The Recall Desk

State

Louisiana product recalls

73,824 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.

What the numbers show

Total
6,966
Critical
1,107
Severe
1,740
Most recent
2026-11-04

Of the 6,966 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 1,740 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47126–47150 of 80790

  • LowFDA (Devices)·Z-2316-2017·2017-06-14

    MedTest DX Assayed Human Multi Sera Control Recall for Out-of-Spec Values

    Medtest Holdings, Inc. is recalling MedTest DX Assayed Human Multi Sera Control Level 1 and Level 2 because control values are outside of specification.

    Product
    MedTest DX Assayed Human Multi Sera Control Level 1 (HNC200) and Level 2 (HEC200) HEC200 " Sml amber glass vial with rubber stopper and black plastic screw cap. " 1 0 control vials per box, 12 cell foam insert. HNC200 " Sml amber glass vials with rubber stopper and green…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0897-2017·2017-06-14

    Hetero USA Recalls Acyclovir Tablets Due to Human Hair Presence

    Hetero USA Inc. is recalling 13,692 bottles of Acyclovir 800 mg tablets because human hair was found melded into the tablets.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·070-2017·2017-06-13

    OFD Foods Recalls Beef Hash Due to Possible Rubber Contamination

    OFD Foods is recalling Mountain House freeze-dried beef hash due to possible rubber contamination. No illnesses have been reported.

    Product
    OFD Foods LLC — OFD Food, LLC. Recalls Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V376000·2017-06-13

    Dodge Grand Caravan Recalled for Air Bag Wiring Defect

    Chrysler is recalling 2011-2012 Dodge Grand Caravan vehicles because the driver's air bag wiring may chafe and short circuit, causing unexpected deployment.

    Product
    DODGE — DODGE GRAND CARAVAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17176·2017-06-13

    Trango Recalls Vergo Belay Devices Due to Fall and Injury Hazards

    Trango is recalling about 2,600 Vergo belay devices because the handle can loosen, causing the braking system to malfunction and posing fall hazards to climbers.

    Product
    Vergo belay devices (climbing tool)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17177·2017-06-13

    Noble House Recalls Dining Chairs Due to Leg Breakage and Fall Hazard

    Noble House is recalling about 3,300 dining chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.

    Product
    Dining chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·065-2017·2017-06-09

    Conagra Recalls Spaghetti and Meatball Products for Undeclared Milk Allergen

    Conagra Brands is recalling approximately 717,338 pounds of spaghetti and meatball products because they contain undeclared milk, a known allergen.

    Product
    Hometown Food Company — Conagra Brands, Inc. Recalls Spaghetti and Meatball Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·067-2017·2017-06-09

    Tyson Recalls Breaded Chicken Products Due to Undeclared Milk Allergen

    Tyson Foods is recalling approximately 2.5 million pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·068-2017·2017-06-09

    Gourmet Boutique Recalls Breaded Chicken Products Due to Undeclared Milk Allergen

    Gourmet Boutique LLC is recalling approximately 294,744 pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.

    Product
    Gourmet Boutique, LLC — Gourmet Boutique LLC Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V371000·2017-06-09

    Chrysler Recalls 2017 Pacifica Plug-In Hybrids for Inverter Defect

    Chrysler is recalling 2017 Pacifica Plug-In Hybrids because a power inverter defect may cause the vehicle to stop moving, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2017·2017-06-08

    Maid-Rite Recalls Beef Products Due to Undeclared Milk Allergen

    Maid-Rite Specialty Foods is recalling approximately 174,000 pounds of beef products because they contain undeclared milk, a known allergen.

    Product
    Maid-Rite Specialty Foods, Inc — Maid-Rite Specialty Foods, LLC. Recalls Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V369000·2017-06-08

    Supreme Signature Van and Kold King Recall for Rear Reflector Height

    Supreme is recalling 2007-2017 Signature Van and Kold King vehicles because rear reflex reflectors may be mounted too high, failing federal safety standards and increasing crash risk.

    Product
    SUPREME — SUPREME SIGNATURE VAN, KOLD KING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17175·2017-06-08

    GT Mountain Bicycles Recalled Due to Handlebar Crack Hazard

    Cycling Sports Group is recalling about 1,000 GT mountain bicycles because the handlebars can crack, posing a fall hazard to consumers.

    Product
    GT mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V368000·2017-06-07

    Porsche Recalls Panamera and Cayenne Models for Engine Stall Risk

    Porsche is recalling specific 2010-2012 Panamera and 2011 Cayenne vehicles because loose camshaft controllers may cause the engine to stall, increasing crash risk.

    Product
    PORSCHE — PORSCHE PANAMERA S, PANAMERA 4S, PANAMERA TURBO, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0877-2017·2017-06-07

    SCA Pharmaceuticals Recalls Cefazolin Sodium Bags Due to Leaking

    SCA Pharmaceuticals is recalling 70 bags of cefazolin sodium due to leaks at the seam, which compromises the product's sterility.

    Product
    ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 3g, Total Approximate Volume 115 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0524-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0879-2017·2017-06-07

    SCA Pharmaceuticals Recalls Phenylephrine Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 30 bags of Phenylephrine HCL injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    PHENYLephrine HCL in 0.9% Sodium Chloride injectable, 10 mg (Final Concentration = 0.1 mg per mL) Total Volume 100 mL, Single Dose Container bag, Preservative Free (Contains Sulfites), Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0810-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0871-2017·2017-06-07

    SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 56 bags of morphine sulfate in 0.9% Sodium Chloride injectable because the bags are leaking at the seam, compromising sterility.

    Product
    morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100 mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0870-2017·2017-06-07

    SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 80 bags of morphine sulfate injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0874-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injectable Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling fentanyl citrate injectable bags because they are leaking at the seam, which compromises sterility.

    Product
    fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable,20 mcg per mL, Single Dose Container bag, (Total fentanyl Dose 2,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-203-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0878-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Magnesium Sulfate Injectable Bags

    SCA Pharmaceuticals is recalling 40 bags of Magnesium Sulfate injectable solution due to seam leaks that compromise sterility.

    Product
    MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable, 4g, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0737-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0875-2017·2017-06-07

    SCA Pharmaceuticals Recalls Hydrocodone Injectable Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 87 bags of Hydromorphone HCL injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml, Total Volume 100mL, Single Dose Container bag, (Total HYDROmorphone Dose 20 mg per 100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0300-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Cefazolin Sodium Injectable Bags

    SCA Pharmaceuticals is recalling 240 bags of cefazolin sodium injectable due to seam leaks that compromise sterility.

    Product
    ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g, Total Approximate Volume 100 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0522-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0872-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Seam Leaks

    SCA Pharmaceuticals is recalling 118 bags of fentanyl injection due to seam leaks that compromise sterility. The product was distributed nationwide in the USA.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0229-32
    Category
    Drug
    Distribution
    Distributed nationwide