The Recall Desk

State

Florida product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1026–1050 of 85725

  • SevereCPSC·26599·2026-07-02

    Metalux Optimized High Bay LED Light Fixtures Recalled for Fire Hazard

    Cooper Lighting recalls about 42,000 Metalux Optimized High Bay LED light fixtures due to a fire hazard. The LED board can overheat or contact combustible materials; nine fires have been reported with no injuries or property damage.

    Product
    Metalux Optimized High Bay (OHB) LED Light Fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26595·2026-07-02

    Rowenta Cordless Vacuum Cleaners Recalled for Fire and Burn Hazard

    Rowenta is recalling cordless vacuum cleaners with lithium-ion batteries that can overheat and ignite, posing a risk of fire and burn injury. About 3,660 units are affected; no injuries have been reported.

    Product
    Rowenta Cordless Vacuum Cleaners with lithium-ion battery
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26598·2026-07-02

    Gigglescape Under the Sea Popping Toy Recalled for Choking Hazard

    Target has recalled approximately 49,000 Gigglescape Under the Sea Popping Toys because the clear plastic dome can detach, exposing small plastic balls that pose a choking hazard. One child began to choke after the dome detached.

    Product
    Gigglescape™ Under the Sea Popping Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26592·2026-07-02

    Topyond Pool Drain Ports with Covers Recalled for Entrapment Risk

    Topyond pool drain ports with covers violate federal entrapment protection standards and pose serious injury or death risks from entrapment and drowning. Consumers should stop using pools with these drain ports immediately.

    Product
    Topyond Pool Drain Port with Cover
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26594·2026-07-02

    POPOOO Jungle Safari LED Finger Lights Recalled for Battery Ingestion Risk

    CPSC has recalled POPOOO Jungle Safari LED Finger Lights sold on Amazon because the toys contain easily accessible button cell batteries that can cause serious injury or death if swallowed. No injuries have been reported.

    Product
    POPOOO Jungle Safari LED Finger Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26603·2026-07-02

    Roman Candles 8 Shot Fireworks Recalled for Explosion and Burn Hazards

    Winco Fireworks International is recalling Roman Candles 8 Shot 3-Pack firework devices because the fireworks can malfunction and shots can blow out the side of the tube, posing a risk of serious injury from explosion and burn hazards. No injuries have been reported.

    Product
    Roman Candles 8 Shot 3-Pack Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26596·2026-07-02

    AMASKY Nursing Pillows Recalled for Risk of Suffocation

    AMASKY Nursing Pillows, sold on Amazon from January to March 2026, violate safety standards and can obstruct infant breathing, posing a serious risk of suffocation. No injuries have been reported.

    Product
    AMASKY Nursing Pillows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26E041000·2026-07-02

    Warn Industries Recalls Wireless Remote Kits Due to Winch Movement Risk

    Warn Industries is recalling Wireless Remote Kits (part numbers 90287 and 90289) because the remote control may be incompatible with legacy winches, causing unexpected movement and increasing injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26602·2026-07-02

    Unity 7 Shot 200 Gram Aerial Cake Fireworks Recalled for Explosion and Burn Hazard

    Winco Fireworks International recalls Unity 7 Shot 200 Gram Aerial Cake firework devices that can tip over, creating risk of serious injury from explosion and burns. About 87,120 units sold at Pyro City and independent fireworks stores nationwide from January through May 2026 are affected.

    Product
    Unity 7 Shot 200 Gram Aerial Cake Firework Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1099-2026·2026-07-01

    Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.

    Product
    Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2583-2026·2026-07-01

    Medical Device Surgical Kits with Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes used in surgical procedures. The manufacturer identified unapproved design changes to the products that were not cleared by the FDA through the 510(k) process.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. BARIATRIC DYNJ905153J DYNJ905153K DYNJ905153L GYNE LAPAROTOMY PACK-LF DYNJ49593A LAPAROSCOPY DYNJ905157G DYNJ905157I DYNJ905157J LAPAROSCOPY PACK DYNJ56930B MAJOR PLUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0623-2026·2026-07-01

    ChloraPrep One-Step Topical Solution Sterility Assurance Recall

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) due to wrinkles in the paper lidding that may breach the seal, compromising sterility assurance.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2602-2026·2026-07-01

    Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kit Recall

    Abiomed is recalling Impella CP Set with SmartAssist (10th Generation) containing 14Fr Low Profile Introducer Kits due to potential thrombus (blood clot) formation during prolonged use of the introducer.

    Product
    Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits 13 and 25 cm Japan. Product Code: 1000542.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1112-2026·2026-07-01

    Zapp's Bayou Blackened Ranch Kettle Chips Recalled for Salmonella

    Utz Quality Foods, LLC is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips due to the potential presence of Salmonella. The product was distributed across 32 states.

    Product
    1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2453-2026·2026-07-01

    Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled

    Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2591-2026·2026-07-01

    Medline angiography and radiology convenience kits recalled for unapproved design changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and to Barbados.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO PACK DYNJ30565C DYNJ32555B ANGIO PACK-LF DYNJ0774765U ANGIO TRAY DYNJ46153A ANGIOGRAM TRAY DYNJ33638K ANGIOGRAPHY DRAPE PK QVH-LF DYNJ35110D ANGIOGRAPHY P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1104-2026·2026-07-01

    Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.

    Product
    Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2592-2026·2026-07-01

    Medline Polycarbonate Syringes in Convenience Kits Recalled for Unapproved Design Changes

    Medline Industries recalled multiple convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The company identified these modifications and notified the FDA of the deviation from the approved 510(k) design.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ANGIO DRAPE PACK (ADLUG)642-LF DYNJ47665D ANGIO PACK DYNJ30565D ANGIOGRAPHY PACK-LF DYNJ0854485V ARTERIOGRAM DYNJ28082D DYNJ28082F CARDIAC CATH DYNJ67349 CARDIA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0624-2026·2026-07-01

    ChloraPrep One-Step Topical Antiseptic Recalled for Non-Sterility

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) topical applicators due to non-sterility caused by the presence of Aspergillus penicillioides fungal contamination.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1113-2026·2026-07-01

    Zapp's Brand Bayou Blackened Ranch Potato Chips Recalled for Salmonella

    Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.

    Product
    2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereNHTSA·26V422000·2026-07-01

    BMW Recalls 428 Vehicles for Integrated Brake System Malfunction

    BMW is recalling 428 vehicles from 2023-2025 due to a potential integrated brake system malfunction that may reduce braking power or disable stability controls.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE 740I XDRIVE, 740I, X1, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide