The Recall Desk

State

Louisiana product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41376–41400 of 80772

  • ModerateFDA (Devices)·Z-2430-2018·2018-07-25

    Valeris Medical Recalls Apollo XT Suture Anchors Due to Material Mislabeling

    Valeris Medical is recalling 113 Apollo XT Suture Anchors because the labels incorrectly identified the material as titanium instead of PEEK.

    Product
    Apollo XT Suture Anchor, 5.5 x 15 Product Usage: Apollo XT Suture Anchors are intended for: Shoulder - Rotator Cuff Repair - Bankart Repair - SLAP Lesion Repair - Biceps Tenodesis - Acromio-Clavicular Separation Repair - Deltoid Repair - Capisular Shift or Capsulolabral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2468-2018·2018-07-25

    Fx Solutions Proton Beam Therapy Heads Recalled for Blister Breach

    Fx Solutions is recalling specific proton beam therapy heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS CENTERED HEAD CoCr 50x19, REF 106-5019 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2483-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Leaking Gatorade Pouches

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, No Spiro Diabetes. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2469-2018·2018-07-25

    Fx Solutions Offset Heads Recalled for Blister Breach

    Fx Solutions is recalling specific lots of Humelock Offset Heads due to a breach in the external blister packaging.

    Product
    Fx SOLUTIONS OFFSET HEAD CoCr 50x20, REF 106-5000 Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2442-2018·2018-07-25

    Health Harmony Mobile App Recalled for Data Synchronization Delays

    Intel-GE Care Innovations LLC is recalling the Health Harmony Mobile application because patient data sometimes failed to sync with the backend database in a timely manner.

    Product
    Health Harmony Mobile application software Product Usage: Care Innovations Health Harmony Mobile is intended as a communication tool to display medical device data from third party devices for patients to view, and to collect assessment (question & answers) from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2438-2018·2018-07-25

    Siemens Dimension Vista MULTI 2 SDIL Diluent Recall for Defective Septum

    Siemens is recalling 1,195 units of Dimension Vista MULTI 2 SDIL diluent because a defective septum may cause erroneously elevated test results.

    Product
    Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
    Category
    Medical Device
    Distribution
    53 states
  • ModerateFDA (Devices)·Z-2481-2018·2018-07-25

    Cardinal Health Recalls Presource PBDS Kits Due to Gatorade Pouch Seal Defect

    Cardinal Health is recalling 8,928 Presource PBDS kits because a defect in the Gatorade pouch seal caused the pouch to leak within the kit.

    Product
    Presource PBDS, Kit, Common. Kit includes a exerciser volumetric 5000 ML device, two items of cloth, skin prep 2% CHG, a packet of 4 chlorhexidine gluconate antiseptic cloths, and Gatorade pouches. Product Usage: The kit is provided to a patient pre-surgery, as part of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E060000·2018-07-24

    SynTec Recalls School Bus Seats Due to Mounting Foot Defect

    SynTec is recalling S3B 45-inch Restraint School Bus Seats because the mounting foot may pull through the bolted joint at the bus floor, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18192·2018-07-24

    JCPenney Recalls Okie Dokie Shorts Due to Choking Hazard

    JCPenney is recalling Okie Dokie Denim Patches Shortie shorts because the patches can detach, posing a choking hazard to young children.

    Product
    Okie Dokie Denim Patches Shortie shorts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18190·2018-07-24

    Ross Stores Recalls Bistro Chairs Due to Frame Breakage and Fall Hazard

    Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V488000·2018-07-23

    Karma Revero Recalled for Non-Compliant Driver Side Rearview Mirror Glass

    Karma Automotive is recalling 2018 Revero vehicles because the driver's side exterior rearview mirror may use convex glass instead of flat glass, failing federal safety standards.

    Product
    KARMA — KARMA REVERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E058000·2018-07-20

    Meritor Recalls Wheel Studs Due to Potential Heat Treatment Defect

    Meritor is recalling specific wheel studs installed in steer axle hubs because improper heat treatment may cause them to fail, potentially leading to wheel detachment.

    Product
    WHEELS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E059000·2018-07-20

    Jost Recalls Fifth Wheel Assemblies Due to Narrow Bracket Risk

    Jost International is recalling certain Outboard Sliders because a narrow bracket may allow the trailer to separate from the tractor, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V489000·2018-07-20

    BraunAbility Recalls Wheelchair Vans Due to Brake Line Connection Defect

    Braun Corporation is recalling 2012-2018 BraunAbility Dodge and Chrysler wheelchair vans because brake lines may be disconnected, reducing electronic stability control performance.

    Product
    BRAUNABILITY — BRAUNABILITY DODGE WHEELCHAIR VAN, CHRYSLER WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V487000·2018-07-20

    Freightliner Recalls M2 Trucks for Steering Shaft Installation Defect

    Daimler Trucks is recalling 2018-2019 Freightliner Business Class M2 trucks because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V472000·2018-07-20

    Van-Con Recalls School Buses Due to Seat Foam Crash Protection Defect

    Van-Con is recalling 2011-2018 33803 Dual Rear Wheel school buses because seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    VAN-CON — VAN-CON 33803 DUAL REAR-WHEEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-07202018-1·2018-07-20

    FSIS Public Health Alert for Hungry Man Dinners with Recalled Whey Powder

    The USDA FSIS issued a public health alert for Hungry Man frozen dinners containing whey powder recalled due to possible Salmonella contamination. No adverse reactions have been reported.

    Product
    FSIS Issues Public Health Alert For Products Containing FDA-Regulated Whey Powder That Has Been Recalled Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V480000·2018-07-19

    Ducati Recalls 2018 Motorcycles Due to Rear Brake Pad Defect

    Ducati is recalling 2018 Panigale and Hypermotard motorcycles because rear brake pad friction material may detach, increasing stopping distance and crash risk.

    Product
    DUCATI — DUCATI PANIGALE V4, HYPERMOTARD, PANIGALE 959, PANIGALE 1299 FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V482000·2018-07-19

    Thor Outlaw Motorhomes Recalled for Missing Rear Reflectors

    Thor Motor Coach is recalling 2018-2019 Outlaw motorhomes because they lack required rear reflex reflectors, which reduces visibility to other drivers.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1009-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Red Kapuas Hulu , 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1013-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling Gaia Kratom powder due to FDA-confirmed Salmonella contamination. Consumers should stop using the product.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White MD, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide