The Recall Desk

State

Louisiana product recalls

73,827 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,966
Critical
1,107
Severe
1,740
Most recent
2026-11-04

Of the 6,966 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,740 (25%) are Severe.

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50376–50400 of 80793

  • LowFDA (Devices)·Z-0598-2017·2016-11-23

    Philips IQon Spectral CT System Recalled for Incorrect Label Rating

    Philips Medical Systems is recalling three IQon Spectral CT systems because the product labels do not include the correct current rating.

    Product
    IQon Spectral CT Computed Tomography X-ray system, Model 728332
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-0593-2017·2016-11-23

    Philips Brilliance iCT Computed Tomography System Recalled for Labeling Error

    Philips Medical Systems is recalling 67 Brilliance iCT Computed Tomography X-ray systems because the product labels do not include the correct current rating.

    Product
    Brilliance iCT Computed Tomography X-ray system, Model 728306
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-0596-2017·2016-11-23

    Philips CT Scanner Recall for Incorrect Product Label Rating

    Philips is recalling 15 Ingenuity Core 128 CT scanners because the product labels do not include the correct current rating.

    Product
    Ingenuity Core 128 Computed Tomography X-ray system, Model 728323
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Drugs)·D-0139-2017·2016-11-23

    CutisPharma Recalls Omeprazole Compounding Kits Due to Labeling Error

    CutisPharma is recalling 5,904 kits of FIRST Omeprazole 2mg/mL because the package insert incorrectly lists the strength as 3mg/mL.

    Product
    FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit , 3 OZ, Rx only, Manufactured for CutisPharma Wilmington, MA, NDC# 65628-070-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0142-2017·2016-11-23

    GSK Recalls Zeasorb AF Antifungal Cream Due to Labeling Errors

    GSK Consumer Healthcare is recalling Zeasorb AF antifungal cream because some bottles have incorrect NDC codes or indications on the labels.

    Product
    Zeasorb AF (miconazole nitrate), 2%, cures most athlete's foot, Net wt. 2.5 OZ (71 g), Manufactured for: Steifel Laboratories, Inc., Research Triangle Park, NC 27709, UPC 0 73462 15065 1; NDC 0145-1506-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0401-2017·2016-11-23

    Siemens Recalls Dimension Vista IRON Flex Reagent Cartridges

    Siemens Healthcare Diagnostics is recalling Dimension Vista IRON Flex reagent cartridges due to deferoxamine interference at concentrations not listed in the Instructions for Use.

    Product
    Dimension Vista IRON Flex reagent cartridges
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0138-2017·2016-11-23

    CutisPharma Recalls Omeprazole Kits Due to Labeling Error

    CutisPharma is recalling 8,748 Omeprazole compounding kits because the package insert incorrectly lists the strength as 3mg/mL instead of 2mg/mL.

    Product
    FIRST Omeprazole 2mg/mL in FIRST PPI Suspension Compounding Kit , 5 oz., Rx only, Manufactured for CutisPharma Wilmington, MA, NDC# 65628-070-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0597-2017·2016-11-23

    Philips CT System Recalled for Incorrect Label Rating

    Philips is recalling two Ingenuity Core CT systems because the product labels do not include the correct current rating.

    Product
    Ingenuity Core Computed Tomography X-ray system, Model 728321
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-0594-2017·2016-11-23

    Philips Brilliance CT System Recalled for Incorrect Label Rating

    Philips is recalling three Brilliance ICT SP CT systems because the product labels do not include the correct current rating.

    Product
    Brilliance ICT SP Computed Tomography X-ray system, Model 728311
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-0595-2017·2016-11-23

    Philips Ingenuity CT System Recalled for Incorrect Label Rating

    Philips is recalling 27 Ingenuity CT systems because the product labels do not include the correct current rating.

    Product
    Ingenuity CT Computed Tomography X-ray system, Model 728326
    Category
    Medical Device
    Distribution
    15 states
  • SevereUSDA FSIS·111-2016·2016-11-22

    Heinz Recalls Mislabeled Au Jus Gravy Containing Undeclared Allergens

    H.J. Heinz is recalling approximately 5,022 pounds of bistro au jus gravy that was incorrectly labeled as pork gravy. The product contains undeclared milk and soy allergens.

    Product
    H.J. Heinz Co. Recalls Products Incorrectly Labeled As Pork Gravy Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17714·2016-11-22

    BRP Recalls 2017 Can-Am Maverick X3 Side-by-Side Off-Road Vehicles

    BRP is recalling about 2,380 model year 2017 Can-Am Maverick X3 side-by-side off-road vehicles because a steering defect can cause loss of control and crashes.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V846000·2016-11-22

    Forest River Recalls 2017 XLR Trailers for Incorrect Federal Placard

    Forest River is recalling certain 2017 XLR Toyhauler trailers because they may have an incorrect Federal Placard that fails to indicate a third axle.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V847000·2016-11-22

    Nissan Recalls 2016 Titan XD Trucks for Fuel Tank Ventilation Defect

    Nissan is recalling 12,112 model year 2016 Titan XD diesel vehicles because a fuel tank breather tube may not be properly connected, causing inaccurate fuel gauge readings.

    Product
    NISSAN — NISSAN TITAN XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V840000·2016-11-21

    Maserati Recalls Ghibli and Quattroporte Vehicles for Tire Sidewall Cracks

    Maserati is recalling 1,861 Ghibli and Quattroporte vehicles because certain Pirelli tires may develop sidewall cracks, potentially causing air loss and vehicle control issues.

    Product
    MASERATI — MASERATI GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V844000·2016-11-21

    GM Recalls 2016 Buick Cascada for Power Window Safety Standard Violation

    General Motors is recalling 2016 Buick Cascada vehicles because an incorrect roof control module may allow windows to close automatically or remotely, increasing injury risk.

    Product
    BUICK — BUICK CASCADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V842000·2016-11-21

    Hyundai Recalls Tucson and Santa Fe for Trailer Hitch Wiring Defect

    Hyundai is recalling 2016-2017 Tucson and 2017 Santa Fe vehicles because a trailer hitch wiring malfunction may cause brake lights to stay on, confusing other drivers.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V843000·2016-11-21

    Hyundai Recalls 2007-2008 Entourage Vehicles for Hood Latch Defect

    Hyundai is recalling 2007-2008 Entourage vehicles because the secondary hood latch may corrode and fail to engage, increasing crash risk if the hood opens while driving.

    Product
    HYUNDAI — HYUNDAI ENTOURAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V836000·2016-11-18

    Volvo Bus Recalls 9700 Models Due to Engine Stall Risk

    Volvo Bus is recalling 2008-2017 9700 buses because an undersized power feed relay may fail, causing the engine to stall and increasing crash risk.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V838000·2016-11-18

    Navistar Recalls IC Bus CE and BE Models for Heater Hose Defect

    Navistar is recalling 157 IC Bus CE and BE transit buses because a heater hose may split, leaking hot coolant into the driver's foot area.

    Product
    IC BUS — IC BUS CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V839000·2016-11-18

    Maserati Recalls 2017 Models for Backup Camera Software Defect

    Maserati is recalling 7,481 model year 2017 Quattroporte, Ghibli, and Levante vehicles because the backup camera may disable in freezing temperatures, increasing crash risk.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide