The Recall Desk

State

Florida product recalls

73,584 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
1,771
Severe
3,460
Most recent
2026-10-21

Of the 12,867 recalls naming Florida we have scored against our rubric, 1,771 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 3,460 (27%) are Severe.

These figures cover only the 12,867 recalls whose distribution notice names Florida specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1001–1025 of 86451

  • HighFDA (Food)·H-1231-2026·2026-08-26

    Nutrient Foods Recalls Protein Cereal Cocoa Crunch for Undeclared Soy

    Nutrient Foods, LLC is recalling 16 kits of Protein Cereal Cocoa Crunch because soy was not declared in the contains statement.

    Product
    Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow pouch. Net wt.8.9 oz (252g). 1 pillow pouch per kit. Nutrient, 110 Woodland Ave Reno, NV 89523. No UPC Not for individual retail sale
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2964-2026·2026-08-26

    AVID Medical Recalls Halyard LAVH PACK Due to Sterilization Error

    AVID Medical, Inc. is recalling 40 packs of Halyard LAVH PACK kits because a component was improperly sterilized, potentially causing leaks.

    Product
    Halyard LAVH PACK, Model/Catalog Number: USAR053-11 containing Clearify Visualization System (5303907).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0770-2026·2026-08-26

    Sun Pharmaceutical Recalls Carbamazepine Tablets Due to Manufacturing Deviations

    Sun Pharmaceutical Industries is recalling 1,968 bottles of Carbamazepine 200mg tablets due to CGMP deviations and black spots found on tablets.

    Product
    Carbamazepine Tablets, USP, 200mg, 1000 count bottles, Rx only, Manufactured by: Taro Pharmaceutical Industries Ltd., Haifa Bay, Israel 2624761, Distributed by: Taro Pharmaceuticals USA, Inc., Hawthorne, NY 10532, NDC 51672-4005-3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2986-2026·2026-08-26

    ConvaTec Esteem Body Soft Convex Urostomy Pouches Recalled for Leakage

    ConvaTec is recalling Esteem Body Soft Convex Urostomy Pouches because they may leak from the cap during use.

    Product
    Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710, 423712, 423713, 423714, 423715, 423716, 423717, 423718, 423721, 423722, 423723, 423725, 423726, 423727.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0765-2026·2026-08-26

    Shilpa Medicare Recalls Discolored PEMRYDI RTU Injection Vials

    Shilpa Medicare is recalling 9,489 vials of PEMRYDI RTU (pemetrexed disodium) due to reports of green to dark green discoloration in the solution.

    Product
    PEMRYDI RTU — PEMRYDI RTU (PEMETREXED DISODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2951-2026·2026-08-26

    Foundation Medicine Recalls Hamilton Microlab STAR Liquid Handler Software

    Foundation Medicine is recalling 32 Hamilton Microlab STAR Liquid Handler units due to a software issue causing spontaneous closures.

    Product
    Hamilton Microlab STAR Liquid Handler; Protocol Configuration Tool (PCT) v2.0.0. Used to conduct F1CDx and F1LCDx.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2971-2026·2026-08-26

    Paragon 28 Recalls Custom Foot Implant Due to Material Defect

    Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.

    Product
    Custom Made Device Implant 6123 Navicular Cage Small Right Rev A, Model/Catalog Number 6123S R; foot implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2968-2026·2026-08-26

    Gentherm Medical Recalls Blanketrol II Thermal Regulating Systems

    Gentherm Medical is recalling 182 Blanketrol II Model 222S thermal regulating systems because overheating of the 115V CPU board may cause the device to shut down.

    Product
    Blanketrol II Model 222S; Thermal regulating system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1234-2026·2026-08-26

    Prospector Popcorn Fudge Brownie Popcorn Recalled for Nutrient Labeling Errors

    Prospector Popcorn is recalling Fudge Brownie Gourmet Popcorn because the packaging incorrectly lists higher amounts of potassium and calcium than the product actually contains.

    Product
    Prospector Popcorn Fudge Brownie Gourmet Popcorn 1.5oz and 3.5oz
    Category
    Food
    Distribution
    45 states
  • ModerateFDA (Devices)·Z-2950-2026·2026-08-26

    EndoFLIP System Recall Due to Incorrect Catheter Expiration Flags

    FDA is recalling 327 EndoFLIP Systems because a software error incorrectly flags catheters as expired, making them unavailable for clinical procedures.

    Product
    EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684 Endoscopic measuring system, including catheter components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0774-2026·2026-08-26

    Mylan Recalls Acamprosate Calcium Tablets Due to Dissolution Failure

    Mylan Pharmaceuticals is recalling Acamprosate Calcium tablets that failed to meet dissolution specifications.

    Product
    ACAMPROSATE CALCIUM — ACAMPROSATE CALCIUM (ACAMPROSATE CALCIUM ENTERIC-COATED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-1235-2026·2026-08-26

    Prospector Popcorn Recalled for Inaccurate Nutrient Labeling

    Prospector Popcorn is recalling Belgian Chocolate Toffee Gourmet Popcorn due to inaccurate nutrient declarations for Iron and Vitamin D.

    Product
    Prospector Popcorn Belgian Chocolate Toffee Gourmet Popcorn 3.5oz
    Category
    Food
    Distribution
    45 states
  • LowFDA (Devices)·Z-2972-2026·2026-08-26

    Paragon 28 Recalls Custom Foot Implant Due to Material Defect

    Paragon 28, Inc. is recalling a custom-made foot implant due to elevated oxygen levels that may reduce material ductility.

    Product
    Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A, Model/Catalog Number 6123N R; foot implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V547000·2026-08-25

    Ford Recalls 2024-2026 Mustangs for Wiring Harness Ground Fracture Risk

    Ford is recalling 2024-2026 Mustangs because engine compartment wiring harness ground connections may fracture, potentially causing loss of drive power or essential vehicle functions.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V548000·2026-08-25

    Ford Recalls 2026 Vehicles for Engine Piston Dome Manufacturing Defect

    Ford is recalling 2026 Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles because incorrectly manufactured engine piston domes may fail, causing a loss of drive power.

    Product
    FORD — FORD MUSTANG, RANGER, BRONCO, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V550000·2026-08-25

    Ford Recalls 2026 Maverick, F-150, and Bronco Sport for Joint Issues

    Ford is recalling 2026 Maverick, F-150, and Bronco Sport vehicles because improperly tightened joints may lead to detached parts or loss of vehicle control.

    Product
    FORD — FORD MAVERICK, F-150, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V549000·2026-08-25

    Mitsubishi Recalls Outlander Models for Rearview Camera Software Defect

    Mitsubishi is recalling 2025-2026 Outlander and 2026 Outlander PHEV vehicles because a software error may prevent the rearview camera image from displaying, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V546000·2026-08-24

    2027 Thomas Built School Buses Recalled for Missing Seat Belt Anchor Plates

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER EFX2 and HDX2 school buses because missing connector plates may compromise seat belt anchorages and body joint strength.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX2, SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E060000·2026-08-24

    Rennline Recalls Lower Control Arms Due to Subframe Damage Risk

    Rennline Automotive is recalling 106 lower control arms that may have incorrect dimensions, potentially damaging the subframe and causing loss of steering control.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V544000·2026-08-21

    PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Seat Heater Fire Risk

    PACCAR is recalling 811 specific 2027 Kenworth and Peterbilt trucks because a missing heat-shrink on the seat ventilation harness may cause a short circuit and fire.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 579, 567, 589
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V542000·2026-08-21

    T.A. Pelsue Recalls 2024-2025 Trailers Due to Axle Bracket Defect

    T.A. Pelsue is recalling 2024-2025 Fost XL, FiberLite, and MPCCT trailers because axle mounting brackets may crack and fail, increasing crash risk.

    Product
    PELSUE — PELSUE MPCCT, FOST XL, FIBERLITE XL TRADESMAN, FIBERLITE POD TRADESMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide