The Recall Desk

State

Florida product recalls

73,388 recalls have nationwide distribution and so reach Florida. 12,858 additional recalls listed Florida specifically in their distribution scope.

What the numbers show

Total
12,858
Critical
1,775
Severe
3,453
Most recent
2026-10-07

Of the 12,858 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 3,453 (27%) are Severe.

These figures cover only the 12,858 recalls whose distribution notice names Florida specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20701–20725 of 86246

  • HighFDA (Devices)·Z-0290-2023·2022-11-30

    Eye Surgery Convenience Kits Recalled for Containing Recalled 3M Drapes

    ROi CPS LLC recalled 76 regard Vitrectomy Pack surgical kits distributed in Louisiana, Missouri, North Carolina, and Florida because they contained 3M surgical drapes that were subsequently recalled.

    Product
    regard VITRECTOMY PACK, EY00266H, Item Number 800028008; eye surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0285-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included Recalled Surgical Drapes

    ROi CPS LLC is recalling 326 regard TOTAL JOINT surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida. The kits contain 3M surgical drapes that were previously recalled. No illnesses or injuries have been reported.

    Product
    regard TOTAL JOINT, OR00446F, Item Number 880291; orthopedic surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0267-2023·2022-11-30

    Ventilator Screen Backlight Malfunction Causes Temporary Display Loss

    Hamilton-C6 ventilators are subject to a backlight malfunction causing the display screen to go black for 2-3 seconds. The FDA has classified this Class II recall as affecting 443 U.S. systems distributed nationwide.

    Product
    Hamilton-C6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-11302022-01·2022-11-30

    USDA Issues Public Health Alert for Summer Sausage Due to Plastic Contamination

    USDA issued a public health alert for fully cooked summer sausage products from Paradise Locker Meats due to possible plastic contamination. No illnesses have been reported.

    Product
    Paradise Locker Meats — FSIS Issues Public Health Alert for Fully Cooked Summer Sausage Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0322-2023·2022-11-30

    Shoulder arthroscopy surgical convenience kits recalled due to defective 3M drapes

    ROi CPS LLC is recalling 90 regard shoulder arthroscopy surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled. The kits were distributed in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard SHOULDER ARTHROSCOPY, OR01103A, Item Number 880471001; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0278-2023·2022-11-30

    PAJUNK Continuous Epidural Tray Recalled for Wrong Medication in Kit

    Pajunk Medical Systems is recalling PAJUNK Continuous Epidural Trays (Model TAL101, Lot 0001359) because some contain 0.75% Marcaine Spinal instead of the intended 0.9% Sodium Chloride. This medication substitution could lead to improper drug administration during epidural procedures.

    Product
    PAJUNK Continuous Epidural Tray, Tuohy Epidural Needle 17G x 4" with EpiLong Soft Catheter, Closed Tip, 19G, Model #TAL101, sterile, each tray contains 5ml Ampule 1% Lidocaine HCl, 10ml Ampule 0.9% Sodium Chloride, and 5ml Ampule 1.5% Lidocaine HCl with Epinephrine 1:200,000.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0282-2023·2022-11-30

    VS3 Iridium Visionsense Beam Combiner Optical Fiber Cable Damage Risk

    Visionsense VS3 Iridium beam combiners may develop damaged optical fiber cables through handling or bending, causing loss of functionality and potential cable heating or melting. Affected units were distributed nationwide in the US.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Light Integrator (Beam Combiner) Product Number: 161-0001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0283-2023·2022-11-30

    Regard LAMINECTOMY surgical kits recalled due to recalled 3M drapes

    ROi CPS LLC is recalling Regard LAMINECTOMY surgical convenience kits because they contain 3M surgical drapes that were subsequently recalled.

    Product
    regard LAMINECTOMY, NU01140, Item Number 900940; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-0166-2023·2022-11-30

    G FUEL Watermelon Limeade Energy Drink recalled for incorrect caffeine labeling

    G FUEL LLC is recalling 48,000 units of GFUEL brand Watermelon Limeade Energy Drink nationwide because the product label does not declare the correct amount of caffeine.

    Product
    GFUEL brand Watermelon Limeade Energy Drink; 16 fl. oz.; ready-to-drink energy beverage in a can
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0311-2023·2022-11-30

    Neuro surgery kits recalled for defective 3M surgical drapes

    ROi CPS LLC is recalling 790 neuro surgery convenience kits that contained 3M surgical drapes which were subsequently recalled. The kits were distributed to Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard MINOR NEURO, NU00140AD, Item Number 880135030; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0294-2023·2022-11-30

    Surgical Convenience Kits Recalled for Containing Recalled 3M Surgical Drapes

    ROi CPS LLC is recalling 170 surgical convenience kits containing 3M surgical drapes that were previously recalled. The kits were distributed to medical facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard SHOULDER W BCH CHAIR, OR00356F, Item Number 800203006; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0293-2023·2022-11-30

    Surgical convenience kits recalled due to defective surgical drapes

    Regard MAJOR EAR surgical convenience kits distributed in Louisiana, Missouri, North Carolina, and Florida are being recalled because the kits contained 3M surgical drapes that were subsequently recalled.

    Product
    regard MAJOR EAR, ET00326J, Item Number 800070010; ear surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0301-2023·2022-11-30

    Surgical kits recalled: Regard VITRECTOMY PK contained 3M recalled components

    Regard VITRECTOMY PK surgical convenience kits are being recalled because they contain 3M surgical drapes that were separately recalled. Affected kits were distributed in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard VITRECTOMY PK, EY00938C, Item Number 800733003; EYE surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0274-2023·2022-11-30

    Basin Set Medical Device Kit Contents Do Not Match Label

    American Contract Systems, Inc. is recalling a surgical basin set (MEBS42K) because the kit contents do not match the labeled contents. The mismatch could result in improper surgical preparation.

    Product
    BASIN SET, MEBS42K, general surgical kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0168-2023·2022-11-30

    Tomato Head Black Bean Sriracha Hummus Recalled for Potential Metal Fragments

    Tomato Head Foods is recalling Tomato Head Black Bean Sriracha Hummus packaged in 8oz cups due to potential metal fragments in the product.

    Product
    The Tomato Head Black Bean Sriracha Hummus packaged in 8oz PPE plastic cups - 8 cups per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0319-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Included 3M Surgical Drapes

    ROi CPS LLC is recalling 54 regard LATERAL SHOULDER surgical convenience kits containing 3M surgical drapes that were subsequently recalled by the manufacturer. Affected kits were distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard LATERAL SHOULDER, OR01044C, Item Number 880435003; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0321-2023·2022-11-30

    Regard SPINE Surgical Kits Recalled for Containing Unsafe Drapes

    ROi CPS LLC is recalling 302 Regard SPINE surgical convenience kits containing 3M surgical drapes that were subject to an FDA recall. Affected kits were distributed in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard SPINE, OR01100A, Item Number 880468001; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0312-2023·2022-11-30

    Neurosurgery convenience kits recalled due to included recalled surgical drapes

    ROi CPS LLC is recalling 248 regard NEURO TRAY neurosurgery convenience kits because they contain 3M surgical drapes that were previously recalled. The kits were distributed in LA, MO, NC, and FL.

    Product
    regard NEURO TRAY, NU00160R, Item Number 880158018; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0300-2023·2022-11-30

    Regard Retinal Pack surgical kits recalled for defective 3M drapes

    ROi CPS LLC is recalling Regard Retinal Pack surgical kits distributed in Louisiana, Missouri, North Carolina, and Florida because they contained recalled 3M surgical drapes.

    Product
    regard RETINAL PACK, EY00935C, Item Number 800730003; EYE surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0304-2023·2022-11-30

    Hip Arthroplasty Surgical Convenience Kits Recalled Due to Defective 3M Drapes

    ROi CPS LLC is recalling regard TOTAL HIP ARTHROPLASTY surgical convenience kits containing recalled 3M surgical drapes distributed to facilities in Louisiana, Missouri, North Carolina, and Florida.

    Product
    regard TOTAL HIP ARTHROPLASTY A&B, OR00032W, Item Number 880028023; ortho surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0292-2023·2022-11-30

    Neurosurgery Kits Recalled Due to Defective 3M Surgical Drapes

    ROi CPS LLC is recalling 38 neurosurgery convenience kits distributed in four states because they contain 3M surgical drapes that were separately recalled.

    Product
    regard CERVICAL PACK, NU00303H, Item Number 800058008; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0280-2023·2022-11-30

    Visionsense Infrared Microscope Recalled Due to Optical Fiber Cable Damage

    Visionsense is recalling 205 units of its VS3 Iridium microscope because optical fiber cables may become damaged during handling, causing loss of function and outer cable heating or melting.

    Product
    VS3 Iridium Visionsense Infrared (IR) Fluorescence Miniature Microscope (MMS-IR) Product Number: 174-0012
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0279-2023·2022-11-30

    Surgical Blade Safety Cartridges Recalled Due to Missing Sterilization

    Southmedic is recalling 450 units of sterile surgical blade cartridges (Lot W92761) because the product was not sterilized but was labeled and distributed as sterile. Non-sterile surgical blades could cause infection if used on patients.

    Product
    Southmedic SAFETY CARTRIDGE WITH SOUTHMEDIC PLUS SURGICAL BLADE, REF 73-8020, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0288-2023·2022-11-30

    Surgical Convenience Kits Recalled Due to Defective 3M Surgical Drapes

    ROi CPS LLC is recalling regard BASIC NEURO surgical convenience kits containing 3M surgical drapes that were previously recalled. Affected units were distributed to LA, MO, NC, and FL.

    Product
    regard BASIC NEURO, NU00259S, Item Number 800021019; neuro surgery convenience kit
    Category
    Medical Device
    Distribution
    4 states