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.

49676–49700 of 80793

  • CriticalFDA (Drugs)·D-0223-2017·2016-12-28

    Skinny Bee Diet capsules recalled for undeclared dangerous ingredients

    Love My Tru Body is recalling Skinny Bee Diet capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein.

    Product
    Skinny Bee Diet capsules, 500 mg, packaged in a 60-count bottle
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0730-2017·2016-12-28

    Woodland Foods Recalls Sunflower Seeds for Listeria Contamination

    Woodland Foods is recalling Di Bruno Bros Roasted & Salted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 25 states.

    Product
    Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "DI BRUNO BROS ROASTED & SALTED SUNFLOWER E SEEDS".
    Category
    Food
    Distribution
    25 states
  • CriticalFDA (Food)·F-0888-2017·2016-12-28

    Simply Fresh Fruit Recalls Cantaloupe Mixes Due to Listeria Risk

    Simply Fresh Fruit is recalling cantaloupe and fruit mixes in grape juice because they may be contaminated with Listeria monocytogenes.

    Product
    1 GL PAIL and 2x1 GL/case SFF FRUIT MIX IN GRAPE JUICE, UPC 4294717155
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0896-2017·2016-12-28

    Simply Fresh Fruit Recalls Cantaloupe and Fruit Mixes for Listeria Risk

    Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.

    Product
    1 GL PAIL SYSCO IMP. CANTALOUPE/GRAPE JUICE, UPC 7486562450
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0728-2017·2016-12-28

    Woodland Foods Recalls D'Allesandro Almond Trail Mix Due to Listeria Risk

    Woodland Foods is recalling D'Allesandro Almond Trail Mix because sunflower seeds in the product may be contaminated with Listeria.

    Product
    Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "D'ALLESANDRO ALMOND TRAIL MIX". Product was packaged into 5 lb boxes.
    Category
    Food
    Distribution
    25 states
  • CriticalFDA (Food)·F-0727-2017·2016-12-28

    Woodland Foods Recalls Sunflower Seeds for Listeria Contamination

    Woodland Foods is recalling D'Allesandro Roasted Salted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 26 states.

    Product
    Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "D'ALLESANDRO ROASTED SALTED SUNFLOWER SEEDS ". Product was packaged into 5 lb boxes.
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-0729-2017·2016-12-28

    Woodland Foods Salt-Free Roasted Sunflower Seeds Recalled for Listeria

    Woodland Foods is recalling salt-free roasted sunflower seeds potentially contaminated with Listeria. The product was distributed to food distributors in 25 states.

    Product
    Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "N34D SALT-FREE ROASTED SUNFLOWER SEEDS".
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Drugs)·D-0215-2017·2016-12-28

    Impax Recalls Lamotrigine Tablets Due to Labeling Mixup

    Impax Laboratories is recalling 3,074 boxes of Lamotrigine Orally Disintegrating Tablets because some 200 mg boxes contained 100 mg tablets.

    Product
    Lamotrigine Orally Disintegrating Tablets (ODT), 200 mg, 30 Tablets 3 blisters containing 10 tablets each, Rx only, Manufactured by: Watson Pharma Private Ltd., Verna, Salcette Goa INDIA, Distributed by: Impax Generics, Hayward, CA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0214-2017·2016-12-28

    Virtus Recalls Hyoscyamine Sulfate Tablets Due to Potency Failures

    Virtus Pharmaceuticals is recalling 24,444 bottles of Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in inconsistent drug potency.

    Product
    Hyoscyamine Sulfate, USP Tablets, 0.125 mg, 100-count tablets per bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-308-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0902-2017·2016-12-28

    Simply Fresh Fruit Recalls Cantaloupe and Fruit Mixes Due to Listeria Risk

    Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.

    Product
    **1) 1 GL CVF FRUIT SALAD DELUXE - LS, UPC #5075810 8449874; **2) 1 GL CVF FRUIT SALAD DELUXE - LS, UPC #50758108449904; **3) 1 GL CVF FRUIT SALAD DELUXE - LS, UPC 50758108449874 ; **4) 1 GL CVF FRUIT SALAD DELUXE - LS, UPC 50758108449874 ; **5) 1 GL CVF FRUIT SALAD…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0726-2017·2016-12-28

    Woodland Foods Recalls Salt-Free Roasted Sunflower Seeds for Listeria Risk

    Woodland Foods is recalling D'Allesandro Salt-Free Roasted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 26 states.

    Product
    Product is packaged into a plastic bag and placed into cardboard box. Product is labeled as "D'ALLESANDRO SALT-FREE ROASTED SUNFLOWER SEEDS". Product was packaged into 5 & 40 lb boxes.
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Drugs)·D-0222-2017·2016-12-28

    3rd Degree Capsules Recalled for Undeclared Sibutramine

    Making It a Lifestyle is recalling 3rd Degree capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.

    Product
    3rd DEGREE capsules, 60-count bottles, Manufactured for: Making it A Lifestyle, L.L.C.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0213-2017·2016-12-28

    Virtus Recalls Hyoscyamine Sulfate Tablets Due to Content Uniformity Failures

    Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in both superpotent and subpotent doses.

    Product
    Hyoscyamine Sulfate, Orally Disintegrating Tablets, 0.125 mg, 100-count bottles, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-307-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0766-2017·2016-12-28

    Chaos and Pain Recalls Cannibal Ferox Amped Pre-Workout Supplement

    Chaos and Pain is recalling its Cannibal Ferox Amped pre-workout supplement because it contains an undeclared prohibited substance.

    Product
    CANNIBAL FEROX AMPED, FACE-MELTING NOOTROPIC, PRE-WORKOUT ENERGY COMPLEX, STRAWBLOODY KIWI CRUSH, DIETARY SUPPLEMENT, NET. WT. 9.9 OZ (280g), Chaos and Pain, UPC 1056331460
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0762-2017·2016-12-28

    Naturecom Recalls DMAA Powder Due to Potential Presence of 1,3-Dimethylamylamine

    Naturecom is recalling 500g bags of DMAA powder because the product may contain 1,3-dimethylamylamine. The recall covers products distributed nationwide and internationally.

    Product
    DMAA (1,3-Dimethylamylamine) Net Weight 500g Product is packaged in approximately 8" x 11 silver and clear mylar ziplock bags that contain 500g of DMAA.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0782-2017·2016-12-28

    FDA Recalls Ultroid Hemorrhoid Management Systems for Quality System Deficiencies

    The FDA is recalling Ultroid Hemorrhoid Management Systems because they were not manufactured under required quality system controls.

    Product
    Ultroid Hemorrhoid Management Systems 110/220 VAC and procedures kit including the Ultroid Disposable Sterile Probes
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Food)·F-0900-2017·2016-12-28

    Simply Fresh Fruit Recalls Cantaloupe and Fruit Mixes for Listeria Risk

    Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.

    Product
    1 GL CVF FRUIT SALAD DELUXE IN GRAPE JUICE, UPC 50758108455745
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0887-2017·2016-12-28

    Amendia Recalls Black Widow Spinal Screws Due to Mating Feature Defect

    Amendia, Inc. is recalling 96 units of Black Widow 6.6mm spinal screws due to a design defect in the mating feature between the plate and screw.

    Product
    Black Widow 6.6mm x 20mm Screw, Part Number TBS020; Black Widow 6.6mm x 25mm Screw, Part Number TBS025; Black Widow 6.6mm x 30mm Screw, Part Number TBS030 The Black Widow Buttress Plates and Screws are designed for preventing migration or expulsion of allograft or autograft in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0832-2017·2016-12-28

    Samuel Adams Apple Hard Cider Recalled for Bottle Bursting Risk

    Samuel Adams Brewery is recalling Apple Orchard Crisp Apple Hard Cider because bottles may burst due to re-fermentation.

    Product
    Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Loose case = 24  12 oz bottles ¿ 12 pack = 12  12 oz bottles, shipped as 2  12 packs per case ¿ 4  6 pack = 6  12 oz bottles per pack, shipped as 4  6 packs per case
    Category
    Food
    Distribution
    22 states
  • SevereFDA (Devices)·Z-0889-2017·2016-12-28

    Medtronic Recalls Clearify Visualization Systems Due to Sterility Compromise

    Medtronic is recalling 1,293,169 Clearify Visualization Systems because a breach of the sterile barrier compromises product sterility.

    Product
    Covidien Clearify Visualization System Item Code: 21-345 Intended to be used prior to and during endoscopic and laparoscopic procedures to prevent fogging of the scope as well as clean the scope lens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0217-2017·2016-12-28

    Novo Nordisk Recalls GlucaGen HypoKits Due to Detached Needles

    Novo Nordisk is recalling 71,215 GlucaGen HypoKits because the syringe needles may be detached. The recall covers lots expiring in September 2017.

    Product
    GlucaGen HypoKit (glucagon [rDNA origin] for injection), 1 mg per vial, Single use only, Rx Only, Manufactured by: Novo Nordisk A/S 2880 Bagsvaerd, Denmark, NDC 0169-7065-15
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0212-2017·2016-12-28

    Virtus Recalls Hyoscyamine Sulfate Tablets Due to Content Uniformity Failures

    Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate sublingual tablets because they failed content uniformity specifications, resulting in tablets that are either superpotent or subpotent.

    Product
    Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-309-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0900-2017·2016-12-28

    Exactech Recalls Equinoxe Reverse Shoulder Screw Kits Due to Disengaged Heads

    Exactech, Inc. is recalling 2,278 Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kits because disengaged screw heads may not be retained in the screwdriver.

    Product
    Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide