The Recall Desk

State

Louisiana product recalls

73,486 recalls have nationwide distribution and so reach Louisiana. 6,959 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,959
Critical
1,109
Severe
1,737
Most recent
2026-10-14

Of the 6,959 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,737 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,959 recalls whose distribution notice names Louisiana specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22826–22850 of 80445

  • ModerateFDA (Devices)·Z-0954-2022·2022-04-27

    Medical Device Reference Standard Recalled for Inadequate Quality Control Process

    Microbiologics Inc recalls an inactivated Mycoplasma genitalium reference standard (Lot HE0069-02-1) because its quality control process did not meet specification requirements. This reference material is used in diagnostic and laboratory testing.

    Product
    Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0971-2022·2022-04-27

    X-Ray Imaging System Cooling Circuit Failure Recall

    Siemens is recalling Artis zee floor MN X-ray systems due to a potential cooling circuit malfunction. If coolant drops below adequate levels, the X-ray tube may not cool properly and the system will automatically shut down.

    Product
    Artis zee floor MN, Model Number 10094142
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0955-2022·2022-04-27

    Inactivated Mycoplasma genitalium reference material recalled due to inadequate QC

    Microbiologics Inc is recalling an inactivated Mycoplasma genitalium reference material (Catalog # HE0070N, Lot HE0070-01-1) because the quality control process did not meet specification requirements.

    Product
    Inactivated macrolide-resistant Mycoplasma genitalium
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0784-2022·2022-04-27

    Hand Sanitizer Recalled Over Manufacturing Quality Deviations

    VIRGIN SCENT INC has recalled 46,368 bottles of artnaturals Hand Sanitizer nationwide due to manufacturing process deviations. The affected lots were produced using common ingredients from a contaminated batch.

    Product
    artnaturals Hand Sanitizer
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0956-2022·2022-04-27

    Abbott TactiCath Ablation Catheter Disabled by Preprogrammed First-Use Date

    Abbott is recalling 2,134 TactiCath ablation catheters manufactured with a preprogrammed 'First Use Date' that disables the device. Affected devices with 37 specific lot numbers were distributed in the U.S. and 21 other countries.

    Product
    Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve D-F, Model A-TCSE-DF, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0948-2022·2022-04-27

    Baxter Syringe Tip Caps Recalled Due to Incorrect Labeling

    Baxter is recalling DISCPAC syringe tip caps that are mislabeled as self-righting when they do not possess this capability, risking improper use in medical procedures.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0949-2022·2022-04-27

    Terumo Cardiovascular Procedure Kit Recall for Shipping Damage

    Terumo Cardiovascular Systems Corp is recalling two lots of cardiovascular procedure kits due to packaging damage that occurred during shipping. The recall affects 64 units distributed in California and Indiana.

    Product
    Cardiovascular Procedure Kit catalog # 76645 & 73806
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0773-2022·2022-04-27

    Diclofenac Sodium Topical Solution Recalled Due to Manufacturing Quality Deviations

    Preferred Pharmaceuticals, Inc. is recalling Diclofenac Sodium Topical Solution because the manufacturing firm discontinued its stability study program, a CGMP violation. All products within their expiration dates are affected.

    Product
    Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0968-2022·2022-04-27

    X-ray Imaging System Cooling Failure May Cause Tube Overheating

    Siemens Artis zee ceiling X-ray systems may fail to cool the X-ray tube if the coolant level drops. The system will automatically block X-ray emissions and display warning messages to prevent equipment damage.

    Product
    Artis zee ceiling, Model Number 10094137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0984-2022·2022-04-27

    Beckman Coulter IRISpec CA Control glucose measurement failures recalled

    Beckman Coulter is recalling IRISpec CA/CB/CC control kits due to failures in glucose measurement for the CA Control component. The recall affects laboratory quality control products distributed worldwide.

    Product
    Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles each of CA Control, CB Control, and CC Control.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0783-2022·2022-04-27

    FDA Recalls artnaturals Scent-Free Hand Sanitizer for Manufacturing Deviations

    artnaturals Scent-Free Hand Sanitizer is recalled due to manufacturing process deviations. Approximately 570,268 bottles distributed nationwide are affected.

    Product
    artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0981-2022·2022-04-27

    Oral DNA Collection Device Recalled for Evaporating Stabilizing Liquid

    DNA Genotek Inc. is recalling ORAcollect Dx oral DNA collection devices because the stabilizing liquid can evaporate, reducing shelf life and potentially affecting sample preservation.

    Product
    ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012, OCD-100.014+ACP078, OCD-100.014+ACP078, OCD-100.032 and OCD-100A, OCD-100A.022, OCD-100A.023, OCD-100A.024, OCD-100A.025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0980-2022·2022-04-27

    Artis Q.zen Biplane X-ray Systems Coolant Level Failure Recall

    Siemens is recalling 69 Artis Q.zen biplane systems where coolant levels may drop sufficiently to prevent adequate X-ray tube cooling, triggering automatic shutdown safeguards.

    Product
    Artis Q.zen biplane, Model Number 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2022·2022-04-27

    Oral RNA Collection Kit Recalled Due to Stabilizer Evaporation

    DNA Genotek Inc. is recalling ORAcollect RNA: ORE-100 kits due to evaporation of the stabilizing liquid, which reduces shelf life. Approximately 17,080 units are affected, including lot YJ530.

    Product
    ORAcollect RNA: ORE-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V278000·2022-04-26

    Porsche Taycan seat wire harness defect may deactivate airbags

    Porsche is recalling certain 2020-2021 Taycan vehicles because the driver and passenger seat wire harness could become damaged during horizontal seat adjustment. A damaged harness may deactivate airbags, increasing crash injury risk.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·011-2022·2022-04-25

    Lakeside Refrigerated Services Recalls Ground Beef Due to E. coli O103 Risk

    Lakeside Refrigerated Services is recalling approximately 120,872 pounds of ground beef products due to possible E. coli O103 contamination. The products were shipped to retail locations nationwide.

    Product
    Lakeside Refrigerated Services Recalls Ground Beef Products Due to Possible E. coli O103 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V277000·2022-04-25

    PACCAR Recalls Kenworth and Peterbilt Trucks for Steering Fastener Defect

    PACCAR is recalling 2018-2020 Kenworth and Peterbilt trucks because steering arm fasteners may fail, potentially causing loss of steering control.

    Product
    KENWORTH — KENWORTH, PETERBILT T270, 579, T440, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V276000·2022-04-25

    Gillig Recalls 2014-2021 Low Floor Buses Due to Engine Start Risk

    Gillig is recalling 2014-2021 Low Floor transit buses because rear-mounted ultracapacitors may allow the engine to start unexpectedly while the master battery disconnect switch is off.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V272000·2022-04-22

    Thomas Built Buses Recalling HDX Models for Battery Cable Fire Risk

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Bus HDX commercial buses because an improperly routed battery cable may chafe and cause an electrical short circuit, increasing the risk of a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V270000·2022-04-22

    2022 Alliance RV Paradigm Recreational Trailers Recalled for LP Gas Leak

    Alliance RV is recalling certain 2022 Paradigm, Avenue, and Valor recreational trailers due to cracked quick disconnect fittings in the LP gas system that can cause gas leaks, creating a fire hazard.

    Product
    ALLIANCE RV — ALLIANCE RV AVENUE, PARADIGM, VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V271000·2022-04-22

    Thomas Built Buses Recalls HDX School Buses for Fire Risk

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses HDX school buses because a battery cable may chafe and cause a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V273000·2022-04-22

    Tiffin Allegro motorhomes recalled for faulty hydraulic slide cylinders

    Tiffin is recalling certain 2021 and 2022 Allegro and Allegro Bay motorhomes due to defective hydraulic cylinder seals. The slide-room may extend unintentionally, increasing crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO BAY, ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide