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.

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.

401–425 of 86443

  • SevereCPSC·27007·2026-10-01

    Designs Direct Recalls Three-Light Floor Lamps Due to Fire and Burn Hazards

    Designs Direct is recalling Cupcakes and Cashmere brand floor lamps because the cord or wiring can overheat, posing fire and burn risks. Consumers should stop using the lamps and request a refund.

    Product
    Designs Direct Cupcakes and Cashmere Brand Three-Light Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V632000·2026-10-01

    2027 Thomas Built Buses Recall for Headlight Software Error

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER C2 and Jouley school buses because a software error may cause low beam headlights to illuminate improperly.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·27009·2026-10-01

    Gobi Heat Recalls Rechargeable Hand Warmers Due to Fire and Burn Hazards

    Gobi Heat is recalling rechargeable hand warmers because the lithium-ion batteries can overheat and ignite, posing a risk of serious injury from fire and burns.

    Product
    Gobi Heat Rechargeable Hand Warmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27012·2026-10-01

    Dollar Tree Recalls Electric Balloon Pumps Due to Burn Hazard

    Dollar Tree is recalling electric balloon pumps that can overheat, posing a burn hazard. Consumers should stop using the pumps and return them for a refund.

    Product
    Electric Balloon Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27010·2026-10-01

    Walmart Recalls Over 4.4 Million Metal Wire Bristle Grill Brushes

    Walmart is recalling over 4.4 million Expert Grill metal wire bristle grill brushes because detached bristles can stick to food, posing an ingestion hazard.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-3194-2026·2026-09-30

    AVID Medical Recalls Halyard IV Start Kits Due to Mold Contamination

    AVID Medical is recalling Halyard IV Start Kits because they contain applicators potentially contaminated with Aspergillus penicillioides.

    Product
    Halyard IV START KIT NON-STERILE; 48 kits per case. Containing BD ChloraPrep Clear - 1 mL Applicator. Kit Model Number: KRIV26-02.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1396-2026·2026-09-30

    Bettergoods Lemon Alfredo Fettuccine Recalled for Listeria Contamination

    GIAS FOOD INC. is recalling Bettergoods Lemon Alfredo Fettuccine due to Listeria monocytogenes contamination. Consumers should stop eating the product and return it to Walmart.

    Product
    Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 20 2027 L6080C, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0862-2026·2026-09-30

    Sterling Recalls Carboxymethylcellulose Sodium Eye Drops Due to Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling specific lots of Cameron Pharmaceuticals Carboxymethylcellulose Sodium 0.5% Eye Lubricant due to a lack of assurance of sterility.

    Product
    Lubricant Eye Drops-Cameron Pharmaceuticals, Carboxymethylcellulose Sodium 0.5%, Eye Lubricant, 0.5 FL OZ (15 mL) bottles, Distributed by Cameron Pharmaceuticals, LLC, Louisville, KY, 40245, NDC 42494-448-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3139-2026·2026-09-30

    CooperSurgical Recalls Infant Nasal CPAP Tubing Due to Loose Connection Risk

    CooperSurgical is recalling specific lots of INCA Infant Nasal CPAP tubing because a loose connection may cause loss of pressure and reduced oxygenation.

    Product
    INCA (Infant Nasal Cannulae Assy) Infant Nasal CPAP, Complete Set. Stay-Flex tubing component. 5 units per box. Model Numbers: 44-2707, 44-2709, 44-2710, 44-2712, 44-2715.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0858-2026·2026-09-30

    Walgreens Lubricant Eye Drops Recalled for Sterility Assurance Concerns

    Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. The recall affects 199,600 packs distributed nationwide.

    Product
    WALGREENS LUBRICANT EYE DROPS — WALGREENS LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V628000·2026-09-30

    Grech Motorhomes Recalled for Rooftop Fan Fire Risk

    Grech is recalling 2026-2027 Strada, Terreno, and Turismo motorhomes because a rooftop ventilation fan circuit board may overheat and cause a fire.

    Product
    GRECH — GRECH TURISMO, STRADA, TERRENO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V627000·2026-09-30

    Highland Ridge Range Lite Air Travel Trailer Fresh Water Tank Recall

    Highland Ridge RV is recalling 2022-2024 Range Lite Air travel trailers because fastener failure may cause the fresh water tank to detach, creating a road hazard.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT RANGE LITE AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0856-2026·2026-09-30

    Sodium Chloride Ophthalmic Solution Recalled for Sterility Assurance Issues

    Sterling Pharmaceutical Services is recalling Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, due to a lack of assurance of sterility.

    Product
    SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% — SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5% (SODIUM CHLORIDE HYPERTONICITY OPHTHALMIC SOLUTION, 5%)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0859-2026·2026-09-30

    Sterling Pharmaceutical Recalls Lubricating Tears Due to Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling specific lots of Lubricating Tears because the company cannot guarantee the product is sterile.

    Product
    LUBRICATING TEARS — LUBRICATING TEARS (CARBOXYMETHYLCELLULOSE SODIUM 0.5% SOLUTION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0860-2026·2026-09-30

    Gentle Eyes Lubricant Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling Gentle Eyes Lubricant Eye Drops due to a lack of assurance of sterility.

    Product
    GENTLE EYES LUBRICANT EYE DROPS — GENTLE EYES LUBRICANT EYE DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0861-2026·2026-09-30

    Sterling Recalls Major LubriFresh P.M. Ointment for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.

    Product
    Major LubriFresh P.M. Nighttime Ointment, Net wt. 0.125 oz. (3.5 g) tubes, Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152, NDC 0904-6488-38
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0863-2026·2026-09-30

    AvKare Carboxymethylcellulose Sodium Eye Drops Recalled for Sterility Concerns

    Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.

    Product
    CARBOXYMETHYLCELLULOSE SODIUM — CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3266-2026·2026-09-30

    Medline Neurological Sponges Recalled for Potential Endotoxin Variability

    Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.

    Product
    Medline Convenience Kits: 1) MAJOR PACK, Catalog Number: DYNJ81325A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3244-2026·2026-09-30

    Olympus BiCOAG Hemostasis Probe Recall Due to Ceramic Tip Detachment Risk

    Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.

    Product
    Olympus BiCOAG Hemostasis Probe 10Fr Coaxial Connector. Model/Catalog Number: CD-B610LA.
    Category
    Medical Device
    Distribution
    Distributed nationwide