The Recall Desk

State

Indiana product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48276–48300 of 83422

  • HighFDA (Devices)·Z-2306-2017·2017-06-14

    Arrow International Recalls Two-Lumen Hemodialysis Catheterization Kits

    Arrow International Inc is recalling specific lots of two-lumen hemodialysis catheterization kits due to a Class II medical device recall.

    Product
    Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2297-2017·2017-06-14

    Pinnacle Foods Recalls Aunt Jemima Pancakes for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima 12 Pancakes Made with Whole Grain due to potential Listeria monocytogenes contamination. The recall covers 6,955 units distributed nationwide.

    Product
    AUNT JEMIMA(R) 12 PANCAKES MADE WITH WHOLE GRAIN, NET WT 14.5oz UPC 019600066408
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2310-2017·2017-06-14

    Pinnacle Foods Recalls Hilltop Hearth French Toast for Listeria Risk

    Pinnacle Foods is recalling Hilltop Hearth and Mrs. Butter-worth's French Toast nationwide due to a potential for Listeria monocytogenes contamination.

    Product
    French toast packaged as follows: a) Hilltop HEARTH, FRENCH TOAST, 18 8 COUNT BAGS, NET WT 10 LB 11.2 OZ, UPC 075810861816 b) Hilltop HEARTH, FRENCH TOAST, 12 6 COUNT BAGS, NET WT 10 LB 11.2 OZ, UPC 075810843855 c) Hilltop HEARTH FRENCH TOAST, 12 6 COUNT BAGS, NET WT. 10 LB…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2304-2017·2017-06-14

    Aunt Jemima Waffles Recalled for Potential Listeria Contamination

    Pinnacle Foods is recalling Aunt Jemima Buttermilk Waffles due to potential Listeria monocytogenes contamination. The recall covers 403,583 units distributed nationwide.

    Product
    AUNT JEMIMA(R) 14 BUTTERMILK WAFFLES, NET WT 17.18oz UPC 019600062103
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2249-2017·2017-06-14

    Alphatec Recalls Arsenal Spinal Fixation System Set Screws

    Alphatec Spine is recalling Arsenal Spinal Fixation System Set Screws due to a trend of postoperative disengagement from the screw body.

    Product
    Arsenal Spinal Fixation System, Set Screw, Part No. 47027 Product Usage: The Arsenal Spinal Fixation System is intended for posterior, non-cervical, spinal fixation as an adjunct to fusion for the treatment of degenerative disease, deformity, and trauma indications. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2306-2017·2017-06-14

    Aunt Jemima Low Fat Waffles Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima 14 Low Fat Waffles nationwide due to potential Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) 14 LOW FAT WAFFLES, NET WT 17.18oz UPC 019600062301
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2295-2017·2017-06-14

    Aunt Jemima Blueberry Pancakes Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima 12 Blueberry Pancakes nationwide due to potential Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) 12 BLUEBERRY PANCAKES, NET WT 14.8oz UPC 019600064701
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2263-2017·2017-06-14

    Arrow Central Venous Catheter Kit Recalled for Needlestick Injury Risk

    Arrow International is recalling 43,394 units of ARROWg+ard Blue PLUS Two-Lumen Central Venous Catheterization Kits due to safety cover disengagement and needlestick injury reports.

    Product
    ARROWg+ard Blue PLUS(R) Two-Lumen Central Venous Catheterization Kit. The Arrow(r) CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to: multiple infusions…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2293-2017·2017-06-14

    Pinnacle Foods Recalls Aunt Jemima Mini Pancakes Due to Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Lil' Griddles Mini pancakes nationwide due to a potential for Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) LIL' GRiDDLES(TM) MINI pancakes, 40 COUNT, NET WT 14.5oz UPC 019600054801
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2303-2017·2017-06-14

    Pinnacle Foods Recalls Aunt Jemima Waffles Due to Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Homestyle Waffles nationwide due to a potential for Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) 14 HOMESTYLE WAFFLES, NET WT 17.18oz UPC 019600062004
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2305-2017·2017-06-14

    Aunt Jemima Blueberry Waffles Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima 14 Blueberry Waffles due to potential Listeria monocytogenes contamination. The recall covers 153,513 units distributed nationwide.

    Product
    AUNT JEMIMA(R) 14 BLUEBERRY WAFFLES, NET WT 17.18oz UPC 019600062202
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2309-2017·2017-06-14

    Aunt Jemima Mini Cinnamon Roll Pancakes Recalled for Listeria Risk

    Pinnacle Foods is recalling Aunt Jemima Mini Cinnamon Roll Pancakes due to a potential for Listeria monocytogenes contamination.

    Product
    AUNT JEMIMA(R) MiNi pancakes, CINNAMON ROLL, NET WT 3.2 OZ, UPC 001960043568
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0892-2017·2017-06-14

    Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations

    Qualgen is recalling Estradiol 18 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 6,361 pellets distributed nationwide.

    Product
    Estradiol 18 mg pellet , 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, Subcutaneous Use Only, Rx Only, Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC: 69761-018-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0881-2017·2017-06-14

    Spectrum Laboratory Estradiol API Recalled for CGMP Deviations

    Spectrum Laboratory Products is recalling Estradiol active pharmaceutical ingredient due to Good Manufacturing Practice deviations found during an FDA inspection.

    Product
    Estradiol (17-B-Estradiol; Estra-1,3,5(10)-triene-3, 17B-diol; Oestradiol) Plant Base, Micronized, U.S.P active pharmaceutical ingredient, packaged in 1g, 5g, 25g, 6 x 25g, and 100g containers, Rx only, Spectrum Chemical Mfg. Corp, Gardena, CA 90248, New Brunswick, NJ 08901…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0885-2017·2017-06-14

    Dr. Reddy's Recalls Zenatane Isotretinoin Capsules for Dissolution Failures

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications, potentially affecting drug absorption.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2314-2017·2017-06-14

    Cook Medical Recalls LapSac Introducers Due to Inadequate Reprocessing Instructions

    Cook Medical is voluntarily recalling LapSac Introducers because the reprocessing instructions do not provide sufficient detailed information for cleaning, disinfection, and sterilization.

    Product
    LapSac Introducer, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to aid in the introduction of a LapSac during endoscopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0883-2017·2017-06-14

    Dr. Reddy's Recalls Zenatane Isotretinoin Capsules for Dissolution Failures

    Dr. Reddy's Laboratories is recalling Zenatane (isotretinoin) capsules because some lots failed to meet dissolution specifications, potentially affecting drug absorption.

    Product
    ZENATANE — ZENATANE (ISOTRETINOIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2313-2017·2017-06-14

    Cook Medical Recalls Endoscopic Curved Needles Due to Reprocessing Instruction Deficiencies

    Cook Medical is voluntarily recalling 725 units of endoscopic curved needles because the reprocessing instructions do not provide sufficient detail for proper cleaning and sterilization.

    Product
    Endoscopic Curved Needle, Surgical Needle Guide, Supplied sterilized by ethylene oxide gas in peel-open packages. Used for internal suturing under direct vision during intraabdominal endoscopic procedures. The needle driver design affords precise placement and control of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2307-2017·2017-06-14

    Arrow International Recalls Hemodialysis Catheterization Kits

    Arrow International Inc is recalling specific hemodialysis catheterization kits due to a lack of clinical data supporting the antimicrobial surface's effectiveness in preventing infections.

    Product
    ARROWg+ard Blue You-Bend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The Arrow(r) CVC is indicated to provide short-term ( < 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2310-2017·2017-06-14

    Cook Medical Recalls Willscher Vas Reapproximator Sets Due to Reprocessing Instructions

    Cook Medical is voluntarily recalling Willscher Vas Reapproximator Sets because the reprocessing instructions lack sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    Willscher Vas Reapproximator Set, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2017·2017-06-14

    Iba Dosimetry Recalls Large Stealth Chamber Dosimeters for Measurement Deviations

    Iba Dosimetry is recalling 110 Large Stealth Chambers because they may show measurement deviations and geometric shadowing when used as reference detectors.

    Product
    Large Stealth Chamber, Catalog Numbers: DS50-001-XL-T, DS50-002-XL-T, DS50-003-XL-T, DS50-102-XL-T, DS50-103-XL-T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2311-2017·2017-06-14

    Cook Medical Recalls Willscher Vas Skewers Due to Insufficient Reprocessing Instructions

    Cook Medical is voluntarily recalling Willscher Vas Skewers because the provided instructions do not contain sufficient detail for proper cleaning, disinfection, and sterilization.

    Product
    Willscher Vas Skewers, Surgical Instrument, Supplied sterilized by ethylene oxide gas in peel-open packages. Used to stabilize the vas ends during microscopic vasovasostomy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0889-2017·2017-06-14

    Qualgen Recalls Estradiol Pellets Due to Quality Assurance Deviations

    Qualgen is recalling Estradiol 25 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 1,153 pellets distributed nationwide.

    Product
    Estradiol 25 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF, in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only. Rx Only ,Manufactured by: Qualgen 14844 Bristol Park Blvd Edmond, OK 73013 NDC 69761-025-01,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0896-2017·2017-06-14

    Qualgen Estradiol Pellets Recalled for Quality Assurance Deviations

    Qualgen is recalling Estradiol 6 mg pellets due to CGMP deviations and lack of quality assurance. The recall covers 4,815 pellets distributed nationwide.

    Product
    Estradiol 6 mg pellet 99.5% Estradiol USP, .5% Stearic Acid NF in 1 count, 12 count, and 30 count bottles, Sterile Office Use Only, For Subcutaneous Use Only Rx Only, Manufactured by; Qualgen 14844 Bristol Park Blvd. Edmond, OK 73013 NDC: 69761-006-01.
    Category
    Drug
    Distribution
    Distributed nationwide