The Recall Desk

State

Louisiana product recalls

73,576 recalls have nationwide distribution and so reach Louisiana. 6,960 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,960
Critical
1,109
Severe
1,737
Most recent
2026-10-21

Of the 6,960 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 6,960 recalls whose distribution notice names Louisiana specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27001–27025 of 80536

  • HighFDA (Devices)·Z-1714-2021·2021-06-09

    Zavation Orthopedic Stylet Recalled for Inadequate Sterilization

    Zavation is recalling 56 units of 10 gauge direct unilateral stylets used in spinal procedures because products distributed as sterile may not have been adequately sterilized. Affected units were distributed nationwide.

    Product
    10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKbd. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1717-2021·2021-06-09

    Orthopedic spinal implants recalled due to inadequate sterilization

    Zavation is recalling 7 units of 11G DIRECT SINGLE spinal implants (lots 2001185 and 2001243) because products distributed as sterile may not have been adequately sterilized. The devices were distributed nationwide.

    Product
    11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) CODE: INTVMN-SCDK. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1743-2021·2021-06-09

    10G Direct Single Bone Access Kits recalled for sterilization failure

    Zavation's 10G Direct Single Bone Access Kits are being recalled because products distributed as sterile may not have been adequately sterilized, posing infection risk in orthopedic procedures.

    Product
    10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1773-2021·2021-06-09

    Change Healthcare Enterprise Viewer software defect affects image display settings

    A software defect in Change Healthcare Enterprise Viewer versions 2.0 and 2.1 prevents the display of image presentation styles. The viewer is used nationwide for displaying medical images.

    Product
    Change Healthcare Enterprise Viewer - Product Usage: intended to be used with off-the-shelf hardware for the 2D and 3D display of DICOM and non-DICOM medical images, reports, and multimedia content.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0649-2021·2021-06-09

    Genpak Bake n Show Muffin Trays Recalled for Foreign Objects

    Genpak is recalling Bake n Show Muffin Trays in three sizes due to the discovery of foreign objects in product packaging. The recall affects units distributed across multiple US states and Canada.

    Product
    Bake n Show¿ Muffin Tray 4 Cavity Large, Bake n Show¿ Muffin Tray 4 Cavity Large Shallow & Bake n Show¿ Muffin Tray 6 Cavity
    Category
    Consumer Product
    Distribution
    24 states
  • ModerateFDA (Food)·F-0651-2021·2021-06-09

    Genpak Bake n Show Cake Trays Recalled for Foreign Objects

    Genpak is recalling Bake n Show Round and Square Cake Trays due to the presence of foreign objects found in product packaging. The trays were distributed across multiple U.S. states and Canada.

    Product
    Bake n Show¿ Cake Tray Round & Bake n Show¿ Cake Tray Square
    Category
    Consumer Product
    Distribution
    24 states
  • ModerateFDA (Food)·F-0647-2021·2021-06-09

    Lipodrene With 25mg Ephedra Extract recalled for unapproved food additive

    Hi Tech Pharmaceuticals is recalling Lipodrene With 25mg Ephedra Extract because the product contains 1,4-dimethylamylamine (DMAA), an unapproved food additive.

    Product
    Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9
    Category
    Drug
    Distribution
    38 states
  • ModerateFDA (Devices)·Z-1695-2021·2021-06-09

    K2M Cascadia AN Interbody Implants Recalled for Mislabeled Dimensions

    K2M, Inc is recalling Cascadia AN Interbody Convex lumbar implants with mislabeled product dimensions. The affected sizes include 10x22x14mm, 10x28x14mm, and 10x22x15mm. No injuries have been reported.

    Product
    Cascadia AN Interbody Convex 10x22x14mm Catalog Number: 6101-2102214NC-G2 Lumbar implants are intervertebral body fusion devices indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft when used as anadjunct to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0652-2021·2021-06-09

    Genpak Bake n Show Oven Ready Food Trays recalled for foreign objects

    Genpak is recalling Bake n Show Oven Ready Food Trays (16 ounce) due to foreign objects found in the packaging. The affected product was distributed across multiple U.S. states and Canada.

    Product
    Bake n Show¿ Oven Ready Food Tray 16 ounce
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Food)·F-0648-2021·2021-06-09

    Genpak Bake n Show Angel Food Trays Recalled for Foreign Objects

    Genpak is recalling Bake n Show Angel Food Trays (8-inch and 8-inch shallow models) because foreign objects were found in the product packaging. Consumers should stop using affected trays.

    Product
    Bake n Show¿ Angel Food Tray 8 Inch & 8 inch shallow
    Category
    Consumer Product
    Distribution
    24 states
  • ModerateFDA (Drugs)·D-0600-2021·2021-06-09

    Micardis (Telmisartan) 80 mg Tablets Recall Due to Subpotency

    Boehringer Ingelheim Pharmaceuticals is recalling Micardis 80 mg tablets (Lot #860412, expiration September 2022) because the tablets contain less active ingredient than required. This is a voluntary Class II recall.

    Product
    Micardis Tablets, (telmisartan Tablets) 80 mg, 30 ct. per folding cartons, Rx only, NDC 0597-0041-37), Distributed by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877
    Category
    Drug
    Distribution
    11 states
  • ModerateFDA (Food)·F-0650-2021·2021-06-09

    Bake n Show Pizza Cookie Tray recalled for foreign objects

    Genpak is recalling Bake n Show Pizza Cookie Trays (12") because foreign objects were found in product packaging. The recall affects multiple states and Canada.

    Product
    Bake n Show¿ Pizza Cookie Tray 12"
    Category
    Food
    Distribution
    24 states
  • LowFDA (Drugs)·D-0601-2021·2021-06-09

    Thiamine HCl Injection Recall: Vials with Incorrect Lot Numbers

    Mylan Institutional LLC is recalling Thiamine Hydrochloride Injection USP 200 mg/2 mL due to vials labeled with incorrect lot numbers. The cartons contain the correct lot number 200906 but vials inside are labeled with lot number 200901.

    Product
    THIAMINE HYDROCHLORIDE — THIAMINE HYDROCHLORIDE (THIAMINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·21V435000·2021-06-08

    Land Rover Defender Recalled for Rear Light Assembly Failure Risk

    Jaguar Land Rover is recalling 2020-2022 Defender X vehicles with smoked rear lights because a voltage spike can cause turn signals and brake lights to fail.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V433000·2021-06-07

    Coach House Platinum Recalled for Potential Gas Leak in Cooking Stove

    Coach House is recalling 2021 Platinum vehicles because an overtightened bolt on the cooking stove may damage the seal, causing a gas leak that increases fire risk.

    Product
    COACH HOUSE — COACH HOUSE PLATINUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V432000·2021-06-07

    2022 Honda Odyssey Second-Row Seat Frames May Unlock Unexpectedly

    Honda is recalling 2022 Odyssey vehicles because second-row outboard seat frames have deformed locking mechanisms that may prevent them from locking into place. Unlocked seats could move unexpectedly, increasing injury risk.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V430000·2021-06-04

    Highland Ridge RV Recalls Trailers with Propane Regulator Defect

    Highland Ridge RV is recalling certain 2019-2021 fifth wheel and travel trailers because a propane regulator may fail, increasing fire risk.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW, HIGHLAND RIDGE TT OPEN RANGE, SILVERSTAR, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V426000·2021-06-04

    KZRV Sidewinder Recalled for Propane Regulator Fire Risk

    KZRV is recalling 2018-2019 Sidewinder RVs because a propane regulator may fail, increasing pressure and fire risk.

    Product
    KZRV — KZRV SIDEWINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V425000·2021-06-04

    Jayco travel trailers and fifth wheels recalled for propane regulator failure fire risk

    Jayco is recalling approximately 87,649 certain 2017-2021 travel trailers and fifth wheels with defective Winntec propane regulators that may fail and increase fire risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER, JAYCO FIFTH WHEEL EAGLE, WHITE HAWK, PINNACLE, OCTANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V431000·2021-06-04

    Starcraft RV Recalls Travel Trailers and Fifth Wheels Due to Propane Regulator Defect

    Starcraft RV is recalling specific 2017-2021 travel trailers and fifth wheels because a propane regulator may fail, increasing fire risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT, STARCRAFT RV FW AUTUMN RIDGE, AR-ONE MAXX, MOSSY OAK, AUTUMN RIDGE OUTFITTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V429000·2021-06-04

    Trails West Sierra Trailer Recall for Gas Leak Risk

    Trails West is recalling one 2020 Sierra 4H 15x19 LQ trailer due to a potential gas leak from the stove that could increase fire risk.

    Product
    TRAILS WEST — TRAILS WEST SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V427000·2021-06-04

    Keystone Recalls 2019-2020 RVs Due to Propane Regulator Fire Risk

    Keystone is recalling 2019 Bullet and Sprinter and 2020 Hideout RVs because a propane regulator may fail, increasing fire risk.

    Product
    KEYSTONE — KEYSTONE HIDEOUT, BULLET, SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V428000·2021-06-04

    Recreational vehicles recalled for propane regulator failure and fire risk

    Heartland and Cruiser recreational vehicles with defective Winntec propane regulators may experience increased pressure, enlarging gas-appliance flames and increasing fire risk. Dealers will replace the regulator free of charge.

    Product
    HEARTLAND — HEARTLAND, CRUISER RV, CRUISER TRAIL RUNNER, LITHIUM, PROWLER, PIONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·21147·2021-06-03

    Fisher-Price Recalls Rock 'n Glide Soothers After Four Infant Deaths

    Fisher-Price is recalling 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders due to reports of four infant deaths from suffocation.

    Product
    Fisher-Price 4-in-1 Rock 'n Glide Soothers and 2-in-1 Soothe 'n Play Gliders
    Category
    Consumer Product
    Distribution
    Distributed nationwide