The Recall Desk

State

Louisiana product recalls

72,936 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,922
Critical
1,094
Severe
1,483
Most recent
2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2801–2825 of 79858

  • HighFDA (Devices)·Z-1569-2026·2026-03-25

    GE Centricity Viewer 7.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 7.0 through 7.0 Sp2.0.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 5826659-027, 5826659-029, 5826659-032, 5826659-033, 5826659-028, 5826659-034, 5826659-030, 5826
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1586-2026·2026-03-25

    Hologic Aptima HPV assay may produce invalid or false negative results

    Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.

    Product
    Brand Name: Aptima HPV Assay Product Name: Aptima HPV Assay Model/Catalog Number: 303585 Product Description: Aptima HPV assay Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2026·2026-03-25

    GE Centricity Viewer 6.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1565-2026·2026-03-25

    Abbott ID NOW influenza test lot shows higher invalid result rates

    Abbott is recalling one lot of the ID NOW Influenza A & B 2 test after confirming the lot has a higher occurrence of invalid rates than stated in the Instructions for Use.

    Product
    Product Name: ID NOW" Influenza A & B 2 Model/Catalog Number: 427-000 Software Version: Not Applicable Product Description: Influenza A/B virus nucleic acid IVD, kit, nucleic acid technique Component: Not Applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1585-2026·2026-03-25

    Stago D-dimer assay shows positive bias across entire analytical range

    Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.

    Product
    Brand Name: STA Liatest D-Di Product Name: STA Liatest D-Di Model/Catalog Number: REF 00515 Product Description: in vitro diagnostic. The STA - Liatest D-Di kit is an assay for the quantitative determination of D-dimer in venous plasma for use on STA-R, STA Compact and STA Sat
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423657 may leak

    ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423657, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423657 10-35mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0407-2026·2026-03-25

    Brimonidine and timolol eye drops recalled over sterility assurance failure

    Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.

    Product
    BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION — BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION (BRIMONIDINE TARTRATE AND TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0571-2026·2026-03-25

    Miss Vickies Spicy Dill Pickle chips recalled for undeclared milk allergen

    Frito-Lay North America is recalling Miss Vickies Spicy Dill Pickle 8 oz bags that contain undeclared milk allergen. Affected products were distributed in Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, and Texas.

    Product
    Miss Vickies Spicy Dill Pickle; 8 oz bag
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1573-2026·2026-03-25

    Welch Allyn vision screener display may flicker inducing photosensitive seizures

    Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.

    Product
    Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit pe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1571-2026·2026-03-25

    GE Centricity Viewer 5.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 5.0 SP6 through UV 5.0 SP7.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-026, 2088026-115, 2088026-043, K2042VJED, 2088026-132, 2088026-003, 2088026-110, 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1582-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423643 may leak

    ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423643, 10-45mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V187000·2026-03-25

    Aston Martin DBX tire pressure warning light may not illuminate

    Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.

    Product
    ASTON MARTIN — ASTON MARTIN DBX, DBX S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V185000·2026-03-25

    Volkswagen Jetta and Taos instrument panels may not display warnings

    Volkswagen is recalling certain 2025 Jetta and Taos vehicles because the instrument panel may fail to display warning lights or gauges. This fails FMVSS 101.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0398-2026·2026-03-25

    Dexamethasone injection failed impurity specifications at product expiry testing

    Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2026·2026-03-25

    Artegraft vascular graft recalled over incorrect lot outer packaging labeling

    LeMaitre Vascular is recalling one Artegraft Vascular Graft, REF AG740, because of a labeling mix-up resulting in the incorrect lot outer packaging of the product.

    Product
    Artegraft Vascular Graft; REF#: AG740;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1580-2026·2026-03-25

    Stryker Cub pediatric cribs sold in USA missing two warning labels

    Stryker is recalling Cub Pediatric Cribs, model FL19H, because cribs sold in the USA are missing two access door warning labels.

    Product
    Cub Pediatric Crib, Model FL19H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2026·2026-03-25

    Cardiosave battery charging station left bay screw prevents full battery insertion

    Datascope is recalling the Battery Charging Station, model 0998-00-0802, because a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging.

    Product
    Battery Charging Station; Model: 0998-00-0802;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V182000·2026-03-24

    Nova Bus driver seat belt tension device may not disengage

    Nova Bus is recalling certain 2016-2023 LFS and LFS Artic transit buses because the driver's seat belt tension-relieving device may fail to disengage without manual intervention. This fails FMVSS 208.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V180000·2026-03-24

    Lexus LX Recall: Front Passenger Air Bag May Deploy Improperly

    Toyota is recalling 2022-2024 Lexus LX vehicles because a seat frame issue may cause the front passenger air bag to deploy incorrectly during a crash.

    Product
    LEXUS — LEXUS LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V179000·2026-03-24

    2024–2026 Toyota and Lexus vehicles load carrying capacity label incorrect

    Toyota is recalling certain 2024–2026 Toyota and Lexus vehicles because the load carrying capacity modification label may display inaccurate added weight values. Vehicles with incorrect maximum capacity weight may be overloaded, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, TACOMA HYBRID, GRAND HIGHLANDER, CROWN SIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V177000·2026-03-23

    Winnebago motorhome front turn signal lenses are smaller than required

    Winnebago is recalling certain 2017-2022 Brave, Itasca Sunova, Adventurer and Sunstar motorhomes because the front turn signals may have a smaller than required luminous lens area. This fails FMVSS 108.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ADVENTURER, BRAVE, SUNSTAR, SUNOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide