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.

37576–37600 of 80706

  • HighFDA (Devices)·Z-1056-2019·2019-04-03

    Philips URODiagnost Eleva X-ray System Recalled for Missing Locking Plate

    Philips North America, LLC is recalling URODiagnost Eleva X-ray systems because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.

    Product
    URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system with remote-controlled facilities. It performs a wide range of routine examinations and interventional procedures include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1052-2019·2019-04-03

    Philips MultiDiagnost-Eleva Imaging System Recalled for Missing Locking Plate

    Philips is recalling MultiDiagnost-Eleva imaging systems because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.

    Product
    MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application system, General RIF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications on human patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1057-2019·2019-04-03

    Lupin Recalls Fayosim Tablets Due to Impurity Test Failures

    Lupin Pharmaceuticals is recalling specific lots of Fayosim tablets because they failed impurity specifications during stability testing.

    Product
    Fayosim (levonorgestrel and ethinyl estradiol) tablets USP, (0.15 mg/0.02 mg, 0.15 mg/0.025 mg, 0.15 mg/0.03 mg) and ethinyl estradiol tablets USP, (0.01 mg), packaged in 1 Extended-Cycle Wallet of 91 Tablets packed in a pouch(NDC 68180-860-11); one pouch per carton (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1060-2019·2019-04-03

    Ecolab Gel Hand Sanitizer Recalled for Chemical Contamination

    Ecolab Inc. is recalling specific lots of Ecolab Gel Hand Sanitizer due to the presence of low levels of substituted benzene compounds.

    Product
    ECOLAB — ECOLAB (ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1063-2019·2019-04-03

    Ecolab Recalls Quick-Care Foam Hand Sanitizer Due to Chemical Contamination

    Ecolab is recalling 67 units of Quick-Care Foam Hand Sanitizer due to low levels of substituted benzene compounds found after malodor complaints.

    Product
    Quick-Care Foam Hand Sanitizer (Ethyl alcohol 62%), 45 mL (1.5 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-491-85
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1061-2019·2019-04-03

    Ecolab Recalls Advanced Gel Hand Sanitizer Due to Chemical Contamination

    Ecolab is recalling Advanced Gel Hand Sanitizer because low levels of substituted benzene compounds were found after complaints of malodor.

    Product
    ADVANCED GEL HAND SANITIZER — ADVANCED GEL HAND SANITIZER (ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1064-2019·2019-04-03

    Ecolab Recalls Express Gel Hand Sanitizer Due to Chemical Contamination

    Ecolab is recalling 105 bottles of Express Gel Hand Sanitizer due to low levels of substituted benzene compounds found after malodor complaints.

    Product
    Express Gel Hand Sanitizer (Ethyl Alcohol 70%), 37 mL (1.25 fl oz) bottles, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102. NDC 47593-502-49
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1058-2019·2019-04-03

    Ingenus Recalls Diclofenac Sodium Topical Solution Due to Leaking Bottles

    Ingenus Pharmaceuticals is recalling 29,435 bottles of Diclofenac Sodium Topical Solution because some bottles were found leaking.

    Product
    Diclofenac Sodium Topical Solution, 1.5% w/w, 5 FL. OZ. (150 mL) bottle, Rx Only, Manufactured for: Ingenus Pharmaceuticals, LLC, Orlando, FL 32839-6408, NDC 50742-308-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1073-2019·2019-04-03

    CryoLife Recalls Two On-X Aortic Heart Valves for Mislabeled Serial Numbers

    CryoLife, Inc. is recalling two On-X Aortic Heart Valves because they were mislabeled with incorrect serial numbers. The devices were distributed in Georgia and Germany.

    Product
    On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: The On-X Prosthetic Heart Valve is indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic position. It is a bileaflet mechanical heart valve, which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V265000·2019-04-02

    Entegra Recalls 2019 Vision and Emblem Motorhomes for Fire Risk

    Entegra Coach is recalling 2019 Vision and Emblem motorhomes because a missing fuse in the blower motor circuit may cause wiring to overheat and increase the risk of fire.

    Product
    ENTEGRA — ENTEGRA VISION, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19096·2019-04-02

    Spector & Co. Recalls T119 Elf Power Bank Chargers Due to Fire Hazard

    Spector & Co. is recalling T119 Elf power bank chargers because they can overheat and pose a fire hazard. No injuries or property damage have been reported.

    Product
    T119 Elf power bank chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V268000·2019-04-02

    Spartan Metrostar Emergency Vehicles Recalled for Brake Light Wiring Defect

    Precision Industries is recalling 2017-2018 Spartan Metrostar emergency vehicles because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    SPARTAN — SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19732·2019-04-02

    John Deere Recalls Snow Blower and Broom Attachment Kits for Missing Manuals

    John Deere is recalling about 2,550 snow blower and broom attachment kits because they are missing the Operator's Manual, which poses an injury hazard.

    Product
    Attachment Kits for John Deere Snow Blowers and 52-inch Brooms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V270000·2019-04-02

    Jayco Recalls Motorhomes Due to Missing Blower Motor Fuse

    Jayco is recalling 2014-2019 Precept, 2016-2019 Alante, and 2019 Precept Prestige motorhomes because a missing fuse in the blower motor circuit may cause wiring to overheat and increase fire risk.

    Product
    JAYCO — JAYCO ALANTE, PRECEPT, PRECEPT PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V267000·2019-04-02

    KME Fire Apparatus Recall for Sliding Cover Lock Defect

    KME is recalling specific fire apparatus models because the gas spring lock for the sliding cover may fail to engage, creating an injury risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER, COMMERCIAL PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·040-2019·2019-04-02

    AdvancePierre Recalls Frozen Beef Patties Due to Possible Plastic Contamination

    AdvancePierre Foods is recalling approximately 20,373 pounds of frozen beef patties that may contain soft purple plastic. No illnesses have been reported.

    Product
    AdvancePierre Foods, Inc. — AdvancePierre Foods, Inc. Recalls Frozen Beef Patties due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V260000·2019-04-01

    Labrie CNG Refuse Trucks Recalled for Valve Stem Ejection Risk

    Labrie is recalling 2017-2018 Automizer and Expert CNG refuse trucks because valve stems may forcibly eject, posing injury and fire risks.

    Product
    LABRIE — LABRIE AUTOMIZER, EXPERT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V261000·2019-04-01

    Eldorado Shuttle Bus Recall for Reversed Backup Camera Image

    Eldorado is recalling 2017-2018 shuttle buses because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    ELDORADO — ELDORADO ADVANTAGE, AEROTECH, AERO ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V258000·2019-03-29

    Forest River Recalls 2017-2019 Rockport Work Trucks for Fire Risk

    Forest River is recalling 2017-2019 Rockport work trucks because a missing inline fuse may allow excess current to melt wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide