The Recall Desk

State

Louisiana product recalls

73,741 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,965
Critical
1,107
Severe
1,739
Most recent
2026-10-28

Of the 6,965 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 6,965 recalls whose distribution notice names Louisiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36576–36600 of 80706

  • ModerateFDA (Devices)·Z-1718-2019·2019-06-12

    I.T.S. GmbH Recalls Titanium Rim Plates Due to Incorrect Laser Marking

    I.T.S. GmbH is recalling 65 titanium rim plates because they have the wrong article number laser marked on them. The devices were distributed in the US and several international countries.

    Product
    Rim Plate, 10-Hole, Left, PRS RX System. Titanium, implantable - Product Usage: The implant temporarily stabilizes bone segments until bony consolidation has taken place. After this, the implant has no more use and can be removed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1721-2019·2019-06-12

    Kerr/Pentron Recalls Glutaraldehyde Solution Due to Labeling Discrepancy

    Kerr/Pentron is recalling Regimen 28 Day Glutaraldehyde Solution because the bottle label states a 45-minute immersion time, while the product instructions specify 90 minutes.

    Product
    Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
    Category
    Medical Device
    Distribution
    21 states
  • ModerateFDA (Devices)·Z-1733-2019·2019-06-12

    Smith Medical JELCO Hypodermic Needle Recall for Incorrect Specifications

    Smiths Medical ASD Inc. is recalling JELCO Hypodermic Needles with incorrect length and gauge. The recall covers 109,000 units distributed nationwide.

    Product
    Smith Medical JELCO Hypodermic Needle-Pro EDGE Safety Device Safety Device Rx Only Sterile Product Usage: Is a disposable, single use device intended for injection or aspiration of fluids using a Luer lock or Luer slip syringe. The needle protection device covers the needle…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1707-2019·2019-06-12

    NxStage PureFlow B Solution Recalled for Incorrect Product Number Labeling

    NxStage Medical is recalling specific lots of PureFlow B Solution because they were mislabeled with the incorrect product number.

    Product
    NxStage PureFlow B Solution, REF RFP-401, M535RPF4010 NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1709-2019·2019-06-12

    Abbott Recalls Alinity c Cuvette Segments Due to Seating Defect

    Abbott is recalling Alinity c Cuvette Segments because individual cuvettes may seat lower than designed, potentially preventing the sample probe from making efficient contact with the cuvette bottom.

    Product
    Alinity c Cuvette Segments, List Number 04S47-01 Product Usage: The Alinity c Cuvettes are used on the Alinity c system processing module. The Alinity c processing module is a fully automated chemistry analyzer allowing random and continuous access, as well as priority and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1706-2019·2019-06-12

    NxStage PureFlow B Solution Recalled for Incorrect Product Number Labeling

    NxStage Medical is recalling 1,998 units of PureFlow B Solution because certain lots were mislabeled with the incorrect product number.

    Product
    NxStage PureFlow B Solution, REF RFP-400, M535RFP4000 Product NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1730-2019·2019-06-12

    Microbiologics Recalls Cepheid Xpert MRSA Control Panels Due to Incorrect Shelf Life

    Microbiologics Inc is recalling 249 units of Cepheid Xpert MRSA/MRSA NxG and Xpert SA Nasal Complete Control Panels because they have an incorrect shelf life.

    Product
    Cepheid Xpert MRSA/MRSA NxG Control Panel (Catalog #8195) UDI: 70845357041226 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQUIRED: MEDICAL DEVICE CORRECTION emails to their direct US consignees requesting them to complete a MEDICAL DEVICE CORRECTION FORM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1731-2019·2019-06-12

    Microbiologics Recalls Cepheid Xpert SA Nasal Control Panels for Shelf Life Error

    Microbiologics is recalling 235 units of Cepheid Xpert SA Nasal Complete Control Panels due to incorrect shelf life labeling.

    Product
    Cepheid Xpert SA Nasal Complete Control Panel (Catalog #8196) UDI: 70845357041233 Product Usage: On April 9, 2019, Microbiologics sent ACTION REQUIRED: MEDICAL DEVICE CORRECTION emails to their direct US consignees requesting them to complete a MEDICAL DEVICE CORRECTION FORM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1732-2019·2019-06-12

    Smiths Medical Recalls Portex Tracheostomy Tubes with Incorrect Inner Cannula Size

    Smiths Medical ASD Inc. is recalling 7,840 Portex Blue Line Ultra Tracheostomy Tubes because they were packaged with an incorrect size inner cannula.

    Product
    Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part, Product Usage: The Portex Blue Line Ultra¿ Tracheostomy Tubes are indicated for airway maintenance of tracheostomized patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1699-2019·2019-06-12

    Fresenius 2008T BlueStar Hemodialysis Machines Recalled for Power Logic Board Fail Message

    Fresenius Medical Care is recalling 257 units of the 2008T BlueStar hemodialysis machine due to a power logic board fail message on software version 2.72.

    Product
    2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number: 191126 - Product Usage: The 2008T hemodialysis machine is indicated for acute and chronic dialysis therapy in a healthcare facility.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V443000·2019-06-11

    Freightliner M2 and 108SD Trucks Recalled for Axle Lubrication Defect

    Daimler Trucks North America is recalling 2019-2020 Freightliner M2 and 2020 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V444000·2019-06-11

    Thomas Built Buses Recall School Buses Due to Dragging Rear Brakes

    Daimler Trucks North America is recalling specific Thomas Built Buses school buses because the driver-side rear brakes may drag, increasing the risk of smoke and fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V441000·2019-06-11

    Godwin Recalls 2017 Dump Bodies Due to Brake Light Wiring Defect

    Godwin is recalling 2017 dump bodies equipped with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    GODWIN — GODWIN DUMP BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V439000·2019-06-11

    Ford Transit Recall: Modified Glass Roof Hatches May Shatter

    LA West is recalling 2018-2019 Ford Transit vehicles with modified glass roof hatches that may shatter due to stress, posing an injury risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V428000·2019-06-11

    Unicell Recalls ASA Voyager Monitors on Commercial Vehicles

    Unicell is recalling 325 commercial vehicles equipped with ASA Electronics Voyager monitors that may display reversed back-up camera images, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, RAM, ISUZU EXPRESS, PROMASTER, NPR, 155
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19752·2019-06-11

    Amazon Recalls AmazonBasics Ceramic Space Heaters Due to Fire and Burn Hazards

    Amazon is recalling AmazonBasics 1500 Watt Ceramic Space Heaters because they can overheat, posing fire and burn hazards. Consumers should stop using the heaters and contact Amazon for a full refund.

    Product
    AmazonBasics 1500 Watt Ceramic Space Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V436000·2019-06-11

    Entegra Recalls 2020 Motorhomes Due to Steering Shaft Bolt Issue

    Entegra is recalling 2020 Anthem and Cornerstone motorhomes because an insufficiently tightened steering shaft bolt may cause steering failure, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA ANTHEM, CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19751·2019-06-11

    Cushy Form Recalls Folding Mattresses for Fire Hazard

    Cushy Form is recalling about 2,300 folding mattresses sold on Amazon.com because they fail to meet federal flammability standards, posing a fire hazard.

    Product
    Cushy Form folding mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V438000·2019-06-11

    2019 Jeep Renegade Recall for Air Bag Calibration Defect

    Chrysler is recalling 2019 Jeep Renegade vehicles with the Upland trim package because the occupant restraint controller may be miscalibrated, increasing injury risk in crashes.

    Product
    JEEP — JEEP RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V433000·2019-06-10

    Ford Recalls 2013 F-150s for Transmission Downshifting Risk

    Ford is recalling 2013 F-150 trucks with 5.0L or 6.2L engines previously repaired under recall 19V-075 because the transmission may unexpectedly downshift into first gear, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide