The Recall Desk

State

Louisiana product recalls

73,738 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,965
Critical
1,107
Severe
1,739
Most recent
2026-10-28

Of the 6,965 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,739 (25%) are Severe.

These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35551–35575 of 80703

  • SevereNHTSA·19V606000·2019-08-16

    Kenworth T270 and T370 Recalled for Brake Hose Separation Risk

    PACCAR is recalling 2020 Kenworth T270 and T370 trucks because loose fittings may cause the brake air hose to separate, reducing braking ability.

    Product
    KENWORTH — KENWORTH T270, T370
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V604000·2019-08-16

    Forest River Recalls 2019 Rockport Vans Due to Welding Defect

    Forest River is recalling 2019 Rockport box vans and service bodies because improperly welded bulk storage beams may fail when loaded, posing an injury risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V605000·2019-08-16

    Mercedes-Benz Recalls 2019 CLS 450 for Electrical Wiring Defect

    Mercedes-Benz is recalling 2019 CLS 450 vehicles because an electrical line may chafe, causing engine stalls or electrical system failures that increase crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·084-2019·2019-08-15

    Tyson Recalls Weaver Chicken Patties Due to Foreign Matter Contamination

    Tyson Foods is recalling approximately 39,078 pounds of Weaver brand frozen chicken patties due to possible foreign matter contamination. Consumers should not consume these products.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Weaver Brand Ready-To-Eat Chicken Patty Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E054000·2019-08-15

    Capco Recalls CTR Outer Tie Rods Due to Durability Concerns

    Capco USA is recalling CTR Outer Tie Rods because the taper on the ball studs may affect durability. This defect could impact vehicle control and increase crash risk.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V602000·2019-08-15

    Altec Recalls Aerial Devices Due to Winch Valve Defect

    Altec is recalling 2012-2019 aerial devices because a winch valve defect may allow lifting beyond rated capacity, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V603000·2019-08-15

    Land Rover Recalls 2018 Range Rovers for Backup Camera Software Defect

    Jaguar Land Rover is recalling 2018 Range Rover and Range Rover Sport vehicles because the backup camera may fail to display the rearview image, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1978-2019·2019-08-14

    Shirakiku Fish Cake Age Balls Recalled for Undeclared Allergens

    Wismettac Asian Foods is recalling Shirakiku Fish Cake Age Balls because they may contain undeclared egg, milk, and shellfish.

    Product
    Shirakiku FISH CAKE AGE BALL SK F; 20/ 150G; Net Wt. 5.29 oz. Keep Frozen, 15 pcs. UPC 074410925574 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
    Category
    Food
    Distribution
    38 states
  • CriticalFDA (Food)·F-1979-2019·2019-08-14

    Shirakiku Fish Cake Recalled for Undeclared Allergens

    Wismettac Asian Foods is recalling Shirakiku Fish Cake Satsuma Age due to possible undeclared egg, milk, and shellfish.

    Product
    Shirakiku FISH CAKE SATSUMA AGE SK F; 20/ 150G; Net Wt. 5.29 oz. Keep Frozen, 4 pcs. UPC 0744109925598 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
    Category
    Food
    Distribution
    38 states
  • CriticalFDA (Food)·F-1974-2019·2019-08-14

    Shirakuku Fish Cake Minch Balls Recalled for Undeclared Allergens

    Wismettac Asian Foods is recalling Shirakuku Fish Cake Minch Balls because they may contain undeclared egg, milk, and shellfish.

    Product
    Shirakuku FISH CAKE MINCH BALL SK F; 20/ 150G; Net Wt. 5.29 oz. Keep Frozen, 9 pcs. Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA UPC 074410925260
    Category
    Food
    Distribution
    38 states
  • CriticalFDA (Food)·F-1972-2019·2019-08-14

    Shirakiku Fish Cake Recalled for Undeclared Milk and Shellfish

    Wismettac Asian Foods is recalling Shirakiku Fish Cake due to possible undeclared milk and shellfish allergens.

    Product
    Shirakiku FISH CAKE IWASHI TEN SK F 20/150 g; Net WT. 5.29 oz. Keep frozen, 7 pcs. UPC 074410925246 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
    Category
    Food
    Distribution
    38 states
  • CriticalFDA (Food)·F-1976-2019·2019-08-14

    Shirakiku Fish Cake Recalled for Undeclared Egg, Milk, and Shellfish

    Wismettac Asian Foods is recalling Shirakiku Fish Cake Gobo Maki due to possible undeclared egg, milk, and shellfish.

    Product
    Shirakiku FISH CAKE GOBO MAKI SK F: 20/ 150G, Net Wt. 5.29 oz. Keep Frozen, 5 pcs. UPC 07441092550 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
    Category
    Food
    Distribution
    38 states
  • CriticalFDA (Food)·F-1977-2019·2019-08-14

    Shirakiku Fish Cake Recalled for Undeclared Egg, Milk, and Shellfish

    Wismettac Asian Foods is recalling Shirakiku Fish Cake Ika Maki due to possible undeclared egg, milk, and shellfish.

    Product
    Shirakiku FISH CAKE IKA MAKI SK F; 20/ 150G, Net Wt. 5.29 oz. Keep Frozen, 4 pcs. UPC 074410925567 Distributed by Wismettac Asian Foods, Inc. Santa Fe Springs, CA
    Category
    Food
    Distribution
    38 states
  • SevereFDA (Drugs)·D-1691-2019·2019-08-14

    RXQ Compounding Recalls Ondansetron Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Ondansetron 2 mg/mL Injection Solution because the product lacks assurance of sterility.

    Product
    ONDANSETRON 2 MG/ML INJECTION SOLUTION (PFV), 2 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0158-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2085-2019·2019-08-14

    Williams Original Chili Seasoning Recalled for Potential Salmonella Contamination

    CH Guenther & Sons, Inc. is recalling Williams Original Chili Seasoning because it contains cumin potentially contaminated with Salmonella.

    Product
    Williams Original Chili Seasoning, Net Wt. 1 OZ, Williams Foods, Inc. Lenexa, KS, UPC 0 41149 01100 7
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Drugs)·D-1668-2019·2019-08-14

    RXQ Compounding Recalls Inositol/Choline B12:B6 Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Inositol/Choline B12:B6 injection solution because there is a lack of assurance of sterility.

    Product
    Inositol/Choline B12:B6, 50/50/1/0.175 MG/ML INJ SOLN(Sulfa Free Lipostat), 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0999-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2073-2019·2019-08-14

    St Jude Medical Recalls 21 Ellipse DR Implantable Cardioverter Defibrillators

    St Jude Medical is recalling 21 Ellipse DR implantable cardioverter defibrillators due to damaged aluminum wires that may prevent the delivery of high-voltage therapy.

    Product
    ELLIPSE DR, REF: CD2377-36QC Implantable cardioverter defibrillators (ICDs)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1666-2019·2019-08-14

    RXQ Compounding Recalls Hydroxocobalamin Injections Due to Sterility Concerns

    RXQ Compounding LLC is recalling Hydroxocobalamin 1000 mcg/mL injections because the product lacks assurance of sterility. The recall covers all lots within expiry distributed nationwide.

    Product
    HYDROXOCOBALAMIN 1000 MCG/ML (PFV), 10 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0949-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1704-2019·2019-08-14

    RXQ Compounding Recalls Sodium Bicarbonate Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Sodium Bicarbonate 8.4% Injection due to a lack of assurance of sterility. The product is distributed nationwide.

    Product
    SODIUM BICARBONATE 8.4% (1 MEQ/ML) INJ SOLN (PFV), 50 ML PER VIAL, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0957-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1680-2019·2019-08-14

    RXQ Compounding Recalls MIC Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling MIC (Methionine/Inositol/Choline Chloride) 25/50/50 mg/mL Injection due to a lack of assurance of sterility.

    Product
    MIC (METHIONINE/INOSITOL/CHOLINE CHLORIDE) 25/50/50 MG/ML INJ, 30 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0100-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1638-2019·2019-08-14

    RXQ Compounding Recalls Buffered Lidocaine Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Buffered Lidocaine 1%+Epi 1:100,000 Injection Solution because the product lacks assurance of sterility.

    Product
    BUFFERED LIDOCAINE 1%+EPI 1:100,000 INJ SOL, [3ML NDC: 70731-0137-03 and 30ML NDC: 70731-0137-30] per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0137-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2074-2019·2019-08-14

    St Jude Medical Recalls 15 Ellipse DR Cardioverter Defibrillators

    St Jude Medical is recalling 15 Ellipse DR cardioverter defibrillators due to damaged aluminum wires that may prevent high-voltage therapy delivery.

    Product
    ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36C, UDI: 05414734507585
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1673-2019·2019-08-14

    RXQ Compounding Recalls Magnesium, Calcium, and Zinc Vials for Sterility Concerns

    RXQ Compounding LLC is recalling magnesium, calcium, and zinc vials due to a lack of assurance of sterility. The products were distributed nationwide.

    Product
    MAGNESIUM 200 MG/ML/ CALCIUM GLUC 6MG/ML/ ZINC 1MG/ML, 5ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0176-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1649-2019·2019-08-14

    RXQ Compounding Recalls DMPS Injection Due to Sterility Concerns

    RXQ Compounding LLC is recalling Dimercapto-Propanesulfonic 5% (DMPS) injection solution because the product lacks assurance of sterility.

    Product
    DIMERCAPTO-PROPANESULFONIC 5% (DMPS)( (PFV) INJ SOL, 5 ML per vial, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0904-05
    Category
    Drug
    Distribution
    Distributed nationwide