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.

44651–44675 of 80775

  • HighFDA (Devices)·Z-0075-2018·2017-11-15

    Terumo BCT Recalls Harvest Graft Delivery Packs Due to Seal Defect

    Terumo BCT is recalling 525 Harvest Graft Delivery Packs because some lots may lack a seal on the inner pouch, potentially compromising sterility.

    Product
    HARVEST TERUMOBCT, GCP-10 Graft Delivery Pack, REF 51449, Rx Only, STERILE EO Harvest Graph Delivery System is a disposable pack that takes the cell concentrate created while using the BMAC Procedure Packs and allows for hydration of bone graft material for application to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0076-2018·2017-11-15

    Sorin FlexFlow Venous Cannula Recalled for Sharpness Defect

    Sorin Group USA is recalling a specific lot of FlexFlow Venous Cannulas because they are sharper or pointier than expected.

    Product
    FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is a size 23 French with an outside diameter of 0.30 inch (7.7 mm) and an effective working length of 11.2 inch (28.5 cm). The FlexFlow Venous Cannula is an open…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2018·2017-11-15

    Encore Medical Recalls Cobalt MV Bone Cement Due to Packaging Seal Loss

    Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0087-2018·2017-11-15

    Epimed RX-2 COUDE Epidural Needle Recalled for Potential Sterility Seal Defect

    Epimed International is recalling 500 units of RX-2 COUDE Epidural Needles due to a potential incomplete seal that may impact sterility.

    Product
    RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-0067-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling Cobalt HV with Gentamicin bone cement because the sterile Tyvek packaging may have lost its seal, potentially compromising sterility.

    Product
    Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0089-2018·2017-11-15

    Epimed Recalls TUOHY Epidural Needles Due to Potential Sterility Seal Issues

    Epimed International is recalling 263 units of TUOHY Epidural Needles because a partially incomplete seal could impact the product's sterility.

    Product
    TUOHY Epidural Needle, 20g x 3.5in(8.9cm) TW, 10 units, Calibrated, Plastic Hub, Fixed Wing, Sterile, Rx only
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Food)·F-0152-2018·2017-11-15

    Veronica's Treats Recalls Day of the Dead Truffle Cake Pops for Mold

    Veronica's Treats, Inc. is recalling Day of the Dead Truffle Cake Pops because they may be contaminated with mold. The product was distributed in several states.

    Product
    Day of the Dead Truffle Cake Pops in a 10-oz. box, SKU: 162622
    Category
    Food
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-0084-2018·2017-11-15

    BD Vacutainer Blood Collection Tubes Recalled for Incorrect Labeling

    Becton Dickinson is recalling 90,000 blood collection tubes due to incorrect labeling at the case and shelf pack level.

    Product
    BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg Blood Collection Tubes for Microbiological Studies (8.3 mL * 16x100mm) Catalog No. 364960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0066-2018·2017-11-15

    Encore Medical Recalls Cobalt Bone Cement Due to Packaging Seal Loss

    Encore Medical, Lp is recalling 1,815 units of Cobalt MV with Gentamicin bone cement because the sterile Tyvek packaging seal was lost.

    Product
    Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0064-2018·2017-11-15

    Biomet Cobalt HV Bone Cement Recalled for Packaging Seal Loss

    Encore Medical is recalling Biomet Cobalt HV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0071-2018·2017-11-15

    Aaren Scientific AERO IOL Injection System Recalled for Incorrect Storage Labeling

    Aaren Scientific Inc. is recalling 786 boxes of AERO IOL Injection Systems because the recommended storage temperature on the label is incorrect.

    Product
    AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on the label is Aaren Scientific Inc., Ontario, CA. Used to fold and insert the firm's IOL's.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0082-2018·2017-11-15

    Invivo Recalls Xper Flex Cardio PhysioMonitoring Systems Due to Communication Errors

    Invivo Corporation is recalling 529 Xper Flex Cardio PhysioMonitoring systems because of intermittent communication issues between the host system and the device.

    Product
    Xper Flex Cardio PhysioMonitoring system The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular disease when non-invasive indicators warrant such. Its users, responsible to interpret the data made available, will be…
    Category
    Medical Device
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-0088-2018·2017-11-15

    Epimed COUDE Blunt Nerve Block Needle Recall for Sterility Concerns

    Epimed International is recalling COUDE Blunt Nerve Block Needles due to a potential seal defect that may compromise sterility.

    Product
    COUDE Blunt Nerve Block Needle, 10 units, 0.71mm (22 Ga) x 152mm, Each Unit Contains One Blunt Nerve Block Needle and One Wing, Sterile
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Drugs)·D-0072-2018·2017-11-15

    Doan's Pain Relieving Cream Recalled for Packaging Labeling Mismatch

    Dr. Reddy's is recalling Doan's Pain Relieving Cream because the lot number on the outer packaging does not match the bottle. This is a Class III labeling recall.

    Product
    Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V714000·2017-11-14

    Mercedes-Benz Recalls 2017 Models for Power Steering Overheating Risk

    Mercedes-Benz is recalling 72 vehicles from 2017 models due to a power steering control unit defect that may disable assist, increasing crash risk.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S600, S65 AMG, E300, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V713000·2017-11-14

    Mercedes-Benz Recalls 2016-2017 G-Class Vehicles for ESP Malfunction

    Mercedes-Benz is recalling 2016-2017 G550, G63, and G65 vehicles because an ESP malfunction may prevent the engine from reducing power, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G65, G63, G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18028·2017-11-14

    Go Wheels Hoverboards Recalled Due to Fire and Explosion Hazards

    Four Star Imports is recalling Go Wheels self-balancing scooters sold at Village Mart because the lithium-ion batteries can overheat, posing fire and explosion risks.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V726000·2017-11-14

    Isuzu and Chevrolet Trucks Recall Defective Fire Extinguishers

    Isuzu is recalling certain 2008-2018 Isuzu and Chevrolet trucks because the installed fire extinguishers may clog, require excessive force to activate, or detach, posing injury risks.

    Product
    ISUZU — ISUZU, CHEVROLET NRR, NQR, NPR XD, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide