The Recall Desk

State

Florida product recalls

72,984 recalls have nationwide distribution and so reach Florida. 12,821 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,821
Critical
1,765
Severe
2,975
Most recent
2026-09-16

Of the 12,821 recalls naming Florida we have scored against our rubric, 1,765 (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 12,821 recalls whose distribution notice names Florida specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6501–6525 of 85805

  • HighFDA (Devices)·Z-2108-2025·2025-07-16

    Alcon Constellation vitrectomy packs may have damaged lidding compromising sterility

    Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.

    Product
    Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure Pak Model/Catalog Number: Many - See 'Attachment 1 - Affected Product List' Software Version: N/A Product Description: Surgical procedure pack to interface with Alcon Constella
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2091-2025·2025-07-16

    TrueDent Cyan dental resin cartridges carry an expiration date formatting error

    TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.

    Product
    TrueDent Cyan, TDM 120, Model No. OBJ-09165 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2025·2025-07-16

    In Your Face tinted mineral sunscreen recalled over manufacturing practice deviations

    In Your Face Mineral Tint SPF 31 tinted sunscreen is being recalled because of cGMP deviations. 76 bottles are affected.

    Product
    In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0513-2025·2025-07-16

    Erin's Faces mineral sunscreen recalled over manufacturing practice deviations

    Erin's Faces Mineral SPF 32 sunscreen is being recalled because of cGMP deviations. 54 tubes are affected.

    Product
    Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide, 3 FL OZ/ 85 mL per bottle, Made in USA for Erin's Faces, Millburn, NO 07041. NDC: 73369-1401-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2090-2025·2025-07-16

    TrueDent Clear dental resin cartridges carry an expiration date formatting error

    TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.

    Product
    TrueDent Clear, TDM 100, Model No. OBJ-09164 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2092-2025·2025-07-16

    TrueDent dental resin cartridges carry a formatting error in expiration dates

    TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.

    Product
    TrueDent Magenta, TDM130, Model No. OBJ-09166 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0514-2025·2025-07-16

    GreenScreen zinc oxide sunscreen recalled over manufacturing practice deviations

    GreenScreen organic zinc oxide sunscreen SPF 32 is being recalled because of cGMP deviations. 174 tubes are affected.

    Product
    GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide Sunscreen, Organic Ingredients, Fragrance Free, Biodegradable, Chemical Free, Non-Nano, Baby Safe, Original, SPF 32, Totally Green personal care, Zinc Oxide USP 25%, 3.4 FL OZ/115 G Tube, NDC: 73369-0001-1
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-2093-2025·2025-07-16

    TrueDent Yellow dental resin cartridges carry an expiration date formatting error

    TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.

    Product
    TrueDent Yellow, TDM140, Model No. OBJ-09169 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2094-2025·2025-07-16

    TrueDent White dental resin cartridges carry an expiration date formatting error

    TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.

    Product
    TrueDent White, TDM110, Model No. OBJ-09168 Light-curable methacrylate-based resin that enables fabrication of dental appliances
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2107-2025·2025-07-16

    Preat Astra dental analogs have rotational feature 180 degrees off

    Preat Astra EV-compatible 4.2 mm Digital Analogs are being recalled because a manufacturing error left the digital analog rotational feature 180 degrees off. 44 units are affected.

    Product
    Preat, Astra EV-compatible 4.2mm Digital Analog REF: 9006603 (single) and 9006603-10(10 pack), Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0512-2025·2025-07-16

    B Natural Organics mineral sunscreens recalled over manufacturing practice deviations

    B Natural Organics Organic Sunscreen SPF 30, in tinted and tint free formulas, is being recalled because of cGMP deviations. 204 tubes are affected.

    Product
    B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c)
    Category
    Drug
    Distribution
    3 states
  • ModerateFDA (Food)·H-0259-2025·2025-07-16

    Shoppers Value fruit cocktail recalled over undeclared Red No. 3 colour

    Shoppers Value Fruit Cocktail in heavy syrup is being recalled because of undeclared Red No. 3 (E127). 1,105 cases are affected.

    Product
    SHOPPERS VALUE FRUIT COCKTAIL in HEAVY SYRUP, Net Wt. 22.5lbs, 24/15 OZ Cans per case.
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Drugs)·D-0509-2025·2025-07-16

    Famciclovir tablets recalled after a hair was found on a tablet

    Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.

    Product
    FAMCICLOVIR — FAMCICLOVIR (FAMCICLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V415000·2025-07-15

    Porsche suspension strut retaining ring can loosen dislodging the strut

    Porsche is recalling certain 2025 Panamera, Panamera E-Hybrid and Taycan vehicles because a retaining ring on top of the suspension strut may come loose, dislodging the strut and losing air from the spring.

    Product
    PORSCHE — PORSCHE TAYCAN, PANAMERA, PANAMERA 4 E-HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V408000·2025-07-15

    Winnebago Recalls 2025 Micro Minnie Trailers Due to Cooktop Flame Inversion Risk

    Winnebago is recalling 2025 Micro Minnie and Micro Minnie FLX travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire risk.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE FLX, MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V468000·2025-07-14

    AMO Recalls 2025 Utility Trailers Due to Axle Separation Risk

    American Manufacturing Operations is recalling 2025 AMO Utility trailers because shackle nuts may loosen, allowing the axle to detach and increasing crash risk.

    Product
    AMO — AMO UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25E043000·2025-07-14

    Peragon Tectonic Tonneau Covers Recalled for Detachment Risk

    Peragon is recalling Tectonic hard tonneau covers because damaged plastic slides may allow the cover to detach during transit, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V420000·2025-07-14

    Polestar 3 panoramic glass sunroofs may not be properly secured

    Polestar is recalling certain 2025 Polestar 3 vehicles because the panoramic glass sunroof may not be properly secured and can detach. 33 vehicles are affected.

    Product
    POLESTAR — POLESTAR POLESTAR 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V459000·2025-07-11

    Zero Motorcycles Recalls 2024 Models Due to Front Brake Hose Defect

    Zero Motorcycles is recalling 2024 DSR/X, DS, DSR, and DSRP motorcycles because a twisted front brake hose may leak fluid and reduce braking ability.

    Product
    ZERO — ZERO DSRP, DSR, DS, DSR/X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V467000·2025-07-11

    Ford Bronco Sport and Escape fuel injectors may crack and leak

    Ford is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles with 1.5L engines because a fuel injector may crack and leak fuel inside the engine compartment. 694,271 vehicles affected.

    Product
    FORD — FORD BRONCO SPORT, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V463000·2025-07-11

    Mercedes-Benz Metris rearview camera image may fail to display

    Daimler Vans USA is recalling certain 2020-2023 Mercedes-Benz Metris vehicles because unsecured infotainment connections can stop the rearview camera image displaying. 43,422 vehicles affected.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V466000·2025-07-11

    Jaguar E-Pace passenger air bags may tear during deployment

    Jaguar is recalling certain 2021-2024 E-Pace vehicles because the passenger air bag may tear during deployment. 1,436 vehicles are affected.

    Product
    JAGUAR — JAGUAR E-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V464000·2025-07-11

    Forest River Recalls 2026 Westbrook and Tracer Trailers for LP Gas Hose Defect

    Forest River is recalling 2026 Westbrook and Tracer recreational trailers because a liquid propane gas hose may rub against the furnace, causing a fuel leak that increases fire risk.

    Product
    FOREST RIVER — FOREST RIVER WESTBROOK, TRACER
    Category
    Vehicle
    Distribution
    Distributed nationwide