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.

33776–33800 of 80702

  • SevereNHTSA·19V866000·2019-12-06

    Volkswagen Recalls 2013-2015 Jetta Hybrid for Transmission Defect

    Volkswagen is recalling 2013-2015 Jetta Hybrid vehicles because hairline cracks in the transmission can cause oil leaks and sudden loss of drive power, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20035·2019-12-06

    Trek Recalls Super Commuter+ Electric Bicycles Due to Fall Hazard

    Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.

    Product
    Trek Super Commuter+ 8S
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V869000·2019-12-06

    Daimler Recalls 2020-2021 Thomas Built Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V867000·2019-12-06

    Mercedes-Benz Recalls 2020 GLE 450 for Third-Row Headrest Defect

    Mercedes-Benz is recalling one 2020 GLE 450 4MATIC because third-row headrests may not hold in place, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V868000·2019-12-06

    Mercedes-Benz Recalls 2019 AMG E-Class Models for Air Bag Defect

    Mercedes-Benz is recalling 2019 AMG E53, E63, and E63S models because incorrect driver air bags and software may be installed, increasing injury risk in crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, E63, AMG E53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V865000·2019-12-05

    Honda Recalls 2019-2020 CR-V for Rear Subframe Bolt Defect

    Honda is recalling 2019-2020 CR-V vehicles because improperly manufactured rear subframe bolts may loosen, allowing the subframe to separate and increasing crash risk.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20711·2019-12-05

    DaVinci Bailey Bassinets Recalled Due to Support Leg Breakage Hazard

    DaVinci is recalling about 3,000 Bailey bassinets because support legs can break, posing a fall hazard to infants. Consumers should stop using them and contact the company for a repair kit.

    Product
    DaVinci Bailey bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0196-2020·2019-12-04

    North Bay Produce Apples Recalled for Listeria Contamination Risk

    North Bay Produce is recalling various apple varieties due to potential Listeria monocytogenes contamination. The affected apples were distributed to wholesalers and retailers in eight states.

    Product
    North Bay Produce brand McIntosh, Honeycrisp, Jonathan, Fuji, Jonamac and Red Delicious apples sold in 2 lbs and 3 lbs plastic bags, white paper quarter peck bags, half peck clear plastic tote bags, 600lb bulk, and individually from retailers display trays.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0528-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 300 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Capsules 300 mg, 30-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-145-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0523-2020·2019-12-04

    New Vitalis Pharmacy Recalls Testosterone Injection Due to Sterility Concerns

    New Vitalis Pharmacy is recalling Testosterone Cypionate and Propionate oil injection solutions due to a lack of sterility assurance.

    Product
    Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0525-2020·2019-12-04

    AVKARE Recalls Ranitidine Tablets Due to NDMA Impurity

    AVKARE Inc. is recalling specific lots of Ranitidine Tablets 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    AVKARE Ranitidine Tablets, USP 300 mg Rx Only NDC Manufactured for: AvKARE, Inc. Pulaski, TN 38478 a) 250 tablets NDC 42291-725-25; b) 30 tablets NDC 42291-725-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0524-2020·2019-12-04

    AVKARE Recalls Ranitidine Tablets Due to NDMA Impurity

    AVKARE Inc. is recalling specific lots of Ranitidine Tablets 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    AVKARE Ranitidine Tablets, USP 150 mg Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 Manufactured by: Amneal Pharmaceuticals of NY Hauppauge, NY 11788 a) 1000 tablets NDC 42291-724-10; b) 180 tablets NDC 42291-724-18; c) 60 tablets NDC 42291-724-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0526-2020·2019-12-04

    AuroMedics Recalls Ranitidine Tablets Due to NDMA Detection

    AuroMedics Pharma LLC is recalling DG Health Acid Reducer Ranitidine Tablets 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0529-2020·2019-12-04

    AuroMedics Recalls Ranitidine Syrup Due to NDMA Contamination

    AuroMedics Pharma LLC is recalling Ranitidine Syrup because N-nitrosodimethylamine (NDMA) has been detected in the product.

    Product
    Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5mL) 474 mL bottle, Rx only Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India NDC 65862-431-74
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0573-2020·2019-12-04

    AuroMedics Recalls MARLIDO KIT Vials Due to Foreign Material Presence

    AuroMedics Pharma LLC is recalling MARLIDO KIT vials because foreign material was found inside the vials. The affected product is Lidocaine HCl Injection, USP, 2%.

    Product
    MARLIDO KIT — MARLIDO KIT (MARCAINE, LIDOCAINE, POVIDONE IODINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V860000·2019-12-04

    REV Recalls Fleetwood and Holiday Rambler Motorhomes Due to Exhaust Defect

    REV Recreation Group is recalling 3,241 Fleetwood and Holiday Rambler motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER BOUNDER, SOUTHWIND, VACATIONER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0521-2020·2019-12-04

    Zimmer Biomet Recalls Acromium Flange Sets Due to Cleaning Issues

    Zimmer Biomet is recalling Acromium Flange Sets because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.

    Product
    ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0530-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V859000·2019-12-04

    Ford Recalls 2020 Explorer and Lincoln Aviator for Fuel Leak Risk

    Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a chafing fuel line may cause a leak, increasing the risk of fire.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0527-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Caspules 150 mg, 60-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V862000·2019-12-04

    Volkswagen Recalls Diesel Vehicles for Air Bag Inflator Defect

    Volkswagen is recalling certain 2011-2015 Golf, Passat, and Audi A3 diesel vehicles because the driver's side air bag inflator may explode.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, A3, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0536-2020·2019-12-04

    Helena Laboratories Recalls Platelet Aggregation Kits Due to Contamination

    Helena Laboratories is recalling Platelet Aggregation Kits because the Collagen Reagent vials may contain particulate matter or microbial growth.

    Product
    Platelet Aggregation Kit, Cat. No.5369, For use in platelet aggregation studies, Contains: 2X1 mL ADP Reagent containing adenosine diphosphate, 2X 1 mL Collagen Reagent containing collagen (equine tendon), 2 x 1 mL Epinephrine Reagent containing L-epinephrine, FOR IN-VITRO…
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-0517-2020·2019-12-04

    Zimmer Biomet Recalls 73 Calcar Trimmer Shafts for Mating Failure

    Zimmer Biomet is recalling 73 units of the ASI 2.0 Calcar Trimmer Shaft because the shaft end may fail to mate effectively with the broach.

    Product
    ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
    Category
    Medical Device
    Distribution
    11 states