The Recall Desk

State

Louisiana product recalls

73,817 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.

Which agencies issued them

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45276–45300 of 80783

  • ModerateFDA (Devices)·Z-3101-2017·2017-09-06

    Beckman Coulter UniCel DxH Slidemaker Stainer Recall for Fitting Seal Defect

    Beckman Coulter is recalling 310 UniCel DxH Slidemaker Stainer units because a fitting may not completely seal after installation.

    Product
    UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows for adaptation of the smear appearance and stain methodology according to user preferences. Blood smears produced by the Slidemaker portion of the DxH…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3084-2017·2017-09-06

    Alere iScreen Dx Urine Drug Screen Card Recalled for Labeling Error

    Ameditech Inc is recalling Alere iScreen Dx Urine Drug Screen Cards because the kit box label incorrectly identifies PCP instead of TCA as a drug analyte.

    Product
    Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1 IFU insert. The Alere iScreen Dx Drug Screen Card is a rapid urine screening test that can be performed without the use of an instrument. The test utilizes…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17765·2017-09-05

    ASHERANGEL Recalls Children's Sleepwear for Flammability Violations

    ASHERANGEL is recalling about 950 children's nightgowns and pajama sets sold on Amazon.com because they fail federal flammability standards, posing a burn risk.

    Product
    Children's nightgowns and pajama sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V551000·2017-09-01

    2018 Prime Time Tracer Recalled for Incorrect Tire Pressure Placard

    Forest River is recalling 2018 Prime Time Tracer trailers because the Federal Placard may list incorrect tire pressure information, posing a crash risk.

    Product
    PRIME TIME — PRIME TIME TRACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V535000·2017-08-31

    Mack Pinnacle Trucks Recalled for Potential Steering Loss

    Mack is recalling 2016 Pinnacle CHU and CXU diesel trucks because improperly torqued steer axle components may allow the tie rod to loosen, potentially causing a complete loss of steering.

    Product
    MACK — MACK PINNACLE (CXU), PINNACLE (CHU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E049000·2017-08-31

    Meritor Trailer Axle Brake Caliper Bolt Recall

    Meritor is recalling trailer axles and suspensions with EX225 brakes because improperly torqued caliper bolts may allow the caliper to detach, causing a loss of braking ability.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V544000·2017-08-31

    Thor Motor Coach Recalls 2010-2011 Motorhomes Due to Fire Risk

    Thor Motor Coach is recalling 124 Hurricane, Serrano, and Windsport motorhomes because a transfer switch may overheat and cause a fire.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH WINDSPORT, HURRICANE, SERRANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V541000·2017-08-31

    Chrysler Recalls 2017 Dodge Durango for Rear Axle Halfshaft Defect

    Chrysler is recalling 2017 Dodge Durango vehicles because rear axle halfshafts may be too short. This defect can cause a loss of drive and increase the risk of a crash.

    Product
    DODGE — DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V545000·2017-08-31

    Honda Recalls Vehicles with Incorrectly Installed Passenger Air Bag Inflators

    Honda is recalling specific 2006-2012 vehicles where replacement passenger air bag inflators may have been incorrectly installed, potentially causing improper deployment in a crash.

    Product
    ACURA — ACURA, HONDA TSX, CIVIC, INSIGHT, ACCORD CROSSTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V543000·2017-08-31

    Chrysler Recalls Jeep Cherokee for Missing Tire and Rim Label Information

    Chrysler is recalling 2017-2018 Jeep Cherokee vehicles because the certification label is missing required tire and rim size information, which could lead to incorrect tire installation.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V548000·2017-08-31

    Toyota Recalls Lexus and Land Cruiser Vehicles for Air Bag Defect

    Toyota is recalling specific Lexus and Land Cruiser vehicles because they may have incorrect air bags that could fail to deploy in a crash.

    Product
    LEXUS — LEXUS, TOYOTA LX470, LAND CRUISER, LX570
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17216·2017-08-31

    Hallmark Recalls Plush Baby Stacking Toys Due to Choking Hazard

    Hallmark is recalling itty bittys baby plush stacking toys because fabric hats and bows can detach, posing a choking hazard to children.

    Product
    itty bittys® baby plush stacking toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1111-2017·2017-08-30

    Phenobarbital Tablets Recalled Due to Incorrect Strength Labeling

    C. O. Truxton is recalling Phenobarbital 15 mg tablets that were actually 30 mg due to a labeling error.

    Product
    Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1112-2017·2017-08-30

    C. O. Truxton Recalls Phenobarbital Tablets Due to Labeling Error

    C. O. Truxton is recalling specific lots of Phenobarbital Tablets USP, 30 mg, because they may be mislabeled. The FDA classifies this as a Class I recall.

    Product
    Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3406-2017·2017-08-30

    Friendly Farms Key Lime Crunch Tilts Greek Yogurt Recalled for Undeclared Almonds

    Commonwealth Dairy is recalling Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt because it may contain undeclared almond pieces.

    Product
    Friendly Farms Key Lime Crunch Tilts Greek Lowfat Yogurt, 5.3oz plastic cup, Best by date: AUG/26/2017 04-161 and SEP/22/2017 04-161, UPC for this product is 041498239091, Keep refrigerated
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V537000·2017-08-30

    Hymer Aktiv Recalled for Exhaust Pipe Melt Hazard

    Erwin Hymer is recalling 2016-2018 Hymer Aktiv recreational vehicles because the exhaust pipe may melt the rear bumper and wiring, increasing crash and burn risks.

    Product
    HYMER — HYMER AKTIV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1119-2017·2017-08-30

    Rugby Diocto Liquid Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Liquid due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Liquid, Docusate Sodium 50 mg/ 5 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 17177 N. Laurel Park Dr., Suite 233, Livonia, MI 48152 --- NDC: 0536-0590-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1121-2017·2017-08-30

    Major Senna Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Major Senna Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Major Senna Syrup Natural Vegetable Laxative, Sennoside 8.8 mg, 8 fl. oz. (237 mL) plastic bottles, Dist. by: Major Pharmaceuticals, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152 USA. NDC: 00904-6289-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1120-2017·2017-08-30

    Rugby Diocto Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling Rugby Diocto Syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Diocto Syrup, Docusate Sodium 60 mg/15 mL, Stool Softener Laxative, One Pint (473 mL) plastic bottles, Dist. by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150. NDC: 0536-1001-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1122-2017·2017-08-30

    Rugby Aller-chlor Syrup Recalled for Microbial Contamination

    The Harvard Drug Group is recalling 4,715 bottles of Rugby Aller-chlor syrup due to microbial contamination, including yeast and potential B. cepacia.

    Product
    Rugby Aller-chlor (Chlorpheniramine Maleate Syrup, USP), 2 mg, 4 fl. oz. (120 mL) plastic bottles, Distributed by: Rugby Laboratories 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA --- NDC: 0536-1025-47
    Category
    Drug
    Distribution
    Distributed nationwide