The Recall Desk

State

Florida product recalls

72,940 recalls have nationwide distribution and so reach Florida. 12,818 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,818
Critical
1,764
Severe
2,975
Most recent
2026-09-09

Of the 12,818 recalls naming Florida we have scored against our rubric, 1,764 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,975 (23%) are Severe.

These figures cover only the 12,818 recalls whose distribution notice names Florida specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4451–4475 of 85758

  • HighFDA (Devices)·Z-0580-2026·2025-12-03

    Expandable spinal cages recalled because they may lose height or collapse

    Medtronic Sofamor Danek is recalling 275,260 Catalyft PL and PL40 expandable interbody spacers because the cage may lose height or collapse, risking migration or neurological injury.

    Product
    Catalyft PL & PL40 Expandable Interbody System labeled as follows with corresponding model numbers: 1. SPACER 6068073 CATALYFT PL SHORT 7MM. Model Number: 6068073. 2. SPACER 6068076 CATALYFT PL LONG 7MM, Model Number: 6068076. 3. SPACER 6068093 CATALYFT PL SHORT 9MM, Mo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2026·2025-12-03

    Heated massage tables recalled over heat components that can smolder

    Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: AMQ400H; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0594-2026·2025-12-03

    Diabetes clinic software recalled over incorrect sensor glucose graph data

    Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.

    Product
    CareLink Clinic, REF: MMT-7350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2026·2025-12-03

    Demonstration only gel recalled because it may be placed in patients

    Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.

    Product
    Emdogain; Article Numbers: (1) 440.230V10, (2) 475.132V10;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V836000·2025-12-03

    Volkswagen ID.4 recalled for high-voltage battery fire risk

    Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0589-2026·2025-12-03

    Vena cava filters recalled over resistance when advancing the dilator

    Argon Medical Devices is recalling 1,821 Option ELITE Vena Cava Filter Systems after complaints of increased resistance when advancing the dilator within the introducer sheath.

    Product
    Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava (IVC) in the following conditions: " Pulmonary t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0179-2026·2025-12-03

    Saline nasal spray recalled over microbial contamination with Pseudomonas lactis

    Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.

    Product
    Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0587-2026·2025-12-03

    Q400 massage tables recalled over heat components that can overheat

    Pivotal Health Solutions is recalling 34 Quantum Intersegmental Tables, model Q400, because damage to the heat function components can lead to overheating and smoldering.

    Product
    Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0599-2026·2025-12-03

    Myriad handpieces recalled because packaging tape contains undisclosed latex

    Stryker is recalling 39,148 NICO Myriad Handpieces because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO Myriad Handpiece Product Number/Product Name: NN-8000 15x10 MHP; NN-8001 15x 13 MHP; NN-8002 15x 25 MHP - MINOP; NN-8003 13x10 MHP; NN-8004 13x13 MHP; NN-8005 15x25 MHP GAAB; NN-8006 11X10 MHP; NN-8007 11x13 MHP; NN-8008 19x28 MHP OI; NN-8010 17x31.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0601-2026·2025-12-03

    Brain access devices recalled because packaging tape contains latex

    Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0583-2026·2025-12-03

    Skin cancer aid recalled because it may not meet specifications

    DermaSensor is recalling nine affected units of its software-aided diagnostic device because it may not meet specifications, risking incorrect results or a delayed referral.

    Product
    DermaSensor. Model/Catalog Number: 10101. Software Version: 3.0.2. Software-aided adjunctive diagnostic device for use by physicians on lesions suspicious for skin cancer
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0600-2026·2025-12-03

    Illumination packs recalled because packaging tape contains undisclosed latex

    Stryker is recalling 39,148 NICO Myriad Illumination Packs because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.

    Product
    NICO Myriad Illumination Pack Product No. NN-1000 11g Illumination Sleeve/Fiber; Product No. NN-1001 13g Illumination Sleeve/Fiber
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0722-2026·2025-12-03

    Hot and cold wraps recalled over microwave instructions causing burns

    DJO is recalling 1,594 Cold Form Wraps because the instructions tell users to microwave the wrap for three minutes, which may cause leaks or second degree burns.

    Product
    Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2026·2025-12-03

    IV set 490487 recalled over piggyback backflow and occlusion risk

    B. Braun Medical is recalling 23,160 units iv administration sets over the potential for medication backflow from secondary piggyback containers and an inability to prime.

    Product
    FoundationOne Liquid CDx (F1LCDx), TECH-0009 version 6.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0602-2026·2025-12-03

    Respiratory test panels recalled over elevated risk of false negative results

    BioFire Diagnostics is recalling 23 kits of the BioFire Respiratory Panel 2.1 because unintended movement of pouch chemistry may cause false negative results and control failures.

    Product
    BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0721-2026·2025-12-03

    Isoflurane vaporizers recalled over the potential for anesthesia leakage

    Mindray is recalling 54 Isoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.

    Product
    Isoflurane (ISO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Iso E_Vap. (Safety Filling adapter), Part Number 115-066758-00. 2. Exchange Iso E_Vap. (Safety Filling adapter), Part Number E115-066758-00. Product Description: The
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0584-2026·2025-12-03

    Blood lead test kits recalled over mislabeled calibration buttons

    Magellan Diagnostics is recalling 1,774 LeadCare II Blood Lead Test Kits because calibration buttons used in kitting were labelled with the wrong lot number.

    Product
    The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0723-2026·2025-12-03

    Imaging software recalled over a bug that can lose clinical information

    Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.

    Product
    IntelePACS - InteleConnect / TechPortal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0207-2026·2025-12-03

    Ice cream bars recalled over undeclared wheat and soy allergens

    Jeni's Splendid Ice Creams is recalling 3,767 cases of Passion Fruit Dreamsicle Ice Cream Bars over undeclared wheat and soy.

    Product
    Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 10850060644129
    Category
    Food
    Distribution
    10 states
  • ModerateFDA (Drugs)·D-0186-2026·2025-12-03

    Benzoyl peroxide cream recalled over current good manufacturing practice deviations

    CA Botana International is recalling 470 tubes of Doctor D. Schwab Controlling Cream with Benzoyl Peroxide 2.7% for CGMP deviations.

    Product
    Doctor D. Schwab Controlling Cream, Benzoyl Peroxide 2.7%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-017-05
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0185-2026·2025-12-03

    Tea tree balm recalled over current good manufacturing practice deviations

    CA Botana International is recalling 555 tubes of Doctor D. Schwab Controlling Balm with Tea Tree Oil for CGMP deviations.

    Product
    Doctor D. Schwab Controlling Balm with Tea Tree Oil, Salicyclic Acid 0.8%, 1 FL OZ/ 30 ML per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92123. NDC: 35192-016-05
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0192-2026·2025-12-03

    Tinted mineral sunscreen recalled over manufacturing practice deviations

    CA Botana International is recalling 2,090 tubes of Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 for CGMP deviations.

    Product
    Sugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0184-2026·2025-12-03

    Tinted moisturizer SPF 50 recalled over manufacturing practice deviations

    CA Botana International is recalling 1,401 tubes of Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50 for CGMP deviations.

    Product
    Doctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17
    Category
    Drug
    Distribution
    5 states
  • ModerateFDA (Drugs)·D-0189-2026·2025-12-03

    Shimmery sun lotion recalled over current good manufacturing practice deviations

    CA Botana International is recalling 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 for CGMP deviations.

    Product
    Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30, Titanium Dioxide 5% and Octinoxate 4%, 4 oz./113.4 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-012-02
    Category
    Drug
    Distribution
    5 states