The Recall Desk

State

Louisiana product recalls

72,919 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,922
Critical
1,094
Severe
1,483
Most recent
2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2351–2375 of 79841

  • HighFDA (Drugs)·D-0453-2026·2026-04-22

    HydroPeptide Clear Alliance benzoyl peroxide serum recalled over benzene contamination

    HydroPeptide Clear Alliance Serum, a 2.5% benzoyl peroxide product, is being recalled because of chemical contamination from the presence of benzene. 9,850 bottles are affected.

    Product
    HydroPeptide CLEAR ALLIANCE SERUM, 2.5% BENZOYL PEROXIDE, a)1 FL OZ/30ml; b) 2 FL OZ/60ml spray bottle; DIST BY HYDROPEPTIDE LLC, ISSAQUAH, WA 98027
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0449-2026·2026-04-22

    Cipla cinacalcet 30 mg tablets exceed the nitrosamine daily intake limit

    Cipla is recalling Cinacalcet Hydrochloride Tablets, 30 mg, over CGMP deviations and the presence of N-Nitroso Cinacalcet above the acceptable daily intake limit. 113,336 bottles are affected.

    Product
    CINACALCET — CINACALCET (CINACALCET)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1806-2026·2026-04-22

    Yeastone Broth recalled because it may report incorrect susceptibility results

    Yeastone Broth is being recalled because the product may report incorrect antifungal susceptibility results during quality control, which could delay treatment or force a change of agent.

    Product
    Yeastone Broth, 11ML, 10/BOX YY3462
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1819-2026·2026-04-22

    Cytal Burn Matrix recalled over out-of-specification endotoxin test results

    Cytal Burn Matrix 7x10 cm wound dressings are being recalled because of an increased rate of out-of-specification endotoxin results. Seven units are affected.

    Product
    Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0487-2026·2026-04-22

    Skin Script blemish spot treatment recalled for failing stability specifications

    Skin Script Blemish Spot Treatment containing 1% salicylic acid is being recalled after it failed stability specifications. The action covers 28,163 bottles.

    Product
    Blemish Spot Treatment (Salicylic Acid) 1%, .5 fl oz (15 ml) bottles, Skin Script, Chandler, AZ 85226, UPC 6 10563 13873 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1809-2026·2026-04-22

    iLet Ace insulin pump lock screens can be bypassed by users

    iLet Ace Pump Kits are being recalled because active status bar icons on the lock and passcode screens allow those screens to be bypassed, permitting unauthorized access.

    Product
    iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1822-2026·2026-04-22

    Cellex photopheresis kit centrifuge bowls may dislodge and break

    Cellex Photopheresis Kits are being recalled because the centrifuge bowl is harder to install and, if fitted improperly, may dislodge and break during priming or treatment.

    Product
    Brand Name: Cellex Photopheresis System Product Name: CELLEX Photopheresis Kit Model/Catalog Number: CLXUSA Software Version: Not Applicable Product Description: THERAKOS Photopheresis or extracorporeal photopheresis (ECP) is a photoimmune therapy where leukocytes are separa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V259000·2026-04-22

    Trails West RPM Freeride Recalled for Cooktop Flame Fire Risk

    Trails West is recalling 2027 RPM Freeride recreational trailers because the cooktop flame may invert during furnace operation, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST RPM FREERIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0532-2026·2026-04-22

    Huons lidocaine 2% injection recalled over lack of sterility assurance

    Lidocaine HCl Injection, USP 2% in 5 mL single-dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0529-2026·2026-04-22

    Huons lidocaine injection recalled nationwide over lack of sterility assurance

    Lidocaine HCl Injection, USP 1% in 5 mL single dose vials manufactured by Huons is being recalled for lack of assurance of sterility. All lots within expiry are affected.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1812-2026·2026-04-22

    Instinct Plus endoscopic clipping devices may malfunction during use

    The Instinct Plus Endoscopic Clipping Device is being recalled after increased complaints indicating the device has the potential to malfunction. 713,702 units are affected.

    Product
    Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0531-2026·2026-04-22

    Spectra sodium chloride ampules recalled over lack of sterility assurance

    0.9% Sodium Chloride Injection, USP in 10 mL single dose ampules supplied for Spectra Medical Devices is being recalled for lack of assurance of sterility. 7,120,750 ampules are affected.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0465-2026·2026-04-22

    Quality Choice cherry cough drops recalled after facility inspection findings

    QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, cherry flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS HONEY LEMON SUGAR FREE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0462-2026·2026-04-22

    MGC Health 30-count honey lemon cough drops recalled after inspection findings

    MGC Health Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    MGC HEALTH — MGC HEALTH (COUGH DROPS HONEY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0477-2026·2026-04-22

    Taro fluocinonide cream 60 g tubes fail viscosity stability specifications

    Taro is recalling one lot of Fluocinonide 0.05% Cream in 60 g tubes after stability testing returned viscosity results above the specification limit. 2,640 tubes are affected.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0482-2026·2026-04-22

    Rhonda Allison calming skin gel recalled as a subpotent hydrocortisone product

    Essential Calming Skin Gel containing 1% hydrocortisone is being recalled because the product is subpotent. The action covers 299 bottles.

    Product
    Essential Calming Skin Gel, hydrocortisone 1%, 120mL/4oz net wt. (113g) per jar, Distributed By: A.C.E. Inc., DFW Intl. Airport, Texas 75261, www.RHONDAALLISON.COM, NDC 66915-531-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0510-2026·2026-04-22

    Apotek desmopressin nasal spray recalled over dislodged or missing cap liners

    Apotek is recalling one lot of Desmopressin Nasal Spray, USP because of a defect in a batch of bottle caps involving dislodged or missing cap liners.

    Product
    DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0469-2026·2026-04-22

    Quality Choice menthol cough drops recalled after facility inspection findings

    QC Quality Choice Menthol Cough Suppressant Oral Anesthetic Cough Drops, menthol flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE — QUALITY CHOICE (COUGH DROPS MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0457-2026·2026-04-22

    Menthol Flavor Cough Drops Recalled Due to Potential Product Quality Issues

    Xiamen Kang Zhongyuan Biotechnology Co., Ltd. is recalling Menthol Flavor Cough Drops due to quality concerns identified during an FDA inspection.

    Product
    MENTHOL FLAVOR COUGH DROP — MENTHOL FLAVOR COUGH DROP (MENTHOL FLAVOR COUGH DROP)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0467-2026·2026-04-22

    Quality Choice strawberry throat drops recalled after facility inspection findings

    QC Quality Choice Pectin Oral Demulcent Throat Soothing Drops, creamy strawberry flavour, 30-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY — QUALITY CHOICE COUGH DROPS CREAMY STRAWBERRY (COUGH DROPS CREAMY STRAWBERRY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0463-2026·2026-04-22

    MGC Health 80-count honey lemon cough drops recalled after inspection findings

    MGC Health Menthol Cough Suppressant Oral Anesthetic Cough Drops, honey lemon, 80-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    MGC HEALTH — MGC HEALTH (COUGH DROPS HONEY)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0458-2026·2026-04-22

    Caring Mill cherry cough drops recalled after facility inspection findings

    Caring Mill Menthol Cough Suppressant Oral Anesthetic Cough Drops, cherry, 90-count bags, are being recalled following FDA observations at the manufacturing facility.

    Product
    CARING MILL COUGH DROPS CHERRY — CARING MILL COUGH DROPS CHERRY (MENTHOL)
    Category
    Drug
    Distribution
    Distributed nationwide