The Recall Desk

State

Louisiana product recalls

73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,967
Critical
1,107
Severe
1,740
Most recent
2026-11-14

Of the 6,967 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 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52176–52200 of 80800

  • ModerateFDA (Devices)·Z-2338-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 60 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2334-2016·2016-08-10

    Zimmer Air Dermatome II Handpieces Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 630 Air Dermatome II handpieces because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Handpiece, item number 00-8851-001-00. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2317-2016·2016-08-10

    Medtronic Navigation Recalls Fusion ENT Software Application

    Medtronic Navigation is voluntarily recalling 27 units of the Fusion ENT software application due to a field action involving Neurologica scanners.

    Product
    Fusion ENT Application. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2302-2016·2016-08-10

    Ortho-Clinical Diagnostics Recalls VITROS Total T4 Reagent Packs

    Ortho-Clinical Diagnostics is recalling VITROS Total T4 Reagent Packs because test results may show a negative bias before the 8-week storage limit.

    Product
    VITROS Immunodiagnostic Products Total T4 Reagent Pack, REF/Product Code 874 4468, Unique Identifier No. 10758750005147, IVD --- Ortho-Clinical Diagnostics, For in vitro diagnostic use only. For the quantitative measurement of total thyroxine (T4) in human serum and plasma…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2320-2016·2016-08-10

    Implant Direct Recalls RePlant Angled Abutments Due to Design Defect

    Implant Direct Sybron Manufacturing is recalling 205 RePlant Angled Abutments because they are oversized due to a design specification issue.

    Product
    RePlant¿ Angled Abutment Part Number 6050-52-60
    Category
    Medical Device
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-2318-2016·2016-08-10

    Medtronic Navigation Recalls StealthStation Software Applications

    Medtronic Navigation is voluntarily recalling StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

    Product
    MACH Cranial Treon. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2340-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 110 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 4 inch. Part #00-8851-204-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2314-2016·2016-08-10

    Medtronic Navigation Recalls StealthStation Software Applications

    Medtronic Navigation is conducting a voluntary field action for StealthStation software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

    Product
    FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2315-2016·2016-08-10

    Medtronic Navigation Recalls S7 MACH FrameLink Software Applications

    Medtronic Navigation is conducting a voluntary field action for S7 MACH FrameLink software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

    Product
    S7 MACH FrameLink. The software application is sent in CD format with an IFU, wrapped in plastic with a label for shipping purposes. Product Usage: The StealthStation System is intended as an aid for precisely locating anatomical structures in either open or percutaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2309-2016·2016-08-10

    Beckman Coulter AU680 Chemistry Analyzers Recalled for Leaking C Cups

    Beckman Coulter is recalling AU680 Chemistry Analyzers because leaking and cracked C cups can cause coolant to leak onto circuit boards, resulting in short-circuits and instrument stop mode.

    Product
    AU680 Chemistry Analyzers, Reference No. B04779 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1453-2016·2016-08-10

    Teva Recalls Children's Qnasl Nasal Aerosol for Content Uniformity Failure

    Teva North America is recalling Children's Qnasl nasal aerosol canisters due to failed spray content uniformity tests. The FDA classified this as a Class III recall.

    Product
    Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal Aerosol, 40 mcg per spray, 60 Metered Sprays per canister, 4.9g Net Contents, Rx only; Professional Sample; Manufactured for Teva Respiratory, LLC, Horsham, PA 19044; By: 3M Drug Delivery Systems, Northridge, CA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2333-2016·2016-08-10

    C.R. Bard Recalls SureStep Urine Collection System for Labeling Issues

    C.R. Bard is recalling 530 SureStep urine collection systems due to a labeling problem. The recall is voluntary and nationwide.

    Product
    SureStep Tray, with Add-a-Foley, COMPLETE CARE, Drainage Bag, and STATLOCK Stabilization The product is a urine collection system that includes a STATLOCK Foley Stabilization Device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2311-2016·2016-08-10

    Branan Medical Recalls AmediCheck Instant Test Cups Due to Packaging Error

    Branan Medical is recalling AmediCheck Instant Test Cups because they may erroneously contain 12-panel cups due to a packaging error.

    Product
    AmediCheck Instant Test Cup, Part No. C-C0501A-3A Product Usage: The AmediCheck Instant Test Cup is an in vitro diagnostic test for the rapid detection of the following drugs in human urine. Drug Analyte Cut off Device Code Marijuana THC 50 ng/mL THC Cocaine Benzoylecgonine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16239·2016-08-09

    Kohler Recalls Portable Generators Due to Electrical Shock Hazard

    Kohler Power Systems is recalling specific portable generator models due to a wiring error that creates an electrical shock risk. Consumers should stop using these units and contact Kohler for a free repair.

    Product
    Kohler portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16240·2016-08-09

    Brown Jordan Recalls Swivel Patio Chairs Due to Fall Hazard

    Brown Jordan Services is recalling Hampton Bay swivel patio chairs because the base can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.

    Product
    Swivel Dining and Lounge Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V586000·2016-08-08

    KME Predator Fire Apparatus Recalled for Touchscreen Malfunctions

    KME is recalling specific Predator fire apparatus vehicles because touchscreen malfunctions may cause accessories to turn on or off unexpectedly, increasing crash risk.

    Product
    KME — KME PREDATOR TRACTOR AERIAL, 7600 TANKER, PREDATOR PANTHER RESCUE, PREDATOR PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V584000·2016-08-05

    Eldorado E-Z Rider II Transit Bus Recall for Tire Clearance Issue

    Eldorado is recalling 2016 E-Z Rider II transit buses because front steel rims may allow tires to contact tie-rods, risking sudden air loss and crashes.

    Product
    ELDORADO — ELDORADO E-Z RIDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E068000·2016-08-05

    WSB Recalls WSB777 Half Helmets for Insufficient Crash Protection

    WSB Inc is recalling WSB777 half helmets manufactured in May 2015 because they may lack required labeling and fail to provide adequate head protection in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V585000·2016-08-05

    Pierce Fire Trucks Recalled for Transmission Shift Unit Defect

    Pierce Manufacturing is recalling 2015-2016 fire trucks because a damaged transmission component may prevent operators from switching power output to the water pump.

    Product
    PIERCE — PIERCE SABER, VELOCITY, DASH CF, ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16766·2016-08-04

    Cinmar Recalls Magnetic Travel Maps Due to Magnet Ingestion Risk

    Cinmar is recalling World Magnetic Travel Maps sold at Frontgate because the included magnets pose a serious ingestion hazard to children.

    Product
    Magnetic travel maps with magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V583000·2016-08-04

    Smeal Fire Trucks Recalled for Transmission Shift Unit Defect

    Smeal is recalling 88 model year 2015-2016 Aerial and Pumper fire trucks because a damaged transmission component may prevent operators from switching power output, potentially hindering fire suppression.

    Product
    SMEAL — SMEAL AERIAL FIRE APPARATUS, AERIAL, PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V581000·2016-08-04

    Ferrara Fire Trucks Recalled for Transmission Shift Unit Defect

    Ferrara is recalling 2015-2016 fire trucks because a damaged transmission component may prevent operators from switching power output, potentially disabling water pumps.

    Product
    FERRARA — FERRARA IGNITER, CINDER, INTRUDER, INFERNO
    Category
    Vehicle
    Distribution
    Distributed nationwide