The Recall Desk

State

Louisiana product recalls

73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,967
Critical
1,107
Severe
1,740
Most recent
2026-11-14

Of the 6,967 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 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54826–54850 of 80800

  • SevereFDA (Food)·F-0679-2016·2016-03-09

    Dole Recalls Salads from Springfield, Ohio Facility Due to Operational Suspension

    Dole is withdrawing all salads produced in Springfield, Ohio, to suspend operations at the facility. Consumers should identify affected products by a code starting with 'A'.

    Product
    Asian Island Crunch, 13 oz. bag, Dole brand. All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0662-2016·2016-03-09

    Dole Recalls Salads Produced at Springfield, Ohio Facility

    Dole is withdrawing all salads produced at its Springfield, Ohio facility due to a safety concern. Consumers should check for specific product codes.

    Product
    Greener Supreme , 12 oz. bag - Kroger; Greener Selection, 12 oz. bag - Dole Value Size Greener Selection , 18 oz. bag - Dole All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0672-2016·2016-03-09

    Dole Recalls Salads from Springfield Ohio Facility Due to Safety Concerns

    Dole is withdrawing all salads produced at its Springfield, Ohio facility, including Dole and private label brands, due to a safety issue.

    Product
    Baby Arugula with Spinach Clamshell, 5 oz. clamshell, Dole brand. . All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0673-2016·2016-03-09

    Dole Recalls Salads from Springfield Ohio Facility Due to Safety Concerns

    Dole Fresh Vegetables Inc is withdrawing all Dole and private label salads produced at its Springfield, Ohio facility. Consumers should identify affected products by a code beginning with the letter A.

    Product
    Baby Romaine, 5 oz. clamshell, Dole brand. . All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1031-2016·2016-03-09

    Mako Surgical Recalls Restoris Knee Implants Due to Packaging Damage

    Mako Surgical Corporation is recalling 146 units of the Restoris Multicompartmental Knee System because damaged packaging may have compromised the sterile barrier.

    Product
    Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for single or multi-compartmental knee replacement used in conjunction with RIO.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2016·2016-03-09

    Cook Inc. Recalls Kopans Breast Lesion Localization Needles

    Cook Inc. is recalling 134 Kopans Breast Lesion Localization Needles because they may have been exposed to body fluids during processing, posing a potential risk of blood-borne pathogen transmission.

    Product
    Kopans Breast Lesion Localization Needle The Kopans Breast Lesion Localization Needle consists of a bevel-tip needle with centimeter markings and a hookwire. The hookwire features a burnish mark that allows the operator to ensure that the hookwire is within the needle tip…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1022-2016·2016-03-09

    Philips Recalls BrightView XCT Gamma Cameras Due to Mechanical Defects

    Philips is recalling 427 BrightView XCT gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.

    Product
    BrightView XCT & BrightView XCT Upgrade, gamma cameras; For Single Proton Emission Computed Tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1026-2016·2016-03-09

    Ivoclar Vivadent Recalls Helioseal Clear Pit and Fissure Sealant

    Ivoclar Vivadent is recalling Helioseal Clear dental sealant because a production error may prevent the material from curing properly under specific lights.

    Product
    Helioseal Clear Refill 1 x 1.25 g, REF/Product Code/Art. No. 558521AN and Helioseal Clear Assortment 5 x 1.25 g, REF/Product Code/Art. No. 558520AN ---- COMMON/USUAL NAME: Pit & Fissure Sealant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1044-2016·2016-03-09

    ConvaTec Recalls Opti-Mist Nebulizer Masks Due to Reduced Aerosol Output

    ConvaTec is recalling Opti-Mist and Opti-Mist Clear nebulizer masks because a component defect reduces or stops aerosol output, potentially preventing patients from receiving medication.

    Product
    Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses that are delivered directly to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1021-2016·2016-03-09

    Philips Recalls BrightView X Gamma Cameras Due to Motion and Collision Issues

    Philips Medical Systems is recalling 117 BrightView X gamma cameras worldwide due to potential gantry motion halts and collimator contact with the patient pallet.

    Product
    BrightView X are gamma cameras; Designed for single or dual detector nuclear imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16116·2016-03-09

    Z Gallerie Recalls Golda Wall Clocks Due to Fire Hazard

    Z Gallerie is recalling Golda wall clocks because defective battery springs can cause batteries to overheat, posing a fire hazard.

    Product
    Golda Wall Clocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1020-2016·2016-03-09

    Philips Recalls BrightView Gamma Cameras Due to Motion and Collision Issues

    Philips Medical Systems is recalling 677 BrightView gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.

    Product
    BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2016·2016-03-09

    Aesculap Recalls Mislabelled Knee Implant Packaging for Cementless Use

    Aesculap Inc. is recalling 1,232 units of Columbus Revision and EnduRo Knee System packaging labeled as cementless, which are indicated for use with bone cement only.

    Product
    Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0735-2016·2016-03-09

    Sun Pharma Recalls Alendronate Sodium Tablets Due to Impurity Levels

    Sun Pharma Global Fze is recalling specific lots of Alendronate Sodium Tablets 70 mg because unknown impurity levels exceeded specifications during stability testing.

    Product
    Alendronate Sodium Tablets, USP, 70 mg*, 4-count blisters per carton, Rx only, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; NDC 41616-638-68, UPC 3…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2016·2016-03-09

    Novadaq PINPOINT Endoscopic Imaging System Recalled for Manual Error

    Novadaq is recalling 110 PINPOINT Endoscopic Fluorescence Imaging Systems because the operator's manual lacks validated sterilization parameters for specific components.

    Product
    PINPOINT Endoscopic Fluorescence Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1039-2016·2016-03-09

    Stryker AccuPlace Drace Stereotaxic Needle Guide Recalled for Packaging Sterility Risk

    Stryker is recalling AccuPlace Drace Stereotaxic Needle Guides because packaging defects may breach sterility. The recall covers 5,800 units distributed nationwide.

    Product
    50000 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1038-2016·2016-03-09

    Stryker AccuPlace Round Level Needle Guide Recalled for Sterility Breach Risk

    Stryker is recalling AccuPlace Round Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.

    Product
    (Stryker) AccuPlace Round Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2016·2016-03-09

    Volcano R-100 Sterile Equipment Covers Recalled for Incorrect Expiry Date Labeling

    Volcano Corporation is recalling R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.

    Product
    Volcano R100 Sterile Equipment Cover; Sterile; General Hospital: These Sterile Equipment covers are provided to cover equipment that is mean to be used in the sterile surgical field but cannot be sterilized. The sterile drapes are put over this equipment in case any sterile…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1023-2016·2016-03-09

    Medtronic Perfusion Tubing Packs Recalled Due to Cuvette Safety Alert

    Medtronic is recalling specific lots of Perfusion Tubing Packs because they contain Terumo CVS cuvettes subject to an Urgent Safety Alert.

    Product
    Medtronic Custom Perfusion Tubing Pack, Rx, Sterile EO. Terumo Cardiovascular Systems (Terumo CVS) has distributed an Urgent Safety Alert regarding the CD I¿ H/S Cuvette. The cuvette is packaged into Medtronic Perfusion Tubing Packs and only sold as part of the pack. This…
    Category
    Medical Device
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-1037-2016·2016-03-09

    Stryker AccuPlace Needle Guide Recalled for Sterility Breach Risk

    Stryker is recalling AccuPlace Straight Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.

    Product
    (Stryker) AccuPlace Straight Level Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1036-2016·2016-03-09

    Medical Action Industries Recalls PICC/CVC Dressing Kits Due to Misbranding

    Medical Action Industries is recalling 180 PICC/CVC Secure Dressing Change kits because the presence of CHG is not identified on the exterior labeling.

    Product
    PICC/CVC Secure Dressing Change kit, Ref: 73775, Lot 213403, Sterile Single Use, Medical Action Industries, Inc., Arden, NC. This kit is used by clinicians to change dressings
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1040-2016·2016-03-09

    Stryker AccuPlace Drace Stereotaxic Needle Guide Recalled for Sterility Risk

    Stryker is recalling 5,800 AccuPlace Drace Stereotaxic Needle Guides due to a potential breach in sterility caused by packaging damage.

    Product
    50001 (Inrad) AccuPlace Drace Stereotaxic Needle Guide; Assists the user with inserting a needle at a predetermined angle for computer tomography.
    Category
    Medical Device
    Distribution
    Distributed nationwide