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.

44901–44925 of 80775

  • SevereNHTSA·17V637000·2017-10-11

    Nissan Recalls 2012 Versa Hatchbacks for Front Coil Spring Fracture Risk

    Nissan is recalling 2012 Versa Hatchbacks sold in 23 states and D.C. because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0009-2018·2017-10-11

    Pro Bioteks Bio-35 Supplement Recalled for Undeclared Soy Lecithin

    Pro Bioteks Laboratories is recalling Bio-35 dietary supplements because they contain undeclared soy lecithin, a common allergen.

    Product
    Bio35, Vitamin-Mineral Omega Oils Trace Minerals Dietary Supplement, 100 Softgel Capsules. UPC 0-26341-12900-2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0001-2018·2017-10-11

    KIND Dark Chocolate Nuts and Sea Salt Bars Recalled for Undeclared Walnuts

    KIND LLC is recalling Dark Chocolate Nuts and Sea Salt Bars because the outer box fails to declare the allergen walnuts, although individual bars are properly labeled.

    Product
    KIND Dark Chocolate Nuts and Sea Salt Bar-containing 12 /1.4 oz (40 g) bars Box :16.08 oz (480 g) per pack. Box UPC: 02652 17751
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0006-2018·2017-10-11

    Permobil Electric Wheelchair Bases Recalled for Top Plate Assembly Failure

    Permobil is recalling 146 electric wheelchair bases due to a potential failure of the top plate assembly that connects the seating system to the base.

    Product
    Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0005-2018·2017-10-11

    Permobil Recalls Electric Wheelchairs Due to Top Plate Assembly Failure Risk

    Permobil is recalling 5,539 Corpus II electric wheelchairs because the top plate assembly may fail, potentially disconnecting the seating system from the base.

    Product
    Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3237-2017·2017-10-11

    Radiometer AutoCheck5+ Level 2 Quality Control Ampoules Recalled for Inaccurate Results

    Radiometer America is recalling AutoCheck5+ Level 2 quality control ampoules because they may provide incorrect pCO2 and pO2 results.

    Product
    AutoCheck5+, Level 2, specifically designed for Radiometer Americas blood gas analyzers The QUALICHECK+ quality control (QC) ampoules are specifically designed for Radiometer America s blood gas analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0004-2018·2017-10-11

    Inopak Choice Antibacterial Hand Soap Recalled for Potential Bacterial Contamination

    Inopak Ltd is recalling Choice Antibacterial Hand Soap due to GMP deviations and potential bacterial contamination from a pump.

    Product
    Choice Antibacterial Hand Soap, (ethyl alcohol 61%) 800 ml/ 27 fl oz, Universal Valve, Inopak LTD, Ringwood, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0007-2018·2017-10-11

    Implant Direct Recalls Swish Duo-Grip Healing Collars Due to Wrong Component

    Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.

    Product
    Implant Direct Swish Duo-Grip Healing Collar, Length: 3mm, Platform: 4.8 mm, Rx only, Sterile Dental Implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0003-2018·2017-10-11

    Inopak Recalls Mild Healthcare Antibacterial Hand Soap Due to Contamination Risk

    Inopak Ltd is recalling specific batches of Mild Healthcare Antibacterial Hand Soap due to potential bacterial contamination from a defective pump.

    Product
    Mild Healthcare Antibacterial Hand Soap, 6% P.C.M.X., 1000 mL and 2000 mL Disc Pump, 800 mL Universal Valve, and 1 gallon bottles, Inopak. Ltd, Ringwood, NJ 07456
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0001-2018·2017-10-11

    Carl Zeiss INTRABEAM PRS 500 Radiation Therapy Devices Recalled for Calibration Error

    Carl Zeiss Meditec AG is recalling nine INTRABEAM PRS 500 radiation therapy devices because they had incorrect printed calibration values on their certificates.

    Product
    Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0001-2018·2017-10-11

    Pfizer Recalls Deferoxamine Mesylate Injection Due to CGMP Deviations

    Pfizer is recalling 32,276 vials of Deferoxamine Mesylate for injection due to a failure to control impurities causing color change at the API stage.

    Product
    Deferoxamine Mesylate for injection, USP, Single-use Vial, 500 mg/vial, 10 mL vial. Intravenous, Intramuscular, Subcutaneous Use, Rx Only, Hospira, Inc., Lake Forest IL USA, NDC 0406-2336-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V635000·2017-10-09

    Forest River Recalls 2018 Puma Trailers Due to Wheel Tightening Issue

    Forest River is recalling 2018 Puma recreational trailers because wheel center caps may prevent proper tightening, increasing the risk of wheels detaching.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V633000·2017-10-09

    Wabash National Van Trailer Recall for Brake Caliper Bolt Defect

    Wabash National is recalling 2018 Van trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17T017000·2017-10-09

    Harbor Freight Recalls Utility Trailer Tires for Strength Defects

    Harbor Freight is recalling specific Innova and Far East utility trailer tires that may not be strong enough to support expected loads, increasing crash risk.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V634000·2017-10-09

    Thor Motor Coach Recalls 2017-2018 Motorhomes for Incorrect Cargo Labels

    Thor Motor Coach is recalling 2017-2018 motorhomes because incorrect water capacity labels may lead to vehicle overloading and increased crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, THOR MOTOR WINDSPORT, VENETIAN, MIRAMAR, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V631000·2017-10-09

    E-One Recalls 2016-2017 Emergency Vehicles for Steering Defect

    E-One is recalling 2016-2017 Quest, Typhoon, and Cyclone II emergency vehicles because the power steering assist cylinder may not be properly tightened, increasing crash risk.

    Product
    E-ONE — E-ONE QUEST, TYPHOON, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V638000·2017-10-09

    Harbor Freight Recalls Haul Master Trailers Due to Tire Strength Defect

    Harbor Freight is recalling 2014-2017 Haul Master trailers because the tires may not be strong enough to support expected loads, increasing crash risk.

    Product
    HAUL MASTER — HAUL MASTER UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V629000·2017-10-06

    Freightliner Cascadia Recall for Steering Pinch Bolt Tightening Issue

    Daimler Trucks North America is recalling 2017-2018 Freightliner Cascadia vehicles because the upper steering pinch bolt may not be properly tightened, risking loss of steering control.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V625000·2017-10-06

    Subaru Recalls 2015 WRX Models Due to Subwoofer Wiring Fire Risk

    Subaru is recalling 9,178 2015 WRX vehicles because trunk items may cause subwoofer wiring to short, potentially leading to overheating and fire.

    Product
    SUBARU — SUBARU WRX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V632000·2017-10-06

    John Evans Recalls 2017-2018 Flatbed Trailers Due to Brake Defect

    John Evans is recalling 2017-2018 Flatbed trailers because air brake diaphragms may degrade, causing emergency brakes to engage and increasing crash risk.

    Product
    EVANS — EVANS FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide