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.

45301–45325 of 80783

  • SevereFDA (Drugs)·D-1123-2017·2017-08-30

    Rugby Senexon Liquid Recalled for Microbial Contamination

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

    Product
    Rugby Senexon Liquid Natural Vegetable Stimulant,(Sennosides) 8.8 mg, 8 fl oz (237 mL) plastic bottles, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, ?Suite 233, Livonia, MI 48152 --- NDC 0536-1000-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3054-2017·2017-08-30

    Medtronic AxiEM ENT Suction Devices Recalled for Verification Failure

    Medtronic is recalling 60 reusable ENT suction instruments because they fail required pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.

    Product
    Medtronic Suction 9734308 Small AxiEM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3059-2017·2017-08-30

    Custom Assemblies Recalls Custom Surgical Kits with Defective BD Needles

    Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.

    Product
    Various custom surgical kits manufactured for CMS, CUSTOM MEDICAL SPECIALTIES, INC.: (a) CMS-4153-R2 MPM Biopsy TRAY (b) CMS-5832-R1 Custom Safety Mammo Biopsy Tray (c) CMS-4108 Multipurpose Safety Tray (d) CMS-3141-R6 Custom Ultrasound Tray (e) CMS-2891-R1 Custom Safety…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3439-2017·2017-08-30

    Sysco X-Large Jo-Jo Wedges Recalled for Undeclared Milk

    Penobscot McCrum LLC is recalling Sysco X-Large Jo-Jo Wedges because the product may contain undeclared milk.

    Product
    Sysco X-Large Jo-Jo Wedges / 7641749 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighNHTSA·17V538000·2017-08-30

    REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Wiring Defect

    REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER JAMBOREE, VESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3066-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans SFILL 360 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans SFILL 360, 3-TT-SFILL 360. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3049-2017·2017-08-30

    Alcon ORA System Recall for Incorrect IOL Power Measurements

    Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.

    Product
    ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3061-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 250 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3052-2017·2017-08-30

    Medtronic Curved Suction 70 Recalled for Verification Failure

    Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.

    Product
    Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3063-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans Filtron 1000 Due to Seal Integrity

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3437-2017·2017-08-30

    Penobscot McCrum Recalls Seasoned Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Extra Large Seasoned/Battered Jo-Jo Wedges because the product may contain undeclared milk.

    Product
    Extra Large Seasoned/Battered Jo-Jo Wedges / 00148 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3064-2017·2017-08-30

    FDA Recalls Tissu-Trans Filtron 2000 Due to Sterile Seal Integrity Concerns

    Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.

    Product
    Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3438-2017·2017-08-30

    Valero Baby Wedges Recalled for Undeclared Milk

    Penobscot McCrum LLC is recalling Valero Baby Wedges with Crisp Coat UC Coating because the product may contain undeclared milk.

    Product
    Valero Baby Wedges with Crisp Coat UC Coating / 51049 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-3065-2017·2017-08-30

    Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Seal Integrity

    Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.

    Product
    Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3058-2017·2017-08-30

    Medtronic ENT Navigation Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.

    Product
    Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). The firm name on the label is Medtronic Navigation, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3441-2017·2017-08-30

    Penobscot McCrum Recalls Battered Jo-Jo Wedges for Undeclared Milk

    Penobscot McCrum LLC is recalling Medium Battered Jo-Jo Wedges because the product may contain undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Medium Battered Jo-Jo Wedges / 00126 (5 lb bags)
    Category
    Food
    Distribution
    26 states
  • HighNHTSA·17V539000·2017-08-30

    New Flyer Transit Bus Seat Belt Buckle Recall

    New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.

    Product
    NEW FLYER — NEW FLYER MD30, XD40, XN40, MD35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3069-2017·2017-08-30

    Medtronic Recalls Deep Brain Stimulation Lead Kits Due to Depth Stop Defect

    Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.

    Product
    DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and 3391/3391S, The lead kit contains one DBS lead in addition to multiple accessories used in DBS lead implant procedures. Among these accessories is the DBS lead…
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Food)·F-3409-2017·2017-08-30

    Grandma's Herbs Cholesterol Support Recalled for Undeclared Soy Lecithin

    Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.

    Product
    "Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET plastic bottles, UPC# 714938 00046
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17215·2017-08-30

    Dr. Brown's Natural Bottle and Dish Soap Recalled for Bacteria Risk

    Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.

    Product
    Dr. Brown's Natural bottle and dish soap
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3456-2017·2017-08-30

    Lakeside Foods Recalls IQF Green Beans Due to Listeria Risk

    Lakeside Foods, Inc. is recalling 1,856 cases of IQF green beans in 17 states due to potential Listeria monocytogenes contamination.

    Product
    IQF Green Beans, Keep Frozen. 11 varieties, packaged under the following brands and sizes: 1) Bountiful Harvest French Style Green Beans, 1 - 10lb carton/case; 2) GFS French Style Green Beans, 12  32oz (2lb) poly bags per case; 3) Bountiful Harvest Cut Green Beans, 1  20lb…
    Category
    Food
    Distribution
    17 states
  • HighFDA (Devices)·Z-3051-2017·2017-08-30

    Medtronic ENT Suction Devices Recalled for Verification Failure

    Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.

    Product
    Medtronic Straight Suction 9733449 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide