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.

Which agencies issued them

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.

31651–31675 of 80702

  • ModerateFDA (Devices)·Z-1971-2020·2020-05-20

    BD Biosciences Recalls CD45 Reagent Due to False Positive Reactions

    Becton, Dickinson and Company is recalling 1,473 vials of Analyte specific reagent (CD45) because of false positive reactions. The product is used for in vitro diagnostic testing.

    Product
    Analyte specific reagent. REF/UDI: 641408/641408-4012-1-1 (US); 641417/641417-1157-1-01 (OUS); 641399/641399-4012-1-01 (US Research Use Only) - Product Usage: CD45 is intended for in vitro diagnostic use in the identification of cells expressing the CD45 antigen, using a BD FAC…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2006-2020·2020-05-20

    Ra Medical Systems Recalls DABRA Catheters Due to Calibration Failure Risk

    Ra Medical Systems is recalling DABRA catheters because the actual shelf life is shorter than labeled, potentially causing calibration failures.

    Product
    Ra Medical Systems DABRA Catheter 5F (1.5mm), REF: 1222-5000-01, LOT: 18-090400-094, USE BY: 2019-09-24, MFR DATE: 2018-09-24, CE, Laser Radiation, STERILE (Gamma Sterilized), Single Use Only Revised Label: Product Label - Ra Medical Systems DABRA Catheter 5F (1.5mm)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1930-2020·2020-05-20

    Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions

    Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.

    Product
    VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 805 8232-300 slides, UDI Number 10758750004294 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2005-2020·2020-05-20

    Genicon EZee Specimen Retrieval Bag Recall for Labeling Clarity

    Genicon is recalling 1,550 units of the EZee Single Use Specimen Retrieval Bag to provide updated labeling instructions for multiple specimen retrieval.

    Product
    Genicon EZee Single Use Specimen Retrieval Bag - Product Usage: This device is disposable and is packaged and sterilized for single use only. The bag may be used for multiple specimen retraction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1949-2020·2020-05-20

    Cardiac Assist Recalls TandemHeart Kits Due to Assembly Error

    Cardiac Assist, Inc. is recalling five TandemHeart pump kits because an assembly error may prevent the device from priming.

    Product
    TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15, Product: 5710-6215 - Product Usage: provides temporary extracorporeal circulatory system support with the unique ability to locally deliver an anticoagulant through the infusion system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1931-2020·2020-05-20

    Ortho-Clinical Diagnostics Recalls VITROS CKMB Slides Due to Incorrect Instructions

    Ortho-Clinical Diagnostics is recalling VITROS CKMB Slides because Spanish and Swedish instructions incorrectly state the assay can be tested with plasma, which could result in biased results.

    Product
    VITROS Chemistry Products CKMB Slides, Creatine Kinase MB, Product Code 8001133-90 slides, UDI Number 10758750004201 - Product Usage: The VITROS Chemistry Product Slides are used to measure creatine kinase MB (CK-MB) activity in serum which used to be ordered to detect…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1941-2020·2020-05-20

    Medtronic Recalls Vertex Select Multi Axial Screws Due to Length Discrepancy

    Medtronic is recalling 83 Vertex Select Multi Axial Screws because the product length is shorter than labeled. The recall covers units distributed in California and Michigan.

    Product
    VERTEX SELECT MULTI AXIAL SCREW. 4.0 X 38MM MULTI AXIAL SCREW. Lot H5517628
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1946-2020·2020-05-20

    Becton Dickinson Recalls PowerGlide ST Midline Catheter Kits Missing Lidocaine

    Becton Dickinson is recalling 655 PowerGlide ST Midline Catheter Maximal Barrier Kits because they were packaged without the required lidocaine.

    Product
    PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D
    Category
    Medical Device
    Distribution
    14 states
  • LowFDA (Drugs)·D-1267-2020·2020-05-20

    ChapStick Total Hydration Moisture Tint Recalled for Packaging Separation

    Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Very Berry due to observed separation in the secondary packaging.

    Product
    CHAPSTICK TOTAL HYDRATION MOISTURE TINT VERY BERRY — CHAPSTICK TOTAL HYDRATION MOISTURE TINT VERY BERRY (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1268-2020·2020-05-20

    ChapStick Total Hydration Moisture Tint Recalled for Packaging Separation

    Glaxosmithkline is recalling ChapStick Total Hydration Moisture Tint Pretty in Pink due to observed separation in the secondary packaging.

    Product
    CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK — CHAPSTICK TOTAL HYDRATION MOISTURE TINT PRETTY IN PINK (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1266-2020·2020-05-20

    ChapStick Lip Balm Recalled for Packaging Separation

    Glaxosmithkline is recalling 288 packages of ChapStick Total Hydration Moisture Tint Peachy Keen due to observed separation in the secondary packaging.

    Product
    CHAPSTICK TOTAL HYDRATION MOISTURE TINT PEACHY KEEN — CHAPSTICK TOTAL HYDRATION MOISTURE TINT PEACHY KEEN (ZINC OXIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V282000·2020-05-19

    Altec Recalls Aerial Devices and Digger Derricks Due to Bolt Failure Risk

    Altec is recalling 2018-2020 aerial devices and digger derricks because bolts securing the pedestal to the turntable may fail, increasing the risk of injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V279000·2020-05-18

    Mitsubishi Recalls Lancer and Outlander Models for Corroded Front Cross Members

    Mitsubishi is recalling specific Lancer, Outlander, and Outlander Sport vehicles because front cross members may corrode and detach, increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI LANCER, OUTLANDER, OUTLANDER SPORT, LANCER SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V281000·2020-05-18

    Western Star 4700 and 5700 trucks recalled for ground harness wiring defect

    DTNA is recalling certain 2019-2021 Western Star 4700 and 5700 trucks. An undersized wire in the ground harness may cause a melted connector, leading to engine stall and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR 4700, 5700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V280000·2020-05-18

    Mitsubishi Recalls Outlander Models Due to Second-Row Seat Belt Assembly Defect

    Mitsubishi is recalling 2019-2020 Outlander and 2019 Outlander PHEV vehicles because the right-side second-row seat belt may be assembled incorrectly, potentially failing to restrain occupants in a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V277000·2020-05-15

    Yamaha Recalls 2015-2018 XC155 Scooters Due to Cylinder Head Nut Issue

    Yamaha is recalling 2015-2018 XC155 scooters because cylinder head nuts may loosen, causing coolant to foul the spark plug and potentially leading to engine stalling.

    Product
    YAMAHA — YAMAHA SMAX, XC155F
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20122·2020-05-14

    Garia Recalls Electric Golf and Courtesy Vehicles Due to Fire Hazard

    Garia is recalling about 1,000 battery-powered golf and courtesy vehicles because a fuse can overheat and melt while charging, posing a fire hazard.

    Product
    Garia Golf & Courtesy battery-powered electric vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20744·2020-05-14

    John Deere Recalls Broom Attachment Kits Due to Missing Manual

    John Deere is recalling 60-inch broom attachment kits for compact utility tractors because they lack the required Operator's Manual, posing an injury hazard.

    Product
    Attachment Kits for John Deere 60-inch Brooms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20743·2020-05-14

    Jade Bloom Essential Oils Recalled for Non-Child-Resistant Packaging

    W8 Distributing is recalling Jade Bloom Wintergreen and Birch Sweet Essential Oils because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Jade Bloom Wintergreen and Birch Sweet Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V275000·2020-05-14

    Heartland Recalls 2020 Trailers Due to Spare Tire Carrier Defect

    Heartland is recalling 2020 Trail Runner, Wilderness, Mallard, and Prowler trailers because a U-bolt on the spare tire carrier may break, causing the tire to detach.

    Product
    HEARTLAND — HEARTLAND TRAIL RUNNER, WILDERNESS, MALLARD, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20745·2020-05-14

    Organic Pure Oil Recalls Wintergreen Essential Oil for Packaging Defect

    Organic Pure Oil is recalling Wintergreen Essential Oil because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Organic Pure Oil Wintergreen Essential Oil
    Category
    Consumer Product
    Distribution
    Distributed nationwide