The Recall Desk

State

Louisiana product recalls

72,984 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,922
Critical
1,094
Severe
1,483
Most recent
2026-09-09

Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.

These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7676–7700 of 79906

  • HighNHTSA·25V164000·2025-03-14

    Ford transmission valve bodies may have been machined incorrectly

    Ford is recalling certain 2024-2025 vehicles because the transmission valve body may have been machined incorrectly, causing reverse gear failure or unexpected forward movement.

    Product
    FORD — FORD, LINCOLN F-150, EXPLORER, RANGER, BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V165000·2025-03-14

    Ford Escape fuel injector repair under earlier recalls was incorrect

    Ford is recalling certain Escape and Bronco Sport vehicles previously repaired incorrectly under recalls 22V-859 or 24V-187, because a fuel injector may crack and leak fuel.

    Product
    FORD — FORD ESCAPE, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V168000·2025-03-14

    Ford Recalls 2022-2023 Transit Vehicles for HVAC Defrost Control Failure

    Ford is recalling 2022-2023 Transit vans previously repaired under recall 22V-791 because the defrost and defog controls may stop working, reducing visibility and increasing crash risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V158000·2025-03-14

    Ford Bronco Sport battery charge detection repair was performed incorrectly

    Ford is recalling certain Bronco Sport and Maverick vehicles previously repaired incorrectly under recall 24V-267, because control modules may not detect a low 12-volt battery charge.

    Product
    FORD — FORD BRONCO SPORT, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V156000·2025-03-13

    GM Recalls BrightDrop Zevo Vehicles for Steering Shaft Defect

    General Motors is recalling 2023-2024 BrightDrop Zevo 600 and 2024 Zevo 400 vehicles because a damaged steering shaft may cause the steering to lock up, increasing crash risk.

    Product
    BRIGHTDROP — BRIGHTDROP ZEVO 400, ZEVO 600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25169·2025-03-13

    Sublue Mix Underwater Scooters Recalled for Lithium-Ion Battery Fire Hazard

    Sublue is recalling about 40,370 Mix underwater scooters and batteries with lithium-ion cells that can overheat and catch fire. Reports include 8 fires, 1 injury, and significant property damage.

    Product
    Sublue Mix underwater scooters and replacement batteries (black batteries only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25182·2025-03-13

    Onasti Toddler Tower Stools Recalled for Fall and Injury Risk

    Onasti Toddler Tower Stools sold on Amazon can collapse or tip over while in use, posing fall and injury risks. Recalls follow four reports of incidents, including injuries.

    Product
    Onasti Toddler Tower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25178·2025-03-13

    Retractable Safety Gates Recalled for Risk of Child Entrapment

    HabiLife Direct retractable safety gates (model SG021) are recalled due to an entrapment hazard where children's torsos can fit through gaps between the gate and floor. About 880 units sold on Amazon from September 2024 through January 2025.

    Product
    Retractable Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25180·2025-03-13

    Chews Life Recalls Silicone Rosary and Decade Teethers for Choking Hazard

    About 5,700 Chews Life Silicone Rosary and Decade teethers are being recalled because the safety snap clasp can detach, posing a choking hazard to infants. No injuries have been reported.

    Product
    Silicone Rosary and Decade teethers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25181·2025-03-13

    Climbing Harness Recalled for Potential Degradation and Fall Risk

    Black Diamond Equipment recalls BD Vision climbing harnesses due to potential degradation that could cause harness failure and falls. No injuries have been reported to date.

    Product
    BD Vision Climbing Harness
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25183·2025-03-13

    Gerolsteiner Sparkling Water Bottles Recalled Due to Laceration Hazard

    Gerolsteiner 750ml sparkling water bottles sold at Trader Joe's locations are being recalled because the glass bottles can crack, creating a laceration hazard. No injuries have been reported.

    Product
    Gerolsteiner 750ml Sparkling Water Bottles
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25E019000·2025-03-13

    Zoox Robotaxi Recall for Unexpected Hard Braking Software Defect

    Zoox is recalling 2023-2024 Robotaxis because a software defect may cause unexpected hard braking in certain driving scenarios, increasing crash risk.

    Product
    ZOOX — ZOOX ZOOX ROBOTAXI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25177·2025-03-13

    BMC recalls Kaius 01 bicycles and framesets for fork separation hazard

    BMC recalled about 1,300 Kaius 01 bicycles because the fork steerer tube can crack and separate during use, posing a fall hazard. No injuries reported; consumers should stop using them and contact dealers for free fork replacement.

    Product
    BMC-branded Kaius 01 bicycles and framesets
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25179·2025-03-13

    Meijer Recalls Konwin Desktop Heaters Due to Fire and Burn Hazards

    Meijer is recalling about 6,050 Konwin desktop heaters because the fan can fail to turn on, causing the unit to overheat and ignite. The company received eight reports of fans burning and melting, but no injuries have been reported.

    Product
    Konwin Desktop Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1257-2025·2025-03-12

    Insulin pump recall: Medtronic Paradigm models malfunction during airplane flight

    Medtronic MiniMed's Paradigm insulin pumps can malfunction during airplane flight due to air pressure changes, potentially causing dangerously high or low blood sugar levels that could be fatal.

    Product
    Paradigm insulin pump, REF: MMT-754
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0588-2025·2025-03-12

    Watermelon and Cucumber Products Recalled for Potential Salmonella Contamination

    JFE Franchising is recalling watermelon and cucumber products with Tajin seasoning due to potential Salmonella contamination. Affected packages were distributed in TX, LA, WY, and AZ with sell-by dates from October 12 through December 5, 2024.

    Product
    Mixed Melon, Cucumber & Tajin 18 oz Watermelon & Cucumber w/ Tajin 18 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-1244-2025·2025-03-12

    Rotarex Atherectomy Catheter Recalled for Helix Fracture Risk

    Bard is recalling Rotarex Atherectomy System catheters due to potential helix fracture or breakage that could cause vessel injury and severe bleeding. Updated instructions are being distributed to clarify procedural steps to reduce this risk.

    Product
    Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1205-2025·2025-03-12

    FDA Recalls VARIPULSE Bi-Directional Ablation Catheter Due to Neurovascular Events

    Biosense Webster is recalling VARIPULSE Bi-Directional Ablation Catheters (REF D141201) due to an observed trend of neurovascular events. The FDA issued a Class I recall affecting approximately 497 units distributed worldwide.

    Product
    VARIPULSE Bi-Directional Ablation Catheter REF D141201. The Field Catheter is indicated for use in catheter based cardiac electrophysiological mapping (stimulating and recording) and, when used for TRUPULSE Generator, for the treatment of drug refractory recurrent symptomat
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·F-0585-2025·2025-03-12

    Garden Salad Products Recalled for Potential Salmonella Contamination

    JFE Franchising is recalling garden salad products due to potential Salmonella contamination. Products were distributed in Texas, Louisiana, Wyoming, and Arizona.

    Product
    Garden Salad 12 oz Family Garden Salad 24 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0589-2025·2025-03-12

    Cobb Salad Products Recalled for Potential Salmonella Contamination

    JFE FRANCHISING INC is recalling Cobb Salad products (22 oz and 11 oz packages) due to potential Salmonella contamination. Products were distributed in Texas, Louisiana, Wyoming, and Arizona.

    Product
    Family Cobb Salad 22 oz Cobb Salad 11 oz packed in clamshells
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0606-2025·2025-03-12

    Amazon Fresh Jumbo Sugar Cookies recalled for undeclared egg allergen

    Amazon Retail LLC is recalling Amazon Fresh Jumbo Sugar Cookies nationwide due to undeclared egg, a major allergen. Consumers with egg allergies should not consume the affected cookies.

    Product
    ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12 count), product is baked and packaged in flexible plastic bag. 4-day shelf life. UPC 465712007998. ASIN B084PX9V31, Amazon Fresh Jumbo Sugar Cookie, 2.3 oz (1 count), product is baked and sold from open pastry tray in s
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1246-2025·2025-03-12

    Medtronic Pipeline Vantage device recall: deformation may cause blood clots

    The Pipeline Vantage Embolization Device may malfunction, with the braid deforming or not positioning correctly, potentially causing blood clots. Approximately 7,820 units are affected worldwide.

    Product
    Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20, PED3-021-250-20, PED3-021-300-16, PED3-021-300-20, PED3-021-275-12, PED3-021-275-16, PED3-021-325-12, PED3-021-325-14, PED3-021-325-16, PED3-021-325-20,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1263-2025·2025-03-12

    Insulin Pump Recalled for Abnormal Delivery During Flight Pressure Changes

    Medtronic MiniMed 720G insulin pumps may malfunction during airplane travel due to air pressure changes, causing abnormal insulin doses that can lead to severe low or high blood sugar emergencies.

    Product
    MiniMed insulin pump, REF: 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
    Category
    Medical Device
    Distribution
    Distributed nationwide