The Recall Desk

State

Indiana product recalls

73,833 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,598
Critical
1,908
Severe
2,536
Most recent
2026-11-04

Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54101–54125 of 83431

  • CriticalFDA (Drugs)·D-1137-2016·2016-07-13

    Hospira Recalls Magnesium Sulfate Injection Due to Particulate Matter

    Hospira Inc. is recalling specific lots of Magnesium Sulfate Injection due to confirmed particulate matter. The recall covers 88,500 vials distributed in the US and several Middle Eastern countries.

    Product
    Magnesium Sulfate Inj., USP 50%, 10 g/20 mL (0.5 g/mL), (4 mEq Magnesium/mL, 20 mL Single-dose vial, packaged in 25 vials per box, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-2168-02, barcode (01) 2 030409 216802 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1141-2016·2016-07-13

    Bee Extremely Amazed LLC Recalls Infinity Capsules Tainted With Sibutramine

    Bee Extremely Amazed LLC is recalling Infinity Capsules because the product was found to contain undeclared sibutramine, a withdrawn appetite suppressant.

    Product
    Infinity Capsules, 500 mg, 30-count bottle, Manufactured for Floyd Nutrition
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1661-2016·2016-07-13

    Pictsweet Vegetables for Cajun Gumbo Recalled for Listeria Risk

    The Pictsweet Company is recalling Vegetables for Cajun Gumbo because the onions used in the product may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Vegetables for Cajun Gumbo, Seasoned with a blend of Cajun Spices, NET WT 12 OZ (340g), UPC 70560 95818, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1657-2016·2016-07-13

    Kroger Vegetable Stir Fry Starters Recalled for Listeria Risk

    The Pictsweet Company is recalling Kroger Vegetable Stir Fry Starters because the onions used in the product may be contaminated with Listeria monocytogenes.

    Product
    Kroger(R) VEGETABLES WITH NOODLES, egg noodles, broccoli, carrots, green bell peppers, mushrooms, onions & red bell peppers, STIR FRY STARTERS(R), NET WT 12 OZ (340g), UPC 11110 89776, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1148-2016·2016-07-13

    FDA Recalls Ultimate Formula Capsules Tainted With Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling Ultimate Formula Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    Ultimate Formula Capsules, 250mg, 48-count bottles, Manufactured for: Zi Xiu Tang Success, LLC Trexlertown, PA 18087, USA www.zixiutangsuccess.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1154-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 42 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL Citrate 1 MCG/mL in 0.9% Sodium Chloride Injection, in 3 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992131
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1147-2016·2016-07-13

    SLIM TRIM U Capsules Recalled for Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling SLIM TRIM U Capsules because they contain undeclared sibutramine, a withdrawn drug.

    Product
    SLIM TRIM U Capsules, 250mg, 60-count bottles, Manufactured for Floyd Nutrition
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1157-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 148 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL CITRATE 4 MCG/mL in 0.9% SODIUM CHLORIDE Injection, in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999993491
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1165-2016·2016-07-13

    FDA Recalls Zero Xtreme Fat Burner for Unapproved Ingredients

    The FDA is recalling Zero Xtreme High Performance Fat Burner capsules because testing found unapproved ingredients. Consumers should stop using the product.

    Product
    Zero Xtreme High Performance Fat Burner capsules, 30-count bottle, Distributed by Xtreme Z Distributors, Inc., Miami, FL 33180
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1138-2016·2016-07-13

    Asset BOLD Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Asset BOLD Capsules because they contain undeclared sibutramine and phenolphthalein, making them unapproved drugs.

    Product
    Asset BOLD Capsules, 500 mg, 60-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1142-2016·2016-07-13

    Jenesis Capsules Recalled for Undeclared Sibutramine and Phenolphthalein

    Bee Extremely Amazed LLC is recalling Jenesis Capsules marketed as a dietary supplement because they contain undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.

    Product
    Jenesis Capsules, 350 mg, 60-count bottles, Manufactured for Timeless Solutions 1810 E. Sahara Ave #100 Las Vegas, Nevada 89104
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1150-2016·2016-07-13

    XCEL Advanced Capsules Recalled for Undeclared Phenolphthalein

    Bee Extremely Amazed LLC is recalling XCEL Advanced Capsules because they contain undeclared phenolphthalein, a withdrawn ingredient with carcinogenic concerns.

    Product
    XCEL ADVANCED Capsules, 350mg, 60-count bottles, Manufactured for JNS Health
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1139-2016·2016-07-13

    Asset extreme+PLUS Capsules Recalled for Undeclared Sibutramine

    Bee Extremely Amazed LLC is recalling Asset extreme+PLUS Capsules because the product was found to contain undeclared sibutramine, a withdrawn appetite suppressant.

    Product
    Asset extreme+PLUS Capsules, 500 mg, 30-count bottles, Distributed by Descor, LLC www.assetcapsules4u.com www.allnaturalbeelievers.com
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1158-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Syringes Nationwide

    Cantrell Drug Company is recalling 1,652 syringes of fentanyl citrate because the medication was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL Citrate 50 mcg/mL in Sterile Water for Injection, packaged in 2 mL syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-074-16, UPC: 0100352533074165
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1140-2016·2016-07-13

    Bee Pollen Capsules Recalled for Undeclared Withdrawn Drug Ingredients

    Bee Extremely Amazed LLC is recalling EVOLVE BEE POLLEN Capsules nationwide because they contain undeclared sibutramine and phenolphthalein, both withdrawn from the US market for safety reasons.

    Product
    EVOLVE BEE POLLEN Capsules, 250mg, 60-count bottles, Manufactured for 2637 E. Atlantic Blvd, Pompano Beach, Florida, 33062 WWW.BEEEXTREMELYAMAZED.COM
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1656-2016·2016-07-13

    Kroger Cajun Style Mirepoix Blend Recalled for Listeria Risk

    The Pictsweet Company is recalling Kroger Cajun Style Mirepoix Blend due to possible Listeria monocytogenes contamination in the onions.

    Product
    Kroger(R) CAJUN STYLE MIREPOIX BLEND, onions, celery, and green bell peppers, RECIPE BEGINNINGS(R), NET WT 12 OZ (340g), UPC 11110 89787, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1146-2016·2016-07-13

    FDA Recalls SlimeX-15 Capsules Containing Undeclared Sibutramine

    The FDA is recalling SlimeX-15 Capsules because they contain undeclared sibutramine, a withdrawn drug. Consumers should stop using the product.

    Product
    SlimeX-15 Capsules, 15 mg, 30-count bottles, Marketed by: Signature Pharmaceuticals Ltd. MUMBAI-400-030 Manufactured in India by: HAB Pharmaceuticals & Research Limited 10-Pharma City, SIDCUL, Selaqui, Dehradun, 248 197
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1162-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Midazolam HCl Injection Syringes

    Cantrell Drug Company is recalling 3,853 syringes of Midazolam HCl injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    Midazolam HCl in 0.9% Sodium Chloride Injection, 0.5 mg/mL 1 mL (0.5 mg/mL), 1 mL syringes, Rx Only, Cantrell Drug Co., Little Rock AR --- NDC 52533-157-45, UPC: 0100352533157455
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1655-2016·2016-07-13

    Pictsweet Recalls Frozen Chopped Onions for Listeria Risk

    The Pictsweet Company is recalling specific lots of frozen chopped onions due to possible Listeria monocytogenes contamination. The recall affects Kroger and Pictsweet brands distributed nationwide.

    Product
    Frozen chopped onions labeled as: a) Kroger(R) CHOPPED ONIONS, RECIPE BEGINNINGS(R), NET WT 12 OZ (340g), UPC 11110 89791, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202 b) PICTSWEET(R) Chopped Onions, recipe helper, NET WT 10 OZ (283g), UPC 70560 96609…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1152-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 884 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL citrate in 0.9% Sodium Chloride Injection, 10 mcg/1 mL (10 mcg/mL), in 1 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-024-45, UPC: 0100352533024450
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1660-2016·2016-07-13

    Pictsweet Frozen Seasoning Blend Recalled for Listeria Risk

    The Pictsweet Company is recalling specific lots of frozen seasoning blends due to potential Listeria monocytogenes contamination in the onion ingredients.

    Product
    Frozen seasoning blend labeled as: a) PICTSWEET(R) Seasoning Blend, recipe helper, NET WT 10 OZ (283g), UPC 70560 96902, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006 b) PICTSWEET(R) Seasoning Blend, NET WT 24 OZ (1 LB 8 OZ) 680g, UPC 70560 96911, DISTRIBUTED BY…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1156-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling fentanyl citrate injection syringes because they contain less active drug than labeled.

    Product
    fentaNYL citrate in 0.9% Sodium Chloride Injection, 5 mcg/1 mL (5 mcg/mL), in a) 1 mL syringe (NDC 52533-214-45, UPC: 0100352533214455) and b) 3 mL syringe (NDC 52533-214-60, UPC: 0100352533214608), Rx Only, Cantrell Drug Co., Little Rock, AR
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1663-2016·2016-07-13

    Pictsweet Steam'ables Summer Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Steam'ables Seasoned Summer Vegetables because they contain onions that may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Steam'ables, Seasoned Summer Vegetables, with Cracked Pepper Seasoning, NET WT 10 OZ (283g), UPC 70560 98001, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1659-2016·2016-07-13

    Pictsweet Steamables Spring Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Pictsweet Steamables Seasoned Spring Vegetables because the onions used in the product were recalled for possible Listeria monocytogenes contamination.

    Product
    PICTSWEET(R) Steamables, Seasoned Spring Vegetables, with Asparagus and Ground Peppercorn Seasoning, NET WT 10 OZ (283g), UPC 70560 97826, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide