The Recall Desk

State

Louisiana product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48976–49000 of 80793

  • ModerateFDA (Devices)·Z-1204-2017·2017-02-22

    Siemens CentraLink Software Recalled for Potential Sample Type Omission

    Siemens is recalling CentraLink Data Management System software versions v13x, v14x, and v15x because the system may download orders to the ADVIA Automation System without specifying the sample type.

    Product
    CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1189-2017·2017-02-22

    BD Vacutainer Blood Collection Tubes Recalled for Excess Anticoagulant

    Becton Dickinson is recalling specific lots of BD Vacutainer blood collection tubes because they contain approximately twice the expected amount of buffered sodium citrate additive.

    Product
    BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5 ml x 13 x 75 mm) Catalog Number: 369714 Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection tube that provides means of collecting, transporting and processing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0479-2017·2017-02-22

    Teva Recalls Mimvey Lo Tablets Due to Impurity Test Failures

    Teva Pharmaceuticals USA is recalling specific lots of Mimvey Lo tablets because they failed impurity specifications for norethindrone.

    Product
    Mimvey Lo (estradiol and norethindrone acetate tablets USP), 0.5 mg/0.1 mg, 28 tablets per blister card (NDC 0093-5454-18), packaged in 3 blister cards per carton (NDC 0093-5454-62), Rx only, Manufactured By: Barr Laboratories, Inc., Pomona, NY 10970; Manufactured For: Teva…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1190-2017·2017-02-22

    Greatbatch Recalls T5766 Offset Reamer Handles Due to Drive Chain Seizure

    Greatbatch Medical is recalling 1,441 T5766 Offset Reamer Handles because the drive chain U-joints may seize during hip surgery, rendering the device non-functional.

    Product
    Offset Reamer Handle, T5766 Product Usage: The reamer handles are re-usable surgical instruments used in arthroplasty surgery of the hip joints, where either total joint replacement or resurfacing surgery is performed using a reamer cutting instrument. The reamer handles are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1221-2017·2017-02-22

    Atrium Medical Recalls 8 Fr Thoracic Catheters Due to Labeling Error

    Atrium Medical Corporation is recalling 8 Fr Straight Thoracic Catheters because the label depicts six eyelets instead of the correct two.

    Product
    Atrium PVC 8 Fr Straight Thoracic Catheter Code Number: 8008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0478-2017·2017-02-22

    Accord Healthcare Recalls Lisinopril Tablets Due to Missing Break Line

    Accord Healthcare is recalling 12,896 bottles of 5 mg Lisinopril tablets because the tablets are missing a break line. The recall covers the U.S. and Puerto Rico.

    Product
    Lisinopril tablets, 5 mg, 1000-count bottle, Rx only, Manufactured for Accord Healthcare, Inc., Durham, NC 27703, NDC 16729-376-17
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1196-2017·2017-02-22

    Argon Medical Devices Recalls Harvest Needles Due to Sterility Concerns

    Argon Medical Devices is recalling 15 boxes of Harvest Needles because a potential defect in the blister packaging may compromise the sterility of the product.

    Product
    HARVEST NEEDLE 15GA X 2 Intended for the purpose of harvesting bone and/or bone marrow specimens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0477-2017·2017-02-22

    Taclonex Topical Suspension Recalled for Outdated Package Insert

    LEO Pharma Inc. is recalling Taclonex topical suspension because it was packaged with an out-of-date package insert.

    Product
    TACLONEX — TACLONEX (CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1484-2017·2017-02-22

    NOW Foods Recalls Multi-Food 1 Tablets Due to Labeling Error

    NOW Foods is recalling Multi-Food 1 Tablets because the label incorrectly states the molybdenum content is 75 mg instead of 75 mcg.

    Product
    NOW¿ Multi-Food 1 Tablets, One Tablet Daily, 90 tablets, A Dietary Supplement
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V111000·2017-02-21

    Yamaha Recalls 2015-2016 YZF-R3 Motorcycles for Fuel Tank Leak Risk

    Yamaha is recalling 2015-2016 YZF-R3 motorcycles because engine vibration may cause the fuel tank bracket to contact the tank, potentially leading to a fuel leak and fire risk.

    Product
    YAMAHA — YAMAHA redundant YZF-R3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E012000·2017-02-21

    LiquidSpring Recalls Suspension Systems Due to Brake Bolt Tightening Defect

    LiquidSpring is recalling certain Compressible Liquid Adaptive Suspension Systems because overtightened rear brake banjo bolts may cause loss of rear brakes, increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17090·2017-02-21

    Yamaha Recalls Grand Piano Benches Due to Lead Paint Violation

    Yamaha Corporation of America is recalling about 900 piano benches sold with grand pianos because the interior paint contains excessive lead, violating federal standards.

    Product
    Piano benches sold with Yamaha grand piano
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V108000·2017-02-20

    Winnebago Recalls 2016-2017 Travato RVs Due to Propane Hose Hazard

    Winnebago is recalling 2016-2017 Travato recreational vehicles because the liquid propane hose may contact the emergency brake cable, potentially causing a propane leak that increases the risk of fire or explosion.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E010000·2017-02-20

    Autoliv Recalls AI2 Air Bag Initiators Due to Deployment Failure Risk

    Autoliv is recalling AI2 Air Bag Initiators manufactured between June 2016 and November 2016 because an improper chemical mix may prevent air bags from deploying properly in a crash.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E011000·2017-02-20

    Roush Propane Conversion Kits Recalled for Potential Fuel Leak

    Roush CleanTech is recalling propane conversion kits for Ford F-250 trucks because worn fittings may cause a propane leak, increasing fire risk.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V107000·2017-02-17

    Altec Recalls 2016 Digger Derrick Vehicles Due to Fastener Failure Risk

    Altec Industries is recalling 2016 DLB Digger Derrick vehicles because fasteners securing the outer rotation bearings may fail, potentially causing the boom to move unintentionally.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V105000·2017-02-17

    Isuzu Recalls 2015-2017 Trucks Due to Frame Crossmember Burrs

    Isuzu is recalling 2015-2017 NPR HD, NPR XD, NQR, and NRR trucks because burrs on the frame crossmember may cause transmission mounting studs to break, increasing crash risk.

    Product
    ISUZU — ISUZU NRR, NQR, NPR XD, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V106000·2017-02-17

    Keystone Recalls 2017 Dutchmen Coleman Trailers for Incorrect Tire Labeling

    Keystone is recalling 2017 Dutchmen Coleman recreational trailers because the Federal Identification Tag lists incorrect tire and rim sizes, which could lead to improper equipment use.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17088·2017-02-16

    Britax Recalls Strollers Due to Car Seat Fall Hazard

    Britax is recalling B-Agile and BOB Motion strollers because a damaged receiver mount can cause car seats to fall, posing a hazard to infants.

    Product
    Britax B-Agile and BOB Motion Strollers with Click & Go receivers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17E009000·2017-02-16

    Hale Fire Pump Pressure Switch Recall for Cold Weather Failure

    Hale Products Inc. is recalling Fire Pump Engagement Pressure Switches that may fail in extremely cold temperatures, potentially delaying water delivery during fires.

    Product
    EQUIPMENT:MECHANICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V104000·2017-02-16

    Volvo Recalls 2017 Models Due to Air Bag Bolt Failure Risk

    Volvo is recalling 2017 XC90, S90, and V90 Cross Country vehicles because side air bag bolts may break, causing improper deployment in a crash.

    Product
    VOLVO — VOLVO V90CC, S90, XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide