The Recall Desk

State

Louisiana product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43976–44000 of 80775

  • HighNHTSA·18V094000·2018-02-05

    Ferrara Recalls Fire Trucks Due to Corroding Pressure Valve Rings

    Ferrara is recalling specific fire-fighting vehicles because corroding rings may cause pressure relief valves to open, reducing water pressure and hindering fire-fighting efforts.

    Product
    INTERNATIONAL — INTERNATIONAL, KENWORTH, FERRARA 4400, T370, INFERNO, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V090000·2018-02-02

    Jaguar Recalls 2018 Models for Fuel Rail Leak Fire Risk

    Jaguar is recalling 2018 XE, XF, E-PACE, F-PACE, and F-TYPE vehicles because fuel rail end caps may leak, increasing the risk of a fire.

    Product
    JAGUAR — JAGUAR XF, E-PACE, F-TYPE, F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V092000·2018-02-02

    PACCAR Recalls 2017-2018 Kenworth and Peterbilt Trucks for Display Error

    PACCAR is recalling 2017-2018 Kenworth and Peterbilt trucks because the transmission gear display may show incorrectly, potentially preventing the truck from moving.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, 567, T680, T880
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V093000·2018-02-02

    Triple E Recreational Vehicles Recall Fire Extinguishers Due to Clogging Risk

    Triple E is recalling 2002-2013 recreational vehicles because Kidde fire extinguishers may clog or detach, potentially failing to discharge during a fire.

    Product
    TRIPLE E RV — TRIPLE E RV, TRIPLE E EMBASSY, REGAL, EMPRESS, MOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V087000·2018-02-01

    Land Rover Recalls 2018 Models for Fuel Rail Leak Fire Risk

    Jaguar Land Rover is recalling 2018 Discovery Sport, Range Rover Evoque, and Velar vehicles because fuel rail end caps may leak, increasing the risk of a fire.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT, RANGE ROVER EVOQUE, RANGE ROVER VELAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V088000·2018-02-01

    Land Rover Recalls 2018 Range Rover Evoque Convertibles for TPMS Defect

    Jaguar Land Rover is recalling 2018 Range Rover Evoque convertibles with 20-inch wheels because the tire pressure monitoring system may fail to warn drivers of low pressure.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18719·2018-02-01

    John Deere Recalls ZTrak Riding Mowers Due to Laceration Hazard

    John Deere is recalling about 3,700 ZTrak riding mowers because the blades can rotate while the operator is off the seat, posing a laceration risk.

    Product
    John Deere ZTrak™ riding mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0471-2018·2018-01-31

    BotanicalNow BodySlim Herbal Capsules Recalled for Undeclared Sibutramine

    BotanicalNow is recalling BodySlim Herbal capsules because FDA analysis found undeclared sibutramine, a substance not approved for use in this product.

    Product
    BodySlim Herbal Advanced technology & Strong formula capsules, 400 mg, 30-count bottle, Barcode: 9567153432481
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0343-2018·2018-01-31

    Vyaire Medical Recalls Infant AirLife Humidification Chambers Due to Overflow Risk

    Vyaire Medical is recalling 16,670 Infant AirLife single-limb circuits and humidification chambers because a manufacturing error may cause water to back up into the patient's airway.

    Product
    Infant AirLife single-limb, continuous-flow circuit (Model AH132) containing AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0344-2018·2018-01-31

    Vyaire Medical Recalls Infant AirLife Humidification Chamber Due to Overflow Risk

    Vyaire Medical is recalling 16,670 Infant AirLife humidification chambers because a manufacturing error may cause water to overflow into the patient's airway.

    Product
    Infant AirLife Dual-,limb, dual-heat, high-flow circuit (Model AH265) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0233-2018·2018-01-31

    Pravastatin Sodium Tablets Recalled Due to Foreign Tablet Presence

    International Laboratories, Inc. is recalling Pravastatin Sodium Tablets 10 mg because bottles may contain 20 mg tablets.

    Product
    Pravastatin Sodium Tablets, USP, 10 mg, 30-count bottles, packaged in 12 x 30 tablets for individual patient dispensing per pharmacy dispenser cartons, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-927-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0345-2018·2018-01-31

    Vyaire Medical Recalls Adult Air-Life Single-Limb Circuits Due to Overflow Risk

    Vyaire Medical is recalling 16,670 units of Adult Air-Life single-limb circuits with Humidification Chambers due to a manufacturing error that may cause water overflow into patient airways.

    Product
    Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator gasses to patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0234-2018·2018-01-31

    International Laboratories Recalls Pravastatin Sodium Tablets Due to Foreign Tablets

    International Laboratories, Inc. is recalling Pravastatin Sodium Tablets, 20 mg, because bottles may contain 10 mg tablets. Patients should contact their healthcare provider.

    Product
    Pravastatin Sodium Tablets, USP, 20 mg, 30-count bottles, packaged in 12 x 30 tablets for individual patient dispensing per pharmacy dispenser carton, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-926-16.
    Category
    Drug
    Distribution
    Distributed nationwide