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
1,775
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.

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.

826–850 of 86451

  • ModerateFDA (Devices)·Z-3101-2026·2026-09-09

    Cardinal Health Recalls Presource Packs with Potentially Contaminated Wipes

    Cardinal Health 200, LLC is recalling 1,398 Presource Packs containing CliniClean Pericare Wipes that may be contaminated with a manufacturing lubricant.

    Product
    Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, BLO ROBOTIC GYN , Catalog Number: PBCGRGB28; 2) KIT , GYN MAJOR BARNES JEWIS, Catalog Number: PBVMLP22G; 3) KIT, GYN OPERATIVE LAPAROSCOPY, Catalog Number: PBVM0722D…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0833-2026·2026-09-09

    Supernus Recalls Trokendi XR Topiramate Capsules for Dissolution Failure

    Supernus Pharmaceuticals is recalling Trokendi XR (topiramate) extended-release capsules because they failed dissolution specifications. The recall covers 11,304 bottles distributed nationwide.

    Product
    Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma Solutions, Winchester, KY 40391 USA, Manufactured for: Supernus Pharmaceuticals, Inc., Rockville, MD 20850 USA, NDC 17772-102-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0840-2026·2026-09-09

    Buprenorphine Sublingual Tablets Recalled for Labeling Mix-up

    American Health Packaging is recalling 10,953 cartons of Buprenorphine Sublingual Tablets due to a label mix-up. The affected lot is distributed nationwide.

    Product
    BUPRENORPHINE — BUPRENORPHINE (BUPRENORPHINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3089-2026·2026-09-09

    B Braun Recalls Discofix Stopcock Sets Due to Incorrect Expiration Date

    B Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the carton shipper labels display an incorrect expiration date.

    Product
    Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V575000·2026-09-07

    Can-Am Recalls Motorcycles Due to Instrument Cluster Freezing Risk

    Bombardier Recreational Products is recalling specific Can-Am motorcycles because the touchscreen instrument cluster may freeze or go blank, hiding critical safety information.

    Product
    CAN-AM — CAN-AM SPYDER RT, SPYDER F3, PULSE, ORIGIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-020-2026·2026-09-06

    Imported Pork Guanciale Recalled for Possible Listeria Contamination

    Prime Line Distributors and Ferrarini USA are recalling imported pork guanciale due to possible Listeria monocytogenes contamination found during routine testing.

    Product
    Prime Line Distributors, Inc. and Ferrarini USA, Inc. Recall Imported Ready-To-Eat Pork Guanciale Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    10 states
  • HighNHTSA·26V574000·2026-09-04

    Kibbi Recalls 2026-2027 Renegade RVs Due to Fire Risk

    Kibbi is recalling 2026-2027 Renegade recreational vehicles because a rooftop fan component may overheat and cause a fire.

    Product
    RENEGADE — RENEGADE CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26746·2026-09-03

    Mondraker Recalls Mountain Bicycles with ONOFF S9 Carbon Handlebars

    Mondraker USA is recalling specific mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars because they may crack or fracture, posing a risk of serious injury or death.

    Product
    Mondraker mountain bicycles equipped with ONOFF S9 Carbon MTB handlebars.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V573000·2026-09-03

    Nova Bus Recalls LFS Models Due to Coolant Sensor Defect

    Nova Bus is recalling 2022-2024 LFS and LFS Artic buses because a faulty coolant sensor may cause unexpected engine shutdowns, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26734·2026-09-03

    Amana Through-The-Wall Air Conditioners Recalled Due to Fire Risk

    Daikin Comfort Technologies is recalling Amana Through-The-Wall air conditioners and heat pumps because a shorted component can cause fire and serious injury.

    Product
    Amana Through the Wall (TTW) air conditioners or heat pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26731·2026-09-03

    CPSC Recalls Cambridge Audio Yoyo (M) Bluetooth Speakers Due to Fire Hazard

    Audio Partnership is recalling Cambridge Audio Yoyo (M) Bluetooth speakers because their lithium-ion batteries can overheat and cause fires. No injuries have been reported.

    Product
    Cambridge Audio Yoyo (M) Portable Bluetooth Speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E062000·2026-09-03

    Nova Bus Recalls Casco Engine Coolant Level Sensors

    Nova Bus is recalling Casco engine coolant level sensors that may send false signals, causing unexpected engine shutdowns and increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:COOLING SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26739·2026-09-03

    Skip Hop Recalls Elmo Silicone Teethers Due to Choking Hazard

    Skip Hop is recalling Baby Sesame Street Elmo Silicone Teethers because the black eyes can detach if frozen, posing a choking risk.

    Product
    Baby Sesame Street Elmo Silicone Teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26740·2026-09-03

    Truststone Recalls XO Poppy Magnetic Wireless Power Banks Due to Fire Hazards

    Truststone Group is recalling XO Poppy Power Trip Magnetic Wireless Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn risks.

    Product
    XO Poppy Power Trip Magnetic Wireless Power Banks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26741·2026-09-03

    Clorox Recalls Scented Mistolin and Lestoil Cleaners in Puerto Rico

    Clorox is recalling about 6.3 million bottles of scented Mistolin and Lestoil cleaners sold in Puerto Rico and the U.S. Virgin Islands due to potential bacterial contamination.

    Product
    Scented Mistolin® Dilutable Cleaners and Lestoil® Heavy Duty Multi-Purpose Cleaners sold in Puerto Rico and the U.S. Virgin Islands.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1264-2026·2026-09-02

    Outshine Strawberry Fruit Bars Recalled for Potential Glass Contamination

    Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.

    Product
    Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0803-2026·2026-09-02

    ACTHAR Gel Recalled for Presence of Glass and Stopper Particulate Matter

    Mallinckrodt is recalling ACTHAR Gel vials due to the presence of glass and stopper pieces. Patients should stop using the product and contact their healthcare provider.

    Product
    ACTHAR — ACTHAR (REPOSITORY CORTICOTROPIN)
    Category
    Drug
    Distribution
    Distributed nationwide