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.

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.

41276–41300 of 80772

  • SevereNHTSA·18V498000·2018-07-30

    Thor Motor Coach Recalls 2018 Ace RVs Due to LP Hose Fire Risk

    Thor Motor Coach is recalling 167 2018 Ace recreational vehicles because a rubber liquid propane hose may sag and contact the tire, creating a fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E066000·2018-07-30

    TAP Pro Comp Aftermarket Control Arms Recalled for Detachment Risk

    TAP Worldwide is recalling specific Pro Comp aftermarket control arms that may detach due to missing or improperly seated circlips, increasing crash risk.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-07302018-1·2018-07-30

    Caito Foods Recalls Beef, Pork, and Poultry Salad and Wrap Products

    Caito Foods LLC is recalling beef, pork, and poultry salad and wrap products due to concerns about Cyclospora contamination. The products were distributed nationwide.

    Product
    Caito Foods, LLC — FSIS Issues Public Health Alert for Beef, Pork and Poultry Salad and Wrap Products due to Concerns about Contamination with Cyclospora
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V497000·2018-07-29

    Mercedes-Benz Metris Recall: Driveshaft Bolts May Loosen

    Daimler Vans USA is recalling 2017-2018 Mercedes-Benz Metris vehicles because driveshaft securing bolts may loosen, potentially causing loss of drive and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V486000·2018-07-27

    RAM Pickup Trucks Recalled for Tailgate Latch Fracture Risk

    Chrysler is recalling 2015-2017 RAM 1500, 2500, and 3500 trucks because the tailgate latch may fracture and open while driving, potentially causing cargo to fall out.

    Product
    RAM — RAM 1500, 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V495000·2018-07-27

    Trail King Recalls 2016-2018 Dolly Trailers Due to Frame Crack Risk

    Trail King is recalling 2016-2018 Dolly trailers because the frame channel may crack, potentially causing the frame rail to separate and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING DOLLY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V496000·2018-07-27

    Hyundai Recalls 2018 Genesis G80 for Passenger Air Bag Sensor Defect

    Hyundai is recalling 2018 Genesis G80 vehicles because the occupant classification system may fail to deactivate the front passenger air bag, increasing injury risk for children.

    Product
    GENESIS — GENESIS G80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18195·2018-07-27

    Hirsch Gift Recalls CloudCharge Wireless Charging Pads Due to Burn Hazard

    Hirsch Gift is recalling about 21,000 CloudCharge Qi Wireless Charging Pads because they can overheat and cause burns. Consumers should stop using the pads and contact the company for a free replacement.

    Product
    CloudCharge Qi Wireless Charging Pads
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18E062000·2018-07-27

    PTL Recalls Recreational Vehicle Doors Due to Latch Adjustment Defect

    PTL Engineering is recalling 3000 and 7000 Series RV entry doors because the latch rod may be improperly adjusted, allowing the door to open while the vehicle is moving.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V492000·2018-07-26

    Chrysler Recalls 2018 Pacifica and 2019 Jeep Cherokee for Transmission Weld Defect

    Chrysler is recalling 2018 Chrysler Pacifica non-hybrid and 2019 Jeep Cherokee vehicles because a transmission component may not be welded properly, which could cause the vehicle to stop moving.

    Product
    JEEP — JEEP, CHRYSLER CHEROKEE, PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V493000·2018-07-26

    Chrysler Recalls 2018 Pacifica Vehicles Due to Axle Assembly Defect

    Chrysler is recalling 2018 Pacifica vehicles because front axle halfshafts may be incorrectly assembled. This defect could cause loss of drive or movement in Park, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V494000·2018-07-26

    2018 Jeep Cherokee Recall for Potential Front Halfshaft Bearing Failure

    Chrysler is recalling 2018 Jeep Cherokee all-wheel-drive vehicles because the right front halfshaft bearing cage may break, potentially causing loss of drive or movement in Park.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V490000·2018-07-26

    Forest River Recalls 2019 Prime Time Crusader Trailers for Incorrect Placard

    Forest River is recalling 2019 Prime Time Crusader fifth-wheel trailers because the Federal Placard lists an incorrect axle weight capacity, which could lead to axle overload and loss of control.

    Product
    PRIME TIME — PRIME TIME CRUSADER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18193·2018-07-26

    Trek Recalls Bontrager Line Pro Bicycle Pedals Due to Fall Hazard

    Trek is recalling Bontrager Line Pro flat bicycle pedals because the spindle can break, posing a fall hazard. No injuries have been reported.

    Product
    Bontrager Line Pro flat bicycle pedals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18194·2018-07-26

    Jimmy Hack Golf Recalls Orange Whip Swing Trainers Due to Injury Hazard

    Jimmy Hack Golf is recalling Orange Whip swing trainers because the weighted orange ball can detach during use, posing an injury risk to users and bystanders.

    Product
    Orange Whip golf swing trainers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2508-2018·2018-07-25

    Medtronic Tri-Staple 2.0 Intelligent Reloads Recalled for Missing Sled Component

    Medtronic is recalling Tri-Staple 2.0 Intelligent Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.

    Product
    Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 mm Vascular/Medium, Item Code SIG30AVM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0943-2018·2018-07-25

    Avella Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns

    Avella of Deer Valley is recalling 500 syringes of ephedrine sulfate due to potential bag leakage and lack of sterility assurance.

    Product
    ePHEDrine Sulfate, USP 50mg in 0.9% Sodium Chloride USP QS 10mL. 50 mg/10 mL (5 mg/mL). Volume: 10 mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-891-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0945-2018·2018-07-25

    Avella Recalls Fentanyl Syringes Due to Potential Leakage and Sterility Concerns

    Avella of Deer Valley is recalling 100 fentanyl syringes due to potential bag leakage and lack of sterility assurance.

    Product
    fentaNYL 5 mcg Citrate, USP 5 mcg in 0.9% Sodium Chloride, USP QS 0.5mL. (10 mcg per mL) 5 mcg in 0.5 mL. Volume: 0.5 mL. Single dose syringe. For Cook Children's Med Ctr. By: Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-210-72
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0962-2018·2018-07-25

    Avella Recalls Phenylephrine IV Bags Due to Sterility Concerns

    Avella of Deer Valley is recalling 120 bags of Phenylephrine 20 mg IV solution due to potential bag leakage and lack of sterility assurance.

    Product
    PHENYLephrine 20 mg (PHENYLephrine HCL (USP) 20 mg, 5% Dextrose (USP) 250 mL) Volume: 252 mL. Single dose bag. For: Vidant Medical Center, By: Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-894-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0965-2018·2018-07-25

    Avella Recalls Phenylephrine Bags Due to Potential Leakage and Sterility Concerns

    Avella of Deer Valley is recalling 40 bags of Phenylephrine 10 mg due to potential leakage that compromises sterility. The product was distributed nationwide.

    Product
    PHENYLephrine 10 mg (PHENYLephrine HCL (USP) 10mg, 0.9% Sodium Chloride (USP) 250 mL. Volume: 251 mL Single dose bag. For: Redlands Community Hospital Pharmacy. BY: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054 NDC 15082-856-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2514-2018·2018-07-25

    Medtronic Recalls Tri-Staple 2.0 Curved Tip Intelligent Reloads

    Medtronic is recalling specific Tri-Staple 2.0 Curved Tip Intelligent Reloads because a missing sled component may prevent staple formation, potentially leading to bleeding or leakage.

    Product
    Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system 30 mm Vascular/Medium, Item Code SIG30ACTAVM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2509-2018·2018-07-25

    Medtronic Endo GIA Vascular Reloads Recalled for Missing Sled Component

    Medtronic is recalling specific Endo GIA 45mm Vascular Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.

    Product
    Endo GIA 45mm Gray Articulating Vascular Reload with Tri-Staple Technology, Item Code EGIA45AV
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2506-2018·2018-07-25

    Endo GIA 60 mm Articulating Vascular/Medium Loading Unit Recalled for Missing Sled

    COVIDIEN MEDTRONIC is recalling Endo GIA 60 mm Articulating Vascular/Medium Loading Units because a missing sled component may prevent staple formation, leading to bleeding or leakage.

    Product
    Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple Technology, Item Code EGIA60AVM
    Category
    Medical Device
    Distribution
    Distributed nationwide