The Recall Desk

State

Louisiana product recalls

73,100 recalls have nationwide distribution and so reach Louisiana. 6,958 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,958
Critical
1,109
Severe
1,497
Most recent
2026-09-23

Of the 6,958 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,497 (22%) are Severe.

These figures cover only the 6,958 recalls whose distribution notice names Louisiana specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10876–10900 of 80058

  • HighFDA (Food)·F-1567-2024·2024-08-07

    Vanilla Nut Sundae Cones Recalled for Possible Listeria Contamination

    Yelloh! Classic Vanilla Nut Sundae Cones are recalled nationwide due to possible contamination with Listeria monocytogenes. Consumers should dispose of or return affected packages.

    Product
    Yelloh! Classic Vanilla Nut Sundae Cones 4 fl oz UPC 810038684895. 24 cones wrapped in paper, packaged in cardboard box, 8 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1572-2024·2024-08-07

    Amafruit Superfruits Recalled for Possible Listeria Contamination Nationwide

    Totally Cool, Inc. is recalling Amafruit Superfruits from the Amazon Dragon Fruit due to possible Listeria monocytogenes contamination. The product has been distributed nationwide; consumers should discard or return affected lots.

    Product
    Amafruit Superfruits from the Amazon Dragon Fruit. Packaged in 3 gallon plastic tubs, UPC 855738002242.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1598-2024·2024-08-07

    Marco Green Tea White Chocolate Ice Cream Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Marco Green Tea White Chocolate Ice Cream due to possible contamination with Listeria monocytogenes. The recall affects approximately 10,587 cases distributed nationwide with best-by dates from 06/07/24 to 12/11/25.

    Product
    Marco Green Tea White Chocolate Ice Cream 16 fl oz/1 pint, UPC 860006880521. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2457-2024·2024-08-07

    Arctic Sun Temperature Management System software failure may disable critical safety alarms

    Arctic Sun Temperature Management Systems may fail to reach target temperature and critically fail to alert clinicians. The software defect affects approximately 10,507 units worldwide and risks hypothermia or hyperthermia.

    Product
    Arctic Sun Temperature Management Systems, Name/REF: Arctic Sun STAT, NA/6000-00-00; Arctic Sun STAT Loaner, NA/6000-00-00L; Arctic Sun Stat EU UK/600001; Arctic Sun Stat Taiwan/600006; Arctic Sun Stat Japan/600020; Arctic Sun 5000, NA/5000-00-00; Arctic Sun 5000, NA w/ T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2452-2024·2024-08-07

    Boston Scientific Capio SLIM Device May Fail During Surgical Procedures

    Some lots of the Capio SLIM suture capturing device may fail to consistently catch sutures during surgery, potentially requiring extended procedures or additional medical intervention.

    Product
    Capio SLIM Suture Capturing Device, 1-Pack, UPN: M0068318250. Capio SLIM Suture Capturing Devices are used by physicians to facilitate the consistent placement of sutures during open surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2456-2024·2024-08-07

    Blood Culture Identification Panel May Produce False Positive Results

    The BIOFIRE BCID2 Panel may produce false positive Serratia marcescens results when used with certain culture media bottles, potentially leading to inappropriate changes in patient therapy.

    Product
    BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, for FILMARRAY Systems, when used in conjunction with Culture Media Bottles: BACT/ALERT FA PLUS, REF: 410851, and BACT/ALERT PF PLUS, REF: 410853
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0624-2024·2024-08-07

    Progesterone Injection Recalled for Glass Particulate Matter in Vials

    Eugia US LLC is recalling Progesterone Injection vials nationwide due to glass particles found in the product. Patients and healthcare providers should stop using the affected lot.

    Product
    PROGESTERONE — PROGESTERONE (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1596-2024·2024-08-07

    Marco Vanilla Chai Ice Cream recalled for possible Listeria contamination

    Marco Vanilla Chai Ice Cream 16 fl oz is being recalled due to possible contamination with Listeria monocytogenes. The affected products have best-by dates between 06/07/24 and 12/11/25.

    Product
    Marco Vanilla Chai Ice Cream 16 fl oz/1 pint, UPC 86000199286. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1612-2024·2024-08-07

    Frozen Ice Cream Recalled for Possible Listeria Contamination

    Totally Cool, Inc. recalls Abilyn's Frozen Bakery Cookie Dough Ice Cream due to possible contamination with Listeria monocytogenes. Consumers should not consume affected products.

    Product
    Abilyn's Frozen Bakery Cookie Dough Ice Cream UPC 851545008071. Packaged in cardboard box, 4 boxes per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1556-2024·2024-08-07

    Cumberland Farms Ice Cream Sandwich Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Cumberland Farms Farmhouse Premium Ice Cream Sandwich in Marvelous Mint flavor due to possible Listeria monocytogenes contamination. Approximately 2,409 cases were distributed nationwide.

    Product
    Cumberland Farms Farmhouse Premium Ice Cream Sandwich, Marvelous Mint, 4 fl oz UPC 42704010046. Individually wrapped in plastic, 24 units per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1605-2024·2024-08-07

    Dolcezza Mascarpone & Berries Gelato Recalled for Possible Listeria Contamination

    Totally Cool, Inc. is recalling Dolcezza Mascarpone & Berries Gelato nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Dolcezza Mascarpone & Berries Gelato 16 fl oz/1 pint, UPC 857838006083. Packaged in paper containers, 8 containers per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V584000·2024-08-07

    Genesis GV60 and GV80 Rearview Camera Display May Fail in Reverse

    Hyundai is recalling 2024-2025 Genesis GV60 and 2025 GV80 vehicles because the rearview camera display may shut off when driving in reverse, reducing driver visibility.

    Product
    GENESIS — GENESIS GV60, GV80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V583000·2024-08-07

    2024 Hyundai Sonata Brake Light Software Flaw Increases Crash Risk

    Hyundai is recalling 38,331 2024 Sonata vehicles for a brake light software defect that may cause lights to flash or fail to illuminate. This increases crash risk by confusing other drivers about vehicle movements.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1519-2024·2024-08-07

    NaturesPlus Testosterone Supplement Recalled for Missing Ingredient and Incorrect Formulation

    Natural Organics is recalling NaturesPlus ULTRA T-MALE due to incorrect formulation: the product is missing the ingredient TongKat Ali and contains additional Rhodiola Rosea. No illnesses have been reported.

    Product
    NaturesPlus ULTRA T-MALE Maximum Strength Testosterone Boost for Men 60 Bi-layer Tablets
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2454-2024·2024-08-07

    SOFT-VU KUMPE Catheters Recalled for Mislabeled Inner Pouch

    Angiodynamics is recalling SOFT-VU KUMPE 5F X 65CM angiographic catheters (595 boxes nationwide) because inner pouch labels may show information for a different catheter model while shelf-box labels are correct.

    Product
    SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0623-2024·2024-08-07

    Ciprofloxacin Ophthalmic Solution Recalled Due to Defective Container

    FDC Limited is recalling 66,528 bottles of Ciprofloxacin ophthalmic solution USP 0.3% due to a manufacturing defect in the container cap that prevents access to the medication. All affected bottles were distributed nationwide.

    Product
    CIPROFLOXACIN — CIPROFLOXACIN (CIPROFLOXACIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1520-2024·2024-08-07

    NaturesPlus T-MALE Testosterone Support Supplement Recalled for Ingredient Mismatch

    NaturesPlus T-MALE liquid supplement is being recalled because the product is missing the key ingredient TongKat Ali and contains an additional ingredient, Rhodiola Rosea, that should not be present.

    Product
    NaturesPlus T-MALE Liquid Testosterone Support for Men 8 OZ Berry and 30 OZ Berry
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2453-2024·2024-08-07

    SOFT-VU KUMPE Diagnostic Catheter Recalled for Mislabeled Inner Pouch

    Angiodynamics recalls SOFT-VU KUMPE diagnostic catheters because inner pouch labels may show incorrect catheter length information, while the outer box label is accurate. 519 boxes distributed nationwide.

    Product
    SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0621-2024·2024-08-07

    Prescription azelaic acid gel recalled for manufacturing process deviations

    Glenmark Pharmaceuticals recalls azelaic acid gel 15% nationwide due to manufacturing process deviations. Patients should consult their healthcare provider about their prescription.

    Product
    AZELAIC ACID — AZELAIC ACID (AZELAIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E065000·2024-08-05

    Mack Trucks Recalls Replacement Tie Rods With Defective Ball Studs

    Mack Trucks is recalling certain replacement tie rods equipped with USK ball studs that may break due to incorrect heat treatment, potentially causing loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E064000·2024-08-05

    Volvo Trucks Recalls Replacement Tie Rods Due to Heat-Treatment Defect

    Volvo Trucks is recalling certain replacement tie rods equipped with USK ball studs that may break due to incorrect heat treatment, potentially causing loss of steering control.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide