The Recall Desk

State

Louisiana product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5576–5600 of 79862

  • SevereCPSC·25455·2025-09-04

    Cordless grease guns recalled after hose failures caused five laceration injuries

    About 62,927 Makita professional cordless grease guns and grease gun hoses are recalled because the flexible hose can develop a hole and eject grease. Five hose failures with laceration injuries were reported.

    Product
    Makita Professional Cordless Grease Guns and Makita Grease Gun Hoses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V575000·2025-09-04

    2025 Jeep Wagoneer S Recalled for Incorrect Cross Beam

    Chrysler is recalling certain 2025 Jeep Wagoneer S vehicles with an incorrect cross car beam in the instrument panel. The defect may not adequately protect occupants in a crash.

    Product
    JEEP — JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V574000·2025-09-04

    2025 Jeep Wagoneer S Incorrectly Installed Spring Disables Park Function

    Chrysler recalls 2024-2025 Jeep Wagoneer S and Dodge Charger electric vehicles due to an incorrectly installed spring that may disable the park function, potentially causing vehicle rollaway.

    Product
    DODGE — DODGE, JEEP CHARGER EV, WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V578000·2025-09-04

    Jayco Recalls 2026 Seismic Fifth Wheels for Incorrect Weight Labels

    Jayco is recalling 2026 Seismic fifth wheel travel trailers because the certification label lists an incorrect Gross Axle Weight Rating (GAWR).

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL SEISMIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V580000·2025-09-04

    IC Bus School Buses Recalled for Structural Reinforcement Defect

    International Motors is recalling certain 2016-2026 IC Bus CESB and 2016-2021 RESB school buses due to missing or incomplete underfloor reinforcement that may compromise crash safety. Owners should contact a dealer for free inspection and installation.

    Product
    IC BUS — IC BUS CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V573000·2025-09-04

    2025 Chrysler Pacifica side curtain air bags recalled for inadequate pressure retention

    Chrysler is recalling certain 2025 Pacifica and Voyager vehicles due to defective side curtain air bags. The air bags may have insufficient pressure retention from improperly sealed seams, increasing the risk of ejection during a crash.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V577000·2025-09-04

    2023–2025 Toyota BZ4X, Lexus RZ, and Subaru Solterra HVAC Defroster System Recall

    Toyota is recalling certain 2023–2025 BZ4X, Lexus RZ, and Subaru Solterra vehicles because the defroster and defogger system may become inoperative due to electrical compressor failure, decreasing driver visibility and increasing crash risk.

    Product
    LEXUS — LEXUS, TOYOTA, SUBARU RZ, BZ4X, SOLTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25458·2025-09-04

    Firearm chamber locks recalled because they can be forcibly removed

    About 300 AR-15 Chamber Lock Pro firearm locks shipped between June 2 and July 15, 2025 are recalled because a manufacturing defect allows them to be forcibly removed, permitting access to the firearm.

    Product
    AR-15 Chamber Lock Pro Firearm Locks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2343-2025·2025-09-03

    Insulin pumps recalled over malfunction that stops insulin delivery and alerts

    Tandem t:slim X2 insulin pumps built with Revision A and B speakers may hit Malfunction 16, losing audible alerts and stopping insulin delivery. The FDA classified the action as Class I. 171,750 units are affected.

    Product
    Battery Operated infusion pumps. t:slim X2 G5, Replacement, Refurbished, REF: 1000911; t:slim X2 GS Classic, Replacement, Refurbished, REF: 1003808; t: slim X2, Basal-IQ, mg/dl, REF: 1004219; Pump, t:slim X2, Clinical Use Only, REF: 1004484; Pump, t:slim X2, Control-IQ, REF:
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2460-2025·2025-09-03

    Reprocessed electrophysiology catheters recalled over small residual particulates in specific lots

    Medline ReNewal reprocessed St. Jude Medical diagnostic electrophysiology catheters are recalled because specific lots may contain small residual particulates. The FDA classified the action as Class I.

    Product
    Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic Electrophysiology Catheter Models 401150RH, 401206RH, 401207RH, 401210RH, 401211RH, 401212RH, 401222RH, 401223RH, 401226RH, 401227RH, 401228RH, 401260RH, 401261RH, 401271RH, 401305RH, 401306RH, 401309RH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2462-2025·2025-09-03

    Foley catheters recalled because obstructed lumen may prevent bladder drainage

    Bardex Lubri-Sil I.C. Foley catheters and related tray systems are recalled because the catheter may have an obstructed lumen, which may prevent the bladder from draining. 175,158 units are affected.

    Product
    Bardex Lubri-Sil I.C. 400-series Temperature Sensing Silver/Hydrogel Coated All-Silicone Foley Catheter 5cc Balloon, REF: 119314; SureStep Foley Tray System Lubri-Sil I.C. Complete Care, REF: A319514A; Bard Silver Lubri-Sil Foley Tray Temperature Sensing with Bard Hydrogel and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2471-2025·2025-09-03

    Hysterectomy procedure packs recalled over unconfirmed sterilization assurance requirements

    American Contract Systems robotic and vaginal hysterectomy packs are recalled because the firm cannot confirm that product sterilization assurance requirements were met. 50 units are affected.

    Product
    AMERICAN CONTRACT SYSTEMS, Medical Procedure kits and trays labeled as: 1) ROBOT HYST PACK, MODEL/ITEM NUMBER GRRB10E; 2) VAG HYST PACK, MODEL/ITEM NUMBER SPVH62P.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2342-2025·2025-09-03

    C-arm imaging systems recalled over missing lead tape in collimator covers

    GE HealthCare OEC 9800 and OEC 9900 Elite C-arm systems are recalled because impacted units are missing the full layer of lead tape in the collimator covers, slightly increasing radiation exposure.

    Product
    GE HealthCare OEC 9900 Elite C-arm Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2443-2025·2025-09-03

    Phantom Essential loupe kits recalled because nickel nose pads may cause allergy

    Orascoptic Phantom Essential Kits are recalled because loupe nose pads containing nickel may cause an allergic reaction, following complaints. 74 kits are affected.

    Product
    Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0599-2025·2025-09-03

    Lisdexamfetamine 40 mg bottles recalled after being filled with 30 mg capsules

    Lisdexamfetamine Dimesylate Capsules 40 mg, lot 25280726A, distributed by Lannett, are recalled because a bottle labeled 40 mg contained 30 mg capsules. 8,544 bottles are affected.

    Product
    LISDEXAMFETAMINE DIMESYLATE — LISDEXAMFETAMINE DIMESYLATE (LISDEXAMFETAMINE DIMESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0534-2025·2025-09-03

    Everything bagel mix recalled because label omits sesame and other ingredients

    Baker's Authority Everything Bagel Mix in 1 lb and 5 lb bags is recalled because the label does not list its ingredients, including the major food allergen sesame. 197 units are affected.

    Product
    Baker's Authority Everything Bagel Mix; 5lb bag and 1lb bag; stored dry at room temperature; packaged in silver bag
    Category
    Food
    Distribution
    17 states
  • HighFDA (Food)·H-0577-2025·2025-09-03

    Hostess Ding Dongs recalled over mold traced to malfunctioning cooler

    Hostess Ding Dongs in twin packs and 10- and 16-count cartons are recalled for mold, which the firm traced to a malfunctioning cooler after customer complaints rose. 60,630 cases are affected.

    Product
    Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7 oz) UPC 8 88109 11061 1; 16-1.28 oz carton (20.31 oz) Individual selling unit - UPC 8 88109 01182 6 16-count selling unit - UPC 8 88109 11092 5
    Category
    Food
    Distribution
    42 states
  • HighFDA (Drugs)·D-0603-2025·2025-09-03

    H-E-B alcohol pads recalled for isopropyl alcohol below labeled concentration

    H-E-B inControl Sterile Alcohol Pads, 100 per container, are recalled nationwide because isopropyl alcohol levels fall below the labeled concentration. The recall covers 300,000 pads.

    Product
    INCONTROL ALCOHOL — INCONTROL ALCOHOL (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0598-2025·2025-09-03

    Sucralfate tablets recalled after bankruptcy left quality program unmonitored

    Sucralfate Tablets USP 1 gram from American Health Packaging are recalled because the firm's Chapter 11 filing left it unable to monitor its quality program. 26,992 blister packs are affected.

    Product
    Sucralfate Tablets, USP 1 gram, 100 Tablets, (10x10), Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 NDC 60687-695-01 - Carton NDC [60687-695-11- Unit Dose]
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0533-2025·2025-09-03

    Three seed baking mix recalled because label omits sesame and other ingredients

    Baker's Authority Three Seed Mix in 5 lb bags is recalled because the label does not list ingredients, including the major food allergen sesame. Millet and flax are also undeclared. 78 units are affected.

    Product
    Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bag
    Category
    Food
    Distribution
    17 states