The Recall Desk

State

Louisiana product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44801–44825 of 80775

  • ModerateFDA (Devices)·Z-0041-2018·2017-11-01

    Encore Medical Recalls EMPOWR PS Knee Inserts Due to Packaging Error

    Encore Medical is recalling 48 units of EMPOWR PS Knee inserts because one unit was packaged with the wrong implant reference number.

    Product
    EMPOWR PS KNEE(TM) e+, REF 343-13-708, SIZE 8, 13mm, QTY 01, SKY BLUE, STERILE Product Usage The EMPOWR PS Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0047-2018·2017-11-01

    Siemens Medical Solutions Recalls Torque Wrenches for Symbia CT Devices

    Siemens Medical Solutions is recalling 16 torque wrenches used to install Symbia CT scanners because the tools were found to be out of tolerance.

    Product
    Torque wrench used on the bolts for the Symbia T2 model 10275008, Symbia Intevo Excel model 10764801, Symbia Intevo 16 model 10764804, Symbia Evo model 10910500, and Symbia Evo Excel model 10910501 devices.
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Drugs)·D-0051-2018·2017-11-01

    Wockhardt Recalls Enalapril Maleate Tablets Due to Impurity Failures

    Wockhardt USA is recalling 5mg Enalapril Maleate tablets because they failed impurity specifications. The recall covers 5,050 bottles distributed nationwide.

    Product
    Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India, Distributed by: Wockhardt, USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054, USA. NDC: 64679-924-03;
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0052-2018·2017-11-01

    Teva Recalls Methylphenidate Hydrochloride Tablets Due to Dissolution Failures

    Teva Pharmaceuticals USA is recalling 58,292 bottles of Methylphenidate Hydrochloride Tablets USP, 20 mg, because they failed to meet dissolution specifications.

    Product
    Methylphenidate Hydrochloride Tablets USP, 20 mg, 100-count bottles, Rx only, Manufactured by: Watson Laboratories, Inc., Corona, CA 92880 USA, NDC 0591-5884-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0073-2018·2017-11-01

    Vi-Jon Recalls Equate and Studio 35 Face Moisturizers for Stability Failures

    Vi-Jon, Inc. is recalling Equate and Studio 35 Clarifying Face Daily Moisturizers because the products failed stability specifications. The recall covers 67,532 bottles distributed nationwide.

    Product
    Equate Beauty Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed by: Wal-Mart Stores, Inc. Bentonville, AR 72716, NDC # 4903594126 UPC # 681131150774. Studio 35 Beauty Daily Clarifying Face Daily Moisturizer 4 fl. oz. (118 mL) Distributed By: Walgreen Co. 200…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0146-2018·2017-11-01

    Taro Recalls Fluocinonide Gel Due to Dapsone Cross-Contamination

    Taro Pharmaceuticals is recalling 16,944 tubes of Fluocinonide Gel USP 0.05% because traces of Dapsone were found in the finished product.

    Product
    FLUOCINONIDE — FLUOCINONIDE (FLUOCINONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V686000·2017-10-30

    Mitsubishi Mirage Recall: Air Bags May Fail to Deploy in Crash

    Mitsubishi is recalling 2014-2018 Mirage vehicles because the air bag system may disable itself due to sensor errors, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V683000·2017-10-30

    BMW Recalls 740,561 Vehicles for PCV Valve Fire Risk

    BMW is recalling 740,561 vehicles from 2007-2011 because a short circuit in the PCV valve heater can cause a fire.

    Product
    BMW — BMW 328I, 128I, X5, 530I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18018·2017-10-30

    Polaris Recalls General Off-Highway Vehicles Due to Steering Shaft Hazard

    Polaris is recalling about 19,000 General side-by-side vehicles because the steering wheel shaft can shift and detach, creating a crash risk.

    Product
    Polaris General side-by-side recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V687000·2017-10-30

    MCI Recalls 2018 J4500 Buses Due to Incorrect Air Line Connections

    Motor Coach Industries is recalling 2018 MCI J4500 buses because air lines were incorrectly hooked to pressure gauges, potentially delaying driver response to low air conditions.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V685000·2017-10-27

    Eldorado Buses Recalled for Stuck Seat Belt Buckles

    Eldorado is recalling 2017 Axess, Arrivo, XHF, and E-Z Rider II buses because seat belt buckles may be stuck, preventing use.

    Product
    ELDORADO — ELDORADO AXESS, ARRIVO, XHF, E-Z RIDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V682000·2017-10-27

    Indian Recalls 2017-2018 Motorcycles for Non-Compliant Headlight Assemblies

    Indian Motorcycle is recalling 2,096 models from 2017-2018 because some may have European-market headlights that fail US safety standards, increasing crash risk.

    Product
    INDIAN — INDIAN CHIEFTAIN DARK HORSE, CHIEFTAIN, CHIEF VINTAGE, SPRINGFIELD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V680000·2017-10-26

    Tremcar Recalls Hutchinson and Tremcar Trailers Due to Weak Rear Impact Guards

    Tremcar is recalling specific Hutchinson and Tremcar trailers because their rear impact guards were made with insufficiently strong aluminum alloy.

    Product
    HUTCHINSON — HUTCHINSON, TREMCAR 406 2 AXLE SEMI-TRAILER, 406 B-TRAIN PUP, 406 QUAD WAGON, 406 3 AXLE SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V677000·2017-10-26

    Forest River Recalls 2017-2018 Rockwood and Flagstaff Travel Trailers

    Forest River is recalling 2017-2018 Rockwood and Flagstaff travel trailers because the slide room arm may damage the rear tire, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V681000·2017-10-26

    Honda Recalls 2017 CBR1000RR Motorcycles Due to Fuel Tank Water Ingress Risk

    Honda is recalling 2,443 2017 CBR1000RR and CBR1000RR SP motorcycles because a gap in the fuel tank cap seal may allow water to enter the tank, potentially causing engine stalling and increasing crash risk.

    Product
    HONDA — HONDA CBR1000RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V679000·2017-10-26

    Land Rover Recalls 2017 Range Rover Models for Instrument Cluster Defect

    Jaguar Land Rover is recalling 2017 Range Rover and Range Rover Sport vehicles because the instrument cluster may intermittently go blank, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0012-2018·2017-10-25

    RXQ Compounding Recalls Methylprednisolone Acetate Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling 945 vials of methylprednisolone acetate injection because autoclave parameters were incorrect, raising concerns about product sterility.

    Product
    methylPREDNIsolone ACETATE, 40 MG/ML INJECTION SUSPENSION, 10 ML Vial, RXQ Compounding, Athens, OH --- NDC: 70731-0936-10
    Category
    Drug
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0013-2018·2017-10-25

    Alprazolam Tablets Recalled for Unknown Impurity

    The Harvard Drug Group is recalling Alprazolam Tablets, 0.25 mg, due to an out-of-specification result for an unknown impurity.

    Product
    Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V676000·2017-10-25

    BMW Recalls 2006-2011 3 Series Vehicles for Fire Risk

    BMW is recalling 2006-2011 3 Series vehicles because heating and air conditioning wiring may overheat, increasing the risk of a fire.

    Product
    BMW — BMW 325XI, 323I, 325I, 328I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0028-2018·2017-10-25

    Death Wish Nitro Canned Cold Brew Coffee Recalled for Botulism Risk

    Death Wish Coffee Company is recalling 80,777 cans of Nitro Canned Cold Brew Coffee nationwide due to a potential for Clostridium Botulinum.

    Product
    Death Wish Nitro Canned Cold Brew Coffee 11 oz UPC: 851552005599
    Category
    Food
    Distribution
    Distributed nationwide