The Recall Desk

State

Louisiana product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1401–1425 of 79829

  • HighFDA (Devices)·Z-2313-2026·2026-06-17

    Plum Duo Precision IV pumps may not display soft limit alerts

    Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Duo Precision IV Pump, 40002-0403
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-1109-2026·2026-06-17

    Neuro Nourish dietary supplement recalled over premature lipid oxidation

    Neuro Nourish, a 6-in-1 nutritional supplement, is being recalled because premature lipid oxidation may give the product an off odor and bitter taste. 512 units affected.

    Product
    NEURO NOURISH dietary supplement; 6-IN-1 PREBIOTIC, PROBIOTIC, VITAMIN, MINERAL, FATTY ACID, AND ANTIOXIDANT NUTRITIONAL SUPPLEMENT TO SUPPORT DRAIN AND GUT HEALTH NET WT. 5.9 OZ; UPC: 310M5951601
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0597-2026·2026-06-17

    Minocycline extended-release tablets failed dissolution testing during stability analysis

    Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, are being recalled after an out-of-specification dissolution result at the ninth month of testing. 360 bottles affected.

    Product
    MINOCYCLINE HYDROCHLORIDE — MINOCYCLINE HYDROCHLORIDE (MINOCYCLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2320-2026·2026-06-17

    EXCOR pediatric blood pump valves carry mismatched inner package expiration dates

    EXCOR Pediatric VAD System blood pump PU valves are being recalled because the inner package expiration date does not match the correct outer package date.

    Product
    EXCOR Pediatric Ventricular Assist Device (VAD) System Blood Pump PU Valves: 10 ml, REF: P10P-001; 30 ml, REF: P30P-001x01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2403-2026·2026-06-17

    Boston Scientific reusable TCN nitinol electrodes may underperform expected levels

    Boston Scientific TCN nitinol electrodes across four lengths are being recalled because the reusable electrodes may not meet expected performance levels. 49,251 units affected.

    Product
    Boston Scientific TCN Electrodes: REF: TCN-5, TCN Electrode, NITINOL, 5 cm x 0.45 mm (0.0175 in); REF:TCN-10, TCN Electrode, NITINOL, 10 cm x 0.45 mm (0.0175 in) REF:TCN-15, TCN Electrode, NITINOL, 15 cm x 0.45 mm (0.0175 in); REF:TCN-20, TCN Electrode, NITINOL, 20 cm x 0.45
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2319-2026·2026-06-17

    Mahurkar Elite PASS trays shipped without the labeled Tegaderm CHG dressing

    Mahurkar Elite PASS Trays are being recalled because the Tegaderm CHG dressing specified in the product labeling was missing from certain lots. 25,627 units are affected.

    Product
    Mahurkar Elite PASS Trays; Description (Product Number/CFN): 12 FR x 13cm Acute Dual Lumen Catheter with Straight Extensions, PASS Tray (8888221413), 12 FR x 16cm Acute Dual Lumen Catheter with Curved Extensions, PASS Tray (8888222416), 12 FR x 16cm Acute Dual Lumen Catheter wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0938-2026·2026-06-17

    Pasteurized donor human milk bottles show dark spot contamination

    MMB of Louisiana Pasteurized Donor Human Milk, 3 oz, is being recalled over potential physical contamination after a dark spot was noticed on the bottom of a container. 32 bottles affected.

    Product
    MMB of Louisiana Pasteurized Donor Human Milk, Volume: 3 oz, Cal/Oz: 19, 0.9 g/dL Protein, packaged in a clear plastic bottle with white plastic cap
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-2355-2026·2026-06-17

    NeoSpan compression staple kits missing Magnetic Resonance Conditional labeling symbol

    NeoSpan SuperElastic Compression Staple kits are being recalled because the Magnetic Resonance Conditional symbol is missing from the carton, inner tray and patient label. 306 kits affected.

    Product
    NeoSpan¿ SuperElastic Compression Staple w/Instruments Catalog Number and Product Name T50 SN010 NeoSpan¿ SuperElastic Compression Staple w/Instruments, Size 10x10x10 UDI-DI Code: 00817906020083 T50 SN012 NeoSpan¿ SuperElastic Compression Staple w/Instruments, Size 12x12x1
    Category
    Medical Device
    Distribution
    25 states
  • ModerateFDA (Devices)·Z-2402-2026·2026-06-17

    Boston Scientific reusable CSK stainless steel electrodes may underperform expected levels

    Boston Scientific CSK stainless steel electrodes across several lengths are being recalled because the reusable electrodes may not meet expected performance levels. 31,923 units affected.

    Product
    Boston Scientific CSK Electrodes: REF: CSK-TC10, CSK Electrode, STAINLESS STEEL, 10 cm x 28 ga (0.36 mm) REF: CSK-TC10-3M,CSK Electrode, STAINLESS STEEL, 3M Cable, 10 cm x 28 ga (0.36 mm); REF: CSK-TC15, CSK Electrode, STAINLESS STEEL, 15 cm x 28 ga (0.36 mm); REF: CSK-TC15-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2332-2026·2026-06-17

    SporeTraq 12-test mail-in spore testing service used incorrect incubation

    The SporeTraq Mail-In Spore Testing Service, 12 tests, is being recalled because an incorrect incubation process was performed on the product.

    Product
    Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2331-2026·2026-06-17

    SporeTraq 52-test mail-in spore testing service used incorrect incubation

    The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.

    Product
    Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V390000·2026-06-15

    Forest River Recalls 2023-2024 XLR Toy Haulers for Incorrect Weight Rating

    Forest River is recalling 2023-2024 XLR Toy Hauler trailers because the listed Gross Vehicle Weight Rating exceeds the chassis rating, creating a risk of overloading and crashes.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V388000·2026-06-12

    2027 Thomas Built SAF-T-LINER HDX2 School Buses Recalled for Joint Strength

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER HDX2 school buses because front and mid-body interior joints may have insufficient strength, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V389000·2026-06-12

    Land Rover recalls vehicles over corroding driver airbag clockspring connectors

    Jaguar Land Rover is recalling certain 2020-2026 Defender, 2021-2026 Discovery and 2022-2026 Range Rover vehicles because the driver's air bag clockspring connector may corrode.

    Product
    LAND ROVER — LAND ROVER DEFENDER, DISCOVERY, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V385000·2026-06-12

    Winnebago Recalls 2026-2027 Revel Models Due to Incorrect Tire Label

    Winnebago is recalling 2026-2027 Revel and Revel Sport vehicles because the tire information label lists the wrong tire size, which could lead to incorrect replacements and increased crash risk.

    Product
    WINNEBAGO — WINNEBAGO REVEL SPORT, REVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E035000·2026-06-12

    Waymo Recalls 5th Generation Automated Driving Systems for Software Defect

    Waymo is recalling 5th Generation Automated Driving Systems because software may allow vehicles to enter closed freeway construction zones, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E034000·2026-06-12

    Marion Body Works Recalls Waltco Liftgates on Morgan Dry Vans

    Marion Body Works is recalling Waltco MDV series liftgates on Morgan aluminum dry vans because deck pins may break, causing the platform to fall.

    Product
    STRUCTURE:BODY:HATCHBACK/LIFTGATE:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V387000·2026-06-12

    Kawasaki Recalls 2025-2026 W230 Motorcycles Due to Turn Signal Defect

    Kawasaki is recalling 2025-2026 W230 motorcycles because defective turn signal bulbs may fail, increasing crash risk. Dealers will replace the lights free of charge.

    Product
    KAWASAKI — KAWASAKI W230
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26538·2026-06-11

    LiKee pull string teething toys reported to cause choking incidents

    About 24,400 LiKee Pull String teething toys are being recalled after ten reports of the silicone strings reaching the back of a child's throat, causing respiratory distress or choking.

    Product
    LiKee Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide