The Recall Desk

State

Louisiana product recalls

73,737 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.

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32101–32125 of 80702

  • LowFDA (Devices)·Z-1625-2020·2020-04-08

    Gentell Hydrogel Ag Saturated Gauze Recalled for FDA Registration Deficiency

    Gentell, Inc. is recalling 6,433 units of Gentell Hydrogel Ag Saturated Gauze because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4x8, model no. GEN-11820 - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Saturated Gauze is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers, first and second…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1626-2020·2020-04-08

    Gentell Hydrogel Ag Wound Dressing Recalled for Registration Issues

    Gentell, Inc. is recalling Gentell Hydrogel Ag wound dressings because the product was not properly registered with the FDA.

    Product
    Gentell Hydrogel Ag 4oz. Tube, model no. - Product Usage: Under the care of a healthcare professional, Gentell Hydrogel Ag Silver Antimicrobial Wound Dressing is indicated for partial and full thickness wounds, including pressure ulcers, venous stasis ulcers, diabetic ulcers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V201000·2020-04-07

    Vac-Tron Recalls Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 535, MC 533 SDT, MINICOMBO, MC 573 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V204000·2020-04-07

    Vac-Tron Recalls 2012-2020 Vacuum Excavator Trailers for Lighting Defects

    Vac-Tron is recalling 2012-2020 vacuum excavator trailers because improper exterior lighting and missing reflectors may reduce visibility at night, increasing crash risk.

    Product
    VAC-TRON — VAC-TRON MC 873 SDT, MC 855 SDT, MC 833 SDT, MC 835 SDT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V198000·2020-04-06

    KTM Recalls 2019-2020 790 Adventure Models Due to Rear Brake Hose Overheating

    KTM is recalling 2019-2020 790 Adventure and 790 Adventure R motorcycles because the rear brake hose may overheat, potentially causing brake failure and increasing crash risk.

    Product
    KTM — KTM 790 ADVENTURE R, 790 ADVENTURE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V193000·2020-04-03

    Isuzu Recalls 2019 NPR Vehicles Due to Brake Line Clip Defect

    Isuzu is recalling 2019 NPR and Chevrolet 4500 vehicles because incorrectly installed brake line clips may cause rear driver-side brake failure.

    Product
    ISUZU — ISUZU NPR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V196000·2020-04-03

    Trans Tech Bus Recalls 2020 Models for Seatbelt Warning Light Defect

    Trans Tech Bus is recalling 446 specific 2020 Roadstar, SST, and ST Aero buses because the seatbelt-unfastened warning light may not illuminate for five seconds after ignition.

    Product
    TRANS TECH — TRANS TECH ROADSTAR, SST, ST AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V190000·2020-04-02

    Setra S417TC Coaches Recalled for Front Door Detachment Risk

    Daimler Coaches is recalling 2017-2020 Setra S417TC coaches because the front entrance door support frame may be the wrong size, allowing the door to detach while moving.

    Product
    SETRA — SETRA S417 TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20102·2020-04-02

    Manhattan Toy Recalls Musical Lili Llama Due to Choking Hazard

    Manhattan Toy is recalling Musical Lili Llama wooden activity toys because loose screws can fall off, posing a choking hazard to young children.

    Product
    Musical Lili Llama
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20104·2020-04-02

    VP Harrier and Giant Pinner DH Bicycle Pedals Recalled for Fall Hazards

    VP Components is recalling Harrier and Giant Pinner DH bicycle pedals because the spindle can separate from the pedal body, posing fall and injury hazards.

    Product
    VP Harrier and Giant Pinner DH bicycle pedals
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20105·2020-04-02

    Stelpro Recalls Sonoma Wall Fan Heaters Due to Fire Hazard

    Stelpro Design is recalling about 3,600 Sonoma wall fan heaters because an internal part poses a fire hazard. Consumers should stop using the units and contact Stelpro for a free replacement.

    Product
    ASSO and ASSOS Sonoma wall fan heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V192000·2020-04-02

    KME Emergency Vehicles Recalled for Battery Corrosion Electrical Short Risk

    KME is recalling 2016-2020 emergency vehicles because battery corrosion can cause electrical shorts, potentially draining the battery and preventing operation during emergencies.

    Product
    KME — KME COMMERCIALCAB/ CHASSIS, PREDATOR PANTHER, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1589-2020·2020-04-01

    Medtronic MiniMed Paradigm Insulin Pumps Recalled for Cybersecurity Vulnerabilities

    Medtronic MiniMed is recalling 38 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.

    Product
    Medtronic MiniMed Paradigm Insulin pump, model number MMT-522K
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1528-2020·2020-04-01

    Ev3 Pipeline Flex Embolization Device Recalled for Delivery System Fracture Risk

    Micro Therapeutics is recalling 762 Ev3 Pipeline Flex Embolization Devices because the delivery system may fracture during implantation, potentially leaving parts in the patient.

    Product
    ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1527-2020·2020-04-01

    ev3 Pipeline Flex Embolization Device Recalled for Potential Fracture

    Micro Therapeutics Inc is recalling 1,050 ev3 Pipeline Flex Embolization Devices because the delivery system may fracture during implantation, potentially leaving a part in the patient.

    Product
    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1591-2020·2020-04-01

    Medtronic MiniMed Paradigm Insulin Pump Recalled for Cybersecurity Vulnerabilities

    Medtronic MiniMed is recalling 23,221 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.

    Product
    Medtronic MiniMed Paradigm Insulin pump, model number MMT-523
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1587-2020·2020-04-01

    Medtronic MiniMed Paradigm Insulin Pumps Recalled for Cybersecurity Vulnerabilities

    Medtronic MiniMed is recalling 88,243 Paradigm insulin pumps due to cybersecurity vulnerabilities that could allow unauthorized wireless control of insulin delivery.

    Product
    Medtronic MiniMed Paradigm Insulin pump, model number MMT-522
    Category
    Medical Device
    Distribution
    Distributed nationwide