The Recall Desk

State

Louisiana product recalls

73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,967
Critical
1,107
Severe
1,740
Most recent
2026-11-14

Of the 6,967 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 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52126–52150 of 80800

  • ModerateFDA (Devices)·Z-2369-2016·2016-08-17

    Philips Brilliance 16 CT Systems Recalled for Software Defect

    Philips Medical Systems is recalling 203 Brilliance 16 CT systems due to a software defect causing intermittently slow response of the Host.

    Product
    Brilliance 16 Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    46 states
  • ModerateFDA (Devices)·Z-2370-2016·2016-08-17

    Philips Brilliance CT 16 Power Systems Recalled for Software Defect

    Philips Medical Systems is recalling 55 Brilliance CT 16 Power systems due to a software defect causing intermittently slow response of the Host.

    Product
    Brilliance CT 16 Power Computed Tomography X-ray systems is intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    46 states
  • LowFDA (Devices)·Z-2378-2016·2016-08-17

    BD Tritest CD3/CD4/CD45 Reagent Recalled for Incorrect Labeling

    Becton, Dickinson and Company is recalling 14,089 vials of BD Tritest CD3 FITC/CD4 PE/CD45 PerCP because the label incorrectly states the product contains gelatin.

    Product
    BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP with Gelatin and 0.1% sodium azide. Hematology: BD Tritest CD3 fluorescein isothiocyanate (FITC)/CD4 phycoerythrin (PE)/CD45 peridinin chlorophyll…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V606000·2016-08-16

    KME Predator Emergency Vehicles Recalled for Front Grille Separation Risk

    Kovatch Mobile Equipment is recalling 27 KME Predator emergency vehicles from 2012-2013 because the front grille may loosen and separate from the cab, creating a road hazard.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR PANTHER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V603000·2016-08-16

    Mercedes-Benz Recalls 2016 C300 and GLC300 for Electronic Stability Control Defect

    Mercedes-Benz is recalling 2016 C300 and GLC300 vehicles because a damaged Electronic Stability Program control unit may activate stability control or disable the parking brake, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V599000·2016-08-15

    Autocar Recalls 2016-2017 Xspotter Vehicles for Steering Column Defect

    Autocar is recalling 294 model year 2016-2017 Xspotter vehicles because a steering column shaft weld may break, causing a loss of steering ability and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V601000·2016-08-15

    Spartan Motors Recalls 2014-2016 Legend and Star Fire Trucks

    Spartan Motors is recalling 2014-2016 Legend and Star fire trucks due to a transmission defect that may prevent power output switching, risking injury.

    Product
    SPARTAN ERV — SPARTAN ERV LEGEND, STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V600000·2016-08-15

    Keystone Recalls 2011-2017 Bullet and Passport Trailers for Fire Risk

    Keystone is recalling 2011-2017 Bullet and Passport recreational trailers because an improperly wired air conditioner thermostat may cause an electrical short and fire.

    Product
    KEYSTONE — KEYSTONE BULLET, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V602000·2016-08-15

    Mercedes-Benz Recalls 2016 GLE450 for Rear Head Restraint Defect

    Mercedes-Benz is recalling 2016 GLE450 vehicles because rear head restraints may not stay locked in very low temperatures, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V596000·2016-08-12

    Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect

    Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because improperly tightened rear suspension arms may fail, causing loss of vehicle control.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4, HS 250 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V597000·2016-08-12

    Harbor Freight Recalls Haul Master Trailers for Rear Lamp Bracket Defect

    Harbor Freight is recalling 2006-2016 Haul Master trailers because incorrectly positioned rear lamp brackets may fail to illuminate the license plate, increasing crash risk.

    Product
    HAUL MASTER — HAUL MASTER TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V598000·2016-08-12

    Winnebago Recalls 2015-2017 Recreational Vehicles Due to Electrical Fire Risk

    Winnebago is recalling 2015-2017 Itasca and Winnebago recreational vehicles because a loose electrical connection may cause heat buildup and increase the risk of a fire.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA FUSE, CAMBRIA, ASPECT, TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16T011000·2016-08-12

    Goodyear Recalls Dunlop SP50 Tires Due to Tread Chunking Risk

    Goodyear is recalling specific Dunlop SP50 tires manufactured between December 2012 and February 2014 because they may experience tread chunking, which increases the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V593000·2016-08-11

    Mazda Recalls CX-7 Vehicles Due to Front Suspension Corrosion Risk

    Mazda is recalling 2007-2012 CX-7 vehicles because water and salt may cause front suspension ball joints to corrode and separate, potentially leading to a loss of steering control.

    Product
    MAZDA — MAZDA CX-7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V595000·2016-08-11

    GM Recalls 2016 Buick Verano Vehicles Due to Fuel Line Fire Risk

    General Motors is recalling 2016 Buick Verano vehicles because a misrouted fuel line may contact the engine, wear, and leak fuel, increasing the risk of a fire.

    Product
    BUICK — BUICK VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1853-2016·2016-08-10

    ACH Food Companies Recalls Salad Toppings for Listeria Risk

    ACH Food Companies is recalling Durkee, Hy-Vee, and Food Club salad toppings because an ingredient may be contaminated with Listeria monocytogenes.

    Product
    Salad topping labeled under the following brand names: (Product 1) Durkee Salad Topping in plastic bottle, Net Wt. 6.75 oz (192 g), packed in cases of 12. UPC 047600091366. The responsible firm name on the label is ACH Food Companies, Inc. Memphis, TN; (Product 2) Hy-Vee…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V592000·2016-08-10

    Tadano Recalls 2013-2015 All-Terrain Cranes Due to Air Line Defect

    Tadano is recalling 2013-2015 all-terrain crane trucks because an improperly assembled air line connection may cause reduced braking or loss of mobility.

    Product
    TADANO — TADANO ATF70G-4, ATF220G-5, ATF130G-5, ATF400G-6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2339-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 90 units of Air Dermatome II Width Plates because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2215-2016·2016-08-10

    Draeger Recalls Oxylog 3000 Pediatric Patient Circuits Due to Leakage

    Draeger Medical is recalling Oxylog 3000 disposable pediatric patient circuits because isolated episodes of leakage were found at the check valve.

    Product
    Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing circuit is used with the Dr¿ger Oxylog 3000 and Oxylog 3000 plus Emergency Transport Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1871-2016·2016-08-10

    Honey Bunchies Gourmet Honey Bars Recalled for Listeria Risk

    Honey Bunchie, LLC is voluntarily recalling Honey Bunchies Gourmet Honey Bars due to potential Listeria monocytogenes contamination in sunflower kernels.

    Product
    Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar containing honey, sunflower kernels, peanuts and pecans. Packaging: Box containing 20 individual bars in plastic wrappers. Manufactured by: Honey Bunchie, LLC, Longmont, CO. Individual Bar UPC 8 66192 00010 1; Box of 20 Bars…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2255-2016·2016-08-10

    Olympus Analytical X-Ray Systems Recalled for Trigger Lock Failure

    Olympus Scientific Solutions Americas is recalling Analytical X-Ray Systems because the trigger lock may fail to prevent x-ray generation in test modes.

    Product
    Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical X-Ray System X -Ray Fluorescence. Intended to emit ionizing radiation Delta with models: DC-2000, DC-4000, DC-6000, DI-2000, DP-2000, DP-4000, DP-4050, DP- 6000, DPO-4000, DPO-6000, DS-2000…
    Category
    Medical Device
    Distribution
    Distributed nationwide