The Recall Desk

State

Louisiana product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41251–41275 of 80772

  • ModerateFDA (Devices)·Z-2500-2018·2018-08-01

    Philips Centron Medical Imaging Systems Recalled for Shutter Reset Issue

    Philips Healthcare is recalling 459 Centron systems because shutter settings reset when procedure types change, potentially affecting imaging accuracy.

    Product
    Centron Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0979-2018·2018-08-01

    Major Pharmaceuticals Recalls Enalapril Maleate Tablets Due to Impurities

    Major Pharmaceuticals is recalling specific lots of Enalapril Maleate Tablets, 2.5 mg, because the product failed impurity specifications for a degradation product.

    Product
    Enalapril Maleate Tablets, USP, 2.5 mg, 100 Tablets (10 x 10) Unit Dose per carton, Rx only, Manufactured by: Wockhardt Limited, H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0991-2018·2018-08-01

    Aidarex Recalls Enalapril Maleate Due to Out-of-Specification Degradation Product

    Aidarex Pharmaceuticals is recalling specific lots of Enalapril Maleate 5mg due to out-of-specification results for a degradation product during commercial stability.

    Product
    Enalapril Maleate, USP 5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2541-2018·2018-08-01

    Bio-Rad PR4100 Microplate Reader Recalled for Power Supply Connector Risk

    Bio-Rad is recalling 153 PR4100 Microplate Readers because the power supply connector can fit incompatible components, risking irreparable damage to the system.

    Product
    PR4100 Microplate Reader US, Catalog Number 45591587 Product Usage: The PR4100 Microplate Reader is a 96 well absorbance reader for the measurement of light absorbance (optical density-OD) of liquid media. The instrument is intended to be used primarily for the in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2530-2018·2018-08-01

    Human Design Medical Recalls Vivo 65 Ventilators Due to Firmware Issue

    Human Design Medical is recalling 45 Vivo 65 home ventilators because some devices have an unreleased version of the Firmware upgrade tool.

    Product
    Vivo 65, Continuous Ventilator, Home Use, Cat. No. 204000 Product Usage: To provide continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0990-2018·2018-08-01

    Aidarex Recalls Enalapril Maleate 2.5mg Due to Stability Issues

    Aidarex Pharmaceuticals is recalling 11 bottles of Enalapril Maleate 2.5mg because out-of-specification degradation products were found during stability testing.

    Product
    Enalapril Maleate, USP 2.5MG, 90-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0977-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0980-2018·2018-08-01

    Major Pharmaceuticals Recalls Enalapril Maleate Tablets Due to Impurities

    Major Pharmaceuticals is recalling 5,933 cartons of Enalapril Maleate Tablets, 5 mg, due to out-of-specification degradation products.

    Product
    Enalapril Maleate Tablets, USP, 5 mg, 100 Tablets (10 x 10) Unit Dose per carton, Rx only, Manufactured by: Wockhardt Limited, H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ 07054; Distributed…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2529-2018·2018-08-01

    Nobel Biocare Multi-Unit Abutment Recalled for Missing Label Information

    Nobel Biocare is recalling 74 units of Multi-Unit Abutments because the product labels are missing the lot number, expiration date, and other required information.

    Product
    Nobel Biocare 17¿ Multi-Unit Abutment, Conical Connection NP, 2.5mm, REF 36614. Product Usage: Intended to be used in the upper and lower jaw and used for supporting tooth replacements to restore chewing function. The Multi-Unit Abutments, in combination with endosseous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0992-2018·2018-08-01

    Aidarex Recalls Enalapril Maleate Due to Out-of-Specification Degradation Product

    Aidarex Pharmaceuticals is recalling 25 bottles of Enalapril Maleate 5mg due to out-of-specification degradation results during stability testing.

    Product
    Enalapril Maleate, USP 5MG, 30-count bottle, RX only. Packaged By: Aidarex Pharmaceuticals. Mfg: Wockhardt Ltd. India. NDC: 33261-0693-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·18755·2018-07-31

    Matrix Fitness Ascent Trainers and Ellipticals Recalled for Fire Hazard

    Johnson Health Tech is reannouncing a recall of Matrix fitness machines due to a fire hazard caused by moisture buildup in the power socket.

    Product
    Ascent Trainer® by Matrix and Matrix fitness elliptical
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V510000·2018-07-31

    Heartland Sundance XLT TT Recalled for Incorrect Tire Load Rating

    Heartland is recalling 2018 Sundance XLT TT trailers equipped with incorrect Load Range C tires. Owners should contact dealers to replace them with correct Load Range D tires.

    Product
    HEARTLAND — HEARTLAND SUNDANCE XLT TT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V504000·2018-07-31

    Cummins Recalls 2015-2018 Generator Sets Due to Wiring Defect

    Cummins is recalling 2015-2018 generator sets because incorrect wiring may prevent the remote emergency stop from functioning, increasing injury risk.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E065000·2018-07-30

    TAP Recalls Pro Comp Extended Thread Lug Nuts for Seating Issues

    TAP Worldwide is recalling specific Pro Comp Extended Thread Lug Nuts that may not seat properly, potentially causing wheel detachment and loss of vehicle control.

    Product
    WHEELS:LUGS/NUTS/BOLTS/STUDS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V499000·2018-07-30

    Keystone Recalls 2019 Summerland Trailers Due to Propane Bracket Defect

    Keystone is recalling 2019 Summerland recreational trailers because the propane bottle brackets may break, allowing the cylinder to detach and increasing the risk of injury or crash.

    Product
    KEYSTONE — KEYSTONE SUMMERLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E073000·2018-07-30

    TAP Pro Comp Shock Absorbers Recalled for Mounting Defect

    TAP Worldwide is recalling Pro Comp aftermarket shock absorbers because an incorrect lower mount may cause them to detach, affecting vehicle handling and increasing crash risk.

    Product
    SUSPENSION:REAR:SHOCK ABSORBER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E068000·2018-07-30

    TAP Recalls LRG Rims 8-Lug Aftermarket Wheel Center Caps

    TAP Worldwide is recalling LRG Rims 8-Lug aftermarket wheel center caps that may not seat properly, potentially causing wheels to loosen and increasing crash risk.

    Product
    WHEELS:HUB recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E067000·2018-07-30

    TAP Recalls G2 Axle and Gear Wheel Spacers for Missing Hub Rings

    TAP Worldwide is recalling G2 Axle and Gear aftermarket wheel spacers that may lack hub-centering rings, potentially causing wheels to wobble or loosen.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E070000·2018-07-30

    TAP Recalls G2 Axle Housings Due to Potential Weld Failure

    TAP Worldwide is recalling G2 Axle and Gear aftermarket axle housings because weak welds may allow the axle tube to rotate, increasing crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E064000·2018-07-30

    TAP Recalls Pro Comp Steering Knuckles for Nissan Titan Vehicles

    TAP Worldwide LLC is recalling Pro Comp aftermarket steering knuckles for Nissan Titan vehicles because they may deform or fracture under high loads, potentially causing loss of control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V500000·2018-07-30

    Forest River Cherokee Wolf Pup Recalled for Propane Bracket Defect

    NHTSA is recalling 2019 Forest River Cherokee Wolf Pup trailers because a propane bracket may break, causing the cylinder to detach and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE WOLF PUP
    Category
    Vehicle
    Distribution
    Distributed nationwide