The Recall Desk

State

Louisiana product recalls

73,588 recalls have nationwide distribution and so reach Louisiana. 6,960 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,960
Critical
1,107
Severe
1,739
Most recent
2026-10-21

Of the 6,960 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 1,739 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,960 recalls whose distribution notice names Louisiana specifically. The 73,588 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27851–27875 of 80548

  • SevereFDA (Devices)·Z-1193-2021·2021-03-24

    Medtronic Infant Tubingset Recalled for Elevated Bacterial Endotoxin Levels

    Medtronic is recalling 14 units of infant tubingsets due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack Infant Tubingset Pixie Flow 0,8->1,5-1,8 1/B (PERFUSION M483203D 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V205000·2021-03-24

    Tracker Recalls 2021 Trailers Due to Tire Fender Rubbing

    Tracker Marine is recalling 2021 Ranger Trail and Trailstar trailers because tires may rub against fenders, causing premature wear and increasing the risk of a tire blowout.

    Product
    TRAILSTAR — TRAILSTAR, RANGER TRAIL ZV20, NZ19, NZ21, NZ18
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1198-2021·2021-03-24

    Medtronic Pediatric Cardiotomy Reservoir Recalled for Bacterial Endotoxin

    Medtronic is recalling 4 units of a pediatric cardiotomy reservoir due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.

    Product
    Medtronic Custom Pack CP 1/4-1/4 Pediatric Set 1/B (PERFUSION M484901D 1/B). The Affinity Pixie Cardiotomy/Venous Reservoir (CVR) with Balance Biosurface is a single-use device designed to collect and store blood during extracorporeal circulation. Cardiotomy blood is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V202000·2021-03-24

    2020-2021 Ford F-53 and F-59 Motorhome Rear Bearing and Axle Defect

    Ford is recalling certain 2020-2021 F-53 and F-59 motorhome and commercial chassis vehicles due to inadequate rear axle lubricant. The defect may cause rear wheel bearing damage, rear axle failure, and loss of motive power and brake function.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V206000·2021-03-24

    Western Star 4700 and 5700 Ground Harness Wiring Defect

    DTNA is recalling 2019-2021 Western Star 4700 and 5700 vehicles with undersized ground harness wiring that may cause connector melting and engine stall, increasing crash risk. Owners should contact DTNA for free replacement.

    Product
    WESTERN STAR — WESTERN STAR 5700, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1269-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because table fastening bolts may loosen, causing the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000V Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1273-2021·2021-03-24

    Philips CT Systems Recalled for Potential Couch Movement Failure

    Philips is recalling 109 CT systems because a defect in the Incisive CT couch actuators could cause the couch to fail to self-lock and move downward unexpectedly.

    Product
    Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) applications - Product Usage: intended for use in the head and whole body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1276-2021·2021-03-24

    Epimed Feth-R-Kath Catheter Recalled for Coating Deterioration

    Epimed International is recalling Feth-R-Kath Catheters because the outer coating may crack or flake off. The recall covers 5,835 units distributed nationwide.

    Product
    Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to placement of 72 hours or less
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1253-2021·2021-03-24

    Siemens SOMATOM CT Software Recall for Workflow Interruptions

    Siemens is recalling specific software versions for SOMATOM CT systems due to sporadic errors that may interrupt scanning workflows and delay diagnosis.

    Product
    Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed tomography systems as follows: SOMATOM go.Now (Model 11061610)SOMATOM go.Up (Models 11061620 & 11061628) SOMATOM go.All (Model 11061630) SOMATOM go.Top (Models 11061640 & 11061648) SOMATOM go.Sim…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1254-2021·2021-03-24

    Mindray BeneVision Distributed Monitoring System Recalled for Intermittent Freezes

    Mindray is recalling 1,938 BeneVision Distributed Monitoring Systems because they may intermittently freeze, causing telemetry data to stop communicating to the central system.

    Product
    Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when used with the following software versions: 03.04.00 04.01.00 04.03.00 04.04.00 04.04.01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1272-2021·2021-03-24

    Accuray CyberKnife Treatment Delivery System Recalled for Loose Set Screws

    Accuray is recalling 243 CyberKnife Treatment Delivery Systems because set screws can loosen, allowing the treatment couch to roll unexpectedly.

    Product
    CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V208000·2021-03-24

    2021 Genesis GV80 High-Pressure Fuel Tube Recall: Fire Risk

    Hyundai is recalling certain 2021 Genesis GV80 and G80 vehicles with 2.5-liter turbo engines due to a high-pressure fuel tube that may not seal properly, potentially allowing fuel to leak and increase fire risk.

    Product
    GENESIS — GENESIS GV80, G80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Pack Recall for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagent Packs used with Remel M4RT Viral Transport Media due to potential false reactive results.

    Product
    VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent immunoassay intended for the qualitative detection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2021·2021-03-24

    Canon Medical Recalls Catheterization Tables Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because loose bolts may cause the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V207000·2021-03-24

    2021 Thomas Built Buses Saf-T-Liner C2 Recalled for Damaged Valve Stems

    Daimler Trucks North America is recalling 2021 Thomas Built Buses Saf-T-Liner C2 school buses because tire valve stem extensions may be damaged by brake calipers, risking tire pressure loss.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V199000·2021-03-24

    2021 BMW X3 and X4 Fuel Tank Weld May Separate, Increasing Fire Risk

    BMW is recalling certain 2021 X3 and X4 vehicles due to a fuel tank weld that may fail, allowing fuel to leak and increasing fire risk. All repairs have been completed.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1268-2021·2021-03-24

    Carestream Dental CS 3600 Tips Recalled for Detachment Risk

    Carestream Dental is recalling CS 3600 Single Use Normal Tips because the mirror may become detached and fall from the unit.

    Product
    Carestream Dental CS 3600 Single Use Normal Tips, Catalog Number 5941216 - Product Usage: used to record the topographic characteristics of teeth or dental impressions in three dimensions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1275-2021·2021-03-24

    Sirtex Medical Recalls SIROS D-Vial Prep Sets Due to Particulate Matter

    Sirtex Medical Limited is recalling SIROS D-Vial Prep Sets because of a potential presence of particulate matter in the D-Vial.

    Product
    SIROS D-Vial Prep Set, Product Code SIR-10200 - Product Usage: intended for single use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V209000·2021-03-24

    2021 Western Star 4700 and Freightliner Cascadia clutch assembly recall

    Daimler Trucks North America recalls certain 2021 Western Star 4700 and Freightliner Cascadia vehicles because the clutch flange may break, causing clutch disengagement and crash risk. Dealers will replace the clutch assembly free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 interventional angiography systems because the table may tilt if fastening bolts become loose.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1266-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Recalled for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagents because they may produce false reactive results when used with Remel M4RT Viral Transport Media.

    Product
    VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro Diagnostic. The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1251-2021·2021-03-24

    Cardinal Health Recalls McKesson Prevent M Needles Due to Safety Shield Defect

    Cardinal Health is recalling 108,000 McKesson Prevent M needles because the safety shield may fail to lock, posing a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1250-2021·2021-03-24

    Cardinal Health Recalls Magellan Hypodermic Safety Needles Due to Locking Failure

    Cardinal Health is recalling Magellan Hypodermic Safety Needles because the safety shield may fail to lock, creating a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    Magellan Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881850558
    Category
    Medical Device
    Distribution
    Distributed nationwide