN (GABAPENTIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0568-2023·2023-05-17

    Calcitonin Salmon Nasal Spray Recalled for Glass Particle Defect

    Apotex Corp. recalls Calcitonin Salmon nasal spray (82,375 bottles) nationwide due to a glass splinter entrapped in the pump mechanism. The defect renders the nasal spray inoperable.

    Product
    CALCITONIN SALMON — CALCITONIN SALMON (CALCITONIN SALMON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V346000·2023-05-16

    Dennis Eagle Recalls 2020-2023 ProView Vehicles for Short Seat Belts

    Dennis Eagle is recalling 2020-2023 ProView vehicles because the driver's seat belt is too short and difficult to buckle, increasing injury risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE PROVIEW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V348000·2023-05-16

    Western Star 57X Recalled for Turn Signal Software Defect

    Daimler Trucks North America is recalling 2023 Western Star 57X vehicles because interior turn signals may flash too quickly, potentially masking burnt-out exterior bulbs and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 57X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V347000·2023-05-16

    2020-2022 Porsche Taycan Brake Warning Indicator Defect Recall

    Porsche is recalling 2020-2022 Taycan vehicles because the brake pad wear warning indicator displays an incorrect color, potentially causing drivers to misinterpret the warning and drive on worn brake pads with reduced braking performance.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V344000·2023-05-12

    2023 Ford F-250, F-350, F-450 Super Duty Steering Column May Separate

    Ford is recalling certain 2023 F-250, F-350, and F-450 Super Duty vehicles due to loose or missing steering column bolts that could cause steering column separation, increasing the risk of crashes due to loss of steering control.

    Product
    FORD — FORD F-350 SD, F-250 SD, F-450 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V341000·2023-05-12

    Forest River Recalls 2022-2023 Rockport Work Trucks for Brake Wiring

    Forest River is recalling 2022-2023 Rockport work trucks because the trailer brake controller may be incorrectly wired, which can cause a loss of brake function and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V343000·2023-05-12

    Fox Factory Recalls Winch Remotes on 2021-2023 Jeep, GM, Ford, RAM Vehicles

    Fox Factory is recalling 1,578 vehicles equipped with Warn winches because water may enter the remote, corrode the circuit board, and cause the winch to operate unintentionally.

    Product
    FOX FACTORY — FOX FACTORY FORD PICKUP, GM PICKUP, RAM PICKUP, JEEP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V342000·2023-05-12

    2020-2023 Ford Explorer and Lincoln Vehicles Rearview Camera Failure

    The rearview camera video output may fail on certain 2020-2023 Ford Explorer and Lincoln vehicles, reducing rear visibility and increasing crash risk. Ford will replace the camera free of charge.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23201·2023-05-11

    Peloton Exercise Bikes Recalled for Seat Post Breakage and Fall Risk

    Peloton is recalling approximately 2.2 million Model PL01 exercise bikes because the seat post assembly can break during use, causing users to fall. The company has received 35 reports of seat post breakage, including 13 reports of injuries such as fractured wrists, lacerations, and bruises.

    Product
    Peloton Bikes Model PL01
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V338000·2023-05-11

    Jeep Cherokee Recall: Power Liftgate Electrical Short Fire Risk

    Chrysler is recalling 2014-2016 Jeep Cherokee vehicles with power liftgates due to an electrical short that may cause a fire. Owners should park outside until repairs are completed.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide