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.

10651–10675 of 80058

  • HighFDA (Devices)·Z-2617-2024·2024-08-21

    Spinal Cord Stimulation Devices May Reset During Charging, Causing Transient Therapy Loss

    Boston Scientific spinal cord stimulation implants may reset during routine charging, causing brief loss of therapy. Patients may experience undesired sensations when stimulation restarts, potentially leading to surgical intervention requests.

    Product
    WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2571-2024·2024-08-21

    Merit Medical Convenience Kits with Recalled Syringes Pose Leak Risk

    Merit Medical is recalling 900 convenience kits containing plastic syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: SafeSheath CSG (Introducer Catheter), REF: FCL-069-00/A FCL-069-02/A FCL-069-03/A For the introduction of various types of pacing or defibrillator leads and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0632-2024·2024-08-21

    Ophthalmic solution recalled for defective container with lodged spike

    FDC Limited recalls Timolol Maleate eye drops (362,544 bottles) nationwide due to a manufacturing defect: a yellow spike from the cap lodged in the nozzle, posing a risk of eye injury.

    Product
    TIMOLOL MALEATE — TIMOLOL MALEATE (TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2564-2024·2024-08-21

    FDA recalls Merit Medical convenience kits due to defective syringes

    Merit Medical convenience kits containing plastic syringes are recalled due to identified leaks, breakage, and quality issues that may pose a risk to patient health. The affected kits are used for vascular and cardiac procedures.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: K09/K09T (Custom Manifold Kit), REF: K09-00526L K09-00807AH K09-01467AD K09-01467AF K09-01514U K09-01734L K09-02040C K09-02683F K09-02804B K09-03844F K0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2620-2024·2024-08-21

    Surgical light heads may detach due to weld defects

    DKK Dai-Ichi Shomei is recalling 293 Aurora surgical light heads because the frame welds can crack, potentially causing the light head to detach during use. No injuries have been reported.

    Product
    Aurora 3 Series, Aurora 7 lighthead; Models: AUT7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2618-2024·2024-08-21

    Aurora 7 Surgical Light Heads Recalled for Cracked Weld Frames

    DKK Dai-Ichi Shomei is recalling 555 Aurora 7 surgical light heads because frame welds can crack, causing the frame to sag, the housing to crack, or the light head to detach.

    Product
    Aurora Series, Aurora 7 lighthead; Models: LED7 (including TV models). The Aurora Series is intended to illuminate the surgical field and ensure visibility of the surgical site.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2559-2024·2024-08-21

    Merit Medical catheter extractor kits recalled for syringe quality defects

    Merit Medical is recalling 3,631 catheter extractor convenience kits due to defective syringes with leaks and breakage. The identified quality issues may compromise patient safety during catheter removal.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Outake, REF CET200 and CET300, The Catheter Extractor is a catheter accessory device intended for minimally invasive removal of tunneled long term catheters. T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2579-2024·2024-08-21

    Merit Medical Convenience Kits Recalled for Syringe Leaks and Breakage

    Merit Medical is recalling medical convenience kits with defective syringes due to identified leaks, breakage, and quality issues that may pose a risk to patient health during procedures.

    Product
    Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Customer Procedure Kit (Angiography/Angioplasty kit), REF: K05-02166B K05T-00380C K05T-01674B K05T-01863 K05T-01941C K05T-01955 K05T-02138 K05T-02159 K05T-02272G K05T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2622-2024·2024-08-21

    Salivary Testosterone ELISA Quality Control Failure Invalidates Test Results

    DRG International is recalling Salivary Testosterone ELISA kits (Model SLV-3013) due to out-of-range quality controls that invalidate test runs and delay patient results. The recall affects 257 units distributed nationwide in six states.

    Product
    Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for the quantitative in vitro diagnostic measurement of free active testosterone in saliva.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2580-2024·2024-08-21

    VITROS Folate Reagent Pack Recalled for Delayed Test Results

    Ortho-Clinical Diagnostics is recalling VITROS Folate Reagent Pack due to fibrinogen precipitation causing delayed test results. The recall affects 18,467 units distributed worldwide.

    Product
    VITROS Immunodiagnostic VITROS Folate Reagent Pack 1/2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2545-2024·2024-08-21

    Discrete Chemistry Analyzer Recalled Due to Carousel Malfunction

    Beckman Coulter is recalling 59 units of its Access 2 Immunoassay System Analyzer due to misaligned index wheels causing carousel motion errors that disable the analyzer and cancel patient tests.

    Product
    Discrete photometric chemistry analyzer for clinical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V625000·2024-08-20

    MCI Recalls 2021 D45CRTeLE Buses Due to Battery Fire Risk

    Motor Coach Industries is recalling 2021 D45CRTeLE vehicles because a software error may cause battery damage and increase the risk of fire.

    Product
    MCI — MCI D45CRTELE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24T008000·2024-08-20

    Continental Recalls HDL2 DL+ Tires Due to Belt Separation Risk

    Continental is recalling specific HDL2 DL+ tires because an incorrect rubber compound may cause the steel belt to separate, potentially leading to a loss of vehicle control.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V621000·2024-08-19

    Audi Recalls E-Tron Models Due to Brake Pedal Detachment Risk

    Audi is recalling 2019-2024 E-Tron and E-Tron Sportback vehicles because a faulty fastener may cause the brake pedal to detach, increasing crash risk.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V620000·2024-08-19

    Kalmar Recalls 2016-2017 Ottawa T2 Trucks Due to Brake Defect

    Kalmar is recalling 2016-2017 Ottawa T2 6X4 vehicles because insufficient air tank volume reduces braking performance and increases crash risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V622000·2024-08-19

    Northern Lite Truck Camper Recall for Cooktop Overheating Risk

    Northern Lite is recalling 2022-2024 Truck Campers because a cooktop circuit board may overheat, increasing the risk of a fire.

    Product
    NORTHERN LITE — NORTHERN LITE TRUCK CAMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2024·2024-08-16

    Perdue Recalls Frozen Chicken Nuggets and Tenders Due to Metal Contamination

    Perdue Foods is recalling approximately 167,171 pounds of frozen, ready-to-eat chicken breast nuggets and tenders due to possible metal wire contamination.

    Product
    Perdue Foods LLC — Perdue Foods LLC, Recalls Frozen, Ready-To-Eat Chicken Breast Nugget and Tender Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·24V616000·2024-08-16

    Forest River Recalls 2025 R-POD Travel Trailers Due to Fire Risk

    Forest River is recalling 2025 R-POD RPT203 travel trailers because the exterior griddle may be stowed while connected to the LP gas line, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V618000·2024-08-16

    Winnebago Recalls Travel Trailers Due to Incorrect Electrical Outlet Installation

    Winnebago is recalling certain Minnie, Access, and Voyage travel trailers because a standard outlet may be installed where a GFCI protected outlet is required, increasing the risk of electric shock.

    Product
    WINNEBAGO — WINNEBAGO ACCESS, MINNIE, VOYAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08162024-01·2024-08-16

    USDA Issues Public Health Alert for Illegally Imported Myanmar Meat and Poultry

    USDA FSIS issued a public health alert for meat and poultry products illegally imported from Myanmar, a country ineligible to export to the U.S.

    Product
    FSIS Issues Public Health Alert for Ineligible Meat and Poultry Products Illegally Imported from the Republic of the Union of Myanmar
    Category
    Food
    Distribution
    Distributed nationwide