The Recall Desk

State

Florida product recalls

73,576 recalls have nationwide distribution and so reach Florida. 12,867 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,867
Critical
1,775
Severe
3,456
Most recent
2026-10-21

Of the 12,867 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 3,456 (27%) are Severe.

Which agencies issued them

These figures cover only the 12,867 recalls whose distribution notice names Florida specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

351–375 of 86443

  • ModerateFDA (Devices)·Z-0052-2027·2026-10-07

    FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 18" 1 LINE (10) Model/Catalog Number: DT-7018-01Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3318-2026·2026-10-07

    Philips MRI Systems Recalled for Incorrect Diffusion Tensor Imaging Data Exports

    Philips is recalling 91 Evolution MRI systems because Enhanced MR DICOM exports contain incorrect diffusion directions, preventing correct tractography reconstruction.

    Product
    Evolution upgrade 1.5T amd Evolution upgrade 3.0T; Model number (REF): 1. 782116 (1.5T), 2. 782148 (1.5T), 3. 782166 (1.5T), 4. 782201(1.5T), 5. 782117 (3.0T), 6. 782143 (3.0T), 7. 782162 (3.0T); Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3309-2026·2026-10-07

    Philips Ingenia MRI Systems Recalled for Incorrect DTI Data Exports

    Philips is recalling Ingenia 3.0T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.

    Product
    Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T CX); Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0013-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 10) WHITE Model/Catalog Number: 564011 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0046-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34" X 4" 2-Line, Blue Model/Catalog Number: ASP-564013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0058-2027·2026-10-07

    Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 2 LINE (10) Model/Catalog Number: DT-7034-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3313-2026·2026-10-07

    Philips MR 7700 MRI Systems Recalled for Incorrect DTI Data Exports

    Philips is recalling 107 MR 7700 MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing accurate tractography reconstruction.

    Product
    MR 7700; Model number (REF): 1. 782120, 2. 782153, 3. 782155, 4. 782199; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0056-2027·2026-10-07

    MPR Single Use Tourniquet Cuff Recalled for Incorrect Expiration Date

    ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3326-2026·2026-10-07

    Micro Therapeutics Recalls Pipeline Flex Embolization Device Due to Labeling Error

    Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm.

    Product
    Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex Embolization Device with Shield Technology consists of a permanent implant combined with a guidewire based delivery system. The Pipeline Flex Embolization…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0004-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number: 553323 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0063-2027·2026-10-07

    Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE (10) Model/Catalog Number: DT-7112-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0065-2027·2026-10-07

    ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE (10) Model/Catalog Number: DT-7115-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0029-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-LINE (CS 18) YELLOW Model/Catalog Number: A70107008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3317-2026·2026-10-07

    Philips MR 7700 Software Upgrade Recalled for Incorrect DTI Data

    Philips is recalling 30 MR 7700 software upgrades because they export incorrect diffusion tensor imaging data, preventing accurate nerve fiber mapping.

    Product
    Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3270-2026·2026-10-07

    HeartSine Defibrillators Recalled for Missing Maintenance Supplement

    HeartSine Technologies is recalling 31,834 public access defibrillators distributed without the required Maintenance Supplement, which describes an extra check every 3 months.

    Product
    HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3333-2026·2026-10-07

    Karl Storz Recalls HOPKINS Telescope Eyepieces Due to Labeling Error

    Karl Storz Endoscopy is recalling six HOPKINS Telescope eyepieces because of incorrect inside packaging labels. The units were distributed in Arizona, California, and Missouri.

    Product
    HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V656000·2026-10-06

    Great Dane Recalls 2027 Champion Trailers Due to Coupler Defect

    Great Dane is recalling 2027 Champion dry van trailers because an incorrect coupler plate may prevent proper coupling, increasing crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V655000·2026-10-06

    Ford Recalls 2025-2027 F-150 Trucks Due to Improperly Secured Front Seats

    Ford is recalling 2025-2027 F-150 vehicles because front seats may be improperly secured, increasing injury risk in a crash. Dealers will inspect and repair the seats free of charge.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V652000·2026-10-06

    E-One Recalls Fire Trucks Due to Wiring Overheat Risk

    E-One is recalling specific Typhoon N, Cyclone N, and Cyclone II fire trucks because a loose power supply may cause wiring to overheat, increasing fire risk.

    Product
    E-ONE — E-ONE CYCLONE N, TYPHOON N, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V657000·2026-10-06

    KME Recalls 2024 CV515 SFA 4x4 and Severe Service Emergency Vehicles

    KME is recalling 2024 CV515 SFA 4x4 and Severe Service emergency vehicles because a node may become unresponsive, causing loss of exterior lighting and pump-mode functionality.

    Product
    KME — KME CV515 SFA 4X4, SEVERE SERVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V654000·2026-10-06

    Spartan Fire Recalls One 2024 Metrostar Emergency Vehicle for Node Defect

    Spartan Fire is recalling one 2024 Metrostar emergency vehicle because a node may become unresponsive, causing loss of exterior lighting or pump-mode functionality.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide