The Recall Desk

State

Louisiana product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46501–46525 of 80783

  • ModerateFDA (Food)·F-2462-2017·2017-07-19

    3CS Organics Recalls HIPP Bio Combiotik Infant Formula for Labeling Issues

    3CS Organics LLC is recalling HIPP Bio Combiotik infant formula products because they are not FDA approved and not all products are labeled in English.

    Product
    HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Combiotik 2, Canister, 900g (4/case), HIPP Bio Combiotik 3, Canister, 900g (4/case), HIPP Bio Combiotik 1, 600g (4bx/case), HIPP Bio Combiotik 2, 600g (4bx/case), HIPP Bio Combiotik 3, 600g (4/case), HIPP Bio Compiotik…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2467-2017·2017-07-19

    HOLLE Organic Infant Formula Recalled for Lack of FDA Approval

    3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400g (6/case), HOLLE Bio Lait pour Nourrissons Zulgelingenmelk, 400g (6/case), HOLLE Lait Pour Nourrissons 1er Age Bio, 400g (6/case). HOLLE Bio Lait de Suit Au Lait De Chevre, 400g (6/case) , HOLLE…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2730-2017·2017-07-19

    Beckman Coulter Synchron AQUA CAL Level 1 Calibration Kits Recalled

    Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.

    Product
    Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Creatine, Ca, CO2, and P in UniCel DxC Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2383-2017·2017-07-19

    Source Naturals Renewal Antioxidant Tablets Recalled for Undeclared Boron

    Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.

    Product
    Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2461-2017·2017-07-19

    HIPP Anti-Reflux Infant Formula Recalled for Lack of FDA Approval

    3CS ORGANICS LLC is recalling HIPP Anti-Reflux AR Bio-Spezialnahrung because the product is not FDA approved and lacks complete English labeling.

    Product
    HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2715-2017·2017-07-19

    CryoLife On-X Prosthetic Heart Valve Recall for Incorrect Labeling

    CryoLife, Inc. is recalling 52 On-X Prosthetic Heart Valves because the sewing ring type was mislabeled as Standard instead of Anatomic.

    Product
    On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2701-2017·2017-07-19

    Natus Medical Recalls Olympic Pasteurmatic 3000 and 3500 Disinfection Systems

    Natus Medical is recalling Olympic Pasteurmatic 3000 and 3500 systems because they do not fully meet current regulatory requirements due to design age and component obsolescence.

    Product
    The Olympic Pasteurmatic 3000 and Olympic Pasteurmatic 3500 are intended for cleaning and high-level disinfection of respiratory therapy and anesthesia equipment by killing vegetative bacteria and viruses, in a hot water bath at ~160¿ - ~170¿ F for 30 minutes. Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2468-2017·2017-07-19

    3CS Organics Recalls Lebenswert Infant and Toddler Milk Formulas

    3CS Organics LLC is recalling specific Lebenswert infant and toddler milk formulas because the products are not FDA approved and lack full English labeling.

    Product
    Lebenswert Bioland Anfangsmilch1, 500g (4/case), Lebenswert Bioland Folgemilch 2, 500g (4/case), Lebenswert Bioland Folgemilch 3, 475g (5/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2725-2017·2017-07-19

    AMS Diagnostics Recalls Medica ISE Module Calibrant A Due to Physical Defects

    AMS Diagnostics is recalling 9 units of Medica ISE Module Calibrant A because the lot was not functioning properly and did not exhibit correct physical properties.

    Product
    Medica ISE Module Calibrant A; 500 mL - 140 mmol/L Na+, 125 mmol/L Cl-, buffers and preservatives; For use with ISE Module; Product Usage: Calibrations of ISE Model for integrated electrolyte system analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V457000·2017-07-18

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Rupture Risk

    Mazda is recalling specific 2007-2012 CX-7, CX-9, and Mazda6 vehicles because the passenger air bag inflators may rupture in a crash, potentially causing serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, CX-7, CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E038000·2017-07-18

    TriMark Recalls Ambulance Door Striker Bolts for Crash Safety Non-Compliance

    TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17756·2017-07-18

    Polaris Recalls RZR 570 and RZR S 570 Off-Highway Vehicles

    Polaris is recalling about 1,160 RZR 570 and RZR S 570 vehicles because the front brake can detach, posing crash and injury hazards.

    Product
    Polaris RZR 570 and RZR S 570 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V456000·2017-07-18

    Winnebago Recalls 2015 Transit Buses for Weight Rating Compliance Issues

    Winnebago is recalling 2015 Transit Bus 28SH and 28WC models because they may exceed weight ratings when fully loaded, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRANSIT BUS28SH, TRANSIT BUS28WC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V455000·2017-07-18

    Pierce Fire Trucks Recalled for Water Pump Interlock Failure

    Pierce is recalling 2016-2017 fire trucks because a pressure switch may fail in extreme cold, preventing the water pump from operating.

    Product
    PIERCE — PIERCE ENFORCER, VELOCITY, QUANTUM, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V454000·2017-07-17

    Thomas Built Buses Saf-T-Liner C2 Recalled for Wheelchair Anchorage Defect

    Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 transit buses because the wheelchair pocket track anchorage may not secure a wheelchair in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V451000·2017-07-17

    Freightliner Custom Chassis XCR Recalled for Battery Cable Fire Risk

    Daimler Trucks North America is recalling 2014-2017 Freightliner Custom Chassis XCR vehicles because an improperly installed battery cable bracket may cause a short circuit and fire.

    Product
    FCCC — FCCC, FREIGHTLINER CUSTOM CHASS XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V452000·2017-07-17

    Daimler Trucks Recalls 2018 Freightliner and Western Star Models for Tow Hook Defect

    Daimler Trucks North America is recalling 2,483 2018 Freightliner and Western Star trucks because their tow hooks may fail during recovery operations, increasing the risk of injury.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR M2 BUSINESS CLASS, 122SD, CASCADIA, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E037000·2017-07-17

    PACCAR Recalls Braden Hydraulic Recovery Winches Due to Adapter Defect

    PACCAR is recalling specific Braden Hydraulic Recovery winches because a defective ring gear adapter may cause failure under load, posing an injury risk.

    Product
    EQUIPMENT:MECHANICAL:WINCH recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V453000·2017-07-17

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Wheelchair Defect

    Daimler Trucks North America is recalling 2005-2018 Thomas Built Buses Saf-T-Liner C2 school buses because wheelchair pocket track anchorages may not secure wheelchairs in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V448000·2017-07-16

    Smart Fortwo Recall for Parking Brake Cable Lock Nut Issue

    Mercedes-Benz USA is recalling 2016 Smart Fortwo vehicles because the parking brake cable lock nut may loosen, potentially reducing the vehicle's ability to stay secured on slopes.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·082-2017·2017-07-15

    Marathon Enterprises Recalls Hot Dogs Due to Bone Fragment Contamination

    Marathon Enterprises is recalling approximately 7.2 million pounds of hot dog products due to potential bone fragment contamination. One minor oral injury has been reported.

    Product
    Marathon Enterprises Inc. — Marathon Enterprises Inc. Recalls Hot Dog Products Due to Possible Extranous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V447000·2017-07-14

    Mercedes-Benz Recalls 2017 Smart Fortwo Vehicles for Steering Knuckle Defect

    Mercedes-Benz USA is recalling 2017 Smart Fortwo and Cabriolet vehicles because casting imperfections in the left front axle steering knuckle could cause failure and increase crash risk.

    Product
    SMART — SMART FORTWO, FORTWO CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide