The Recall Desk

State

Indiana product recalls

73,388 recalls have nationwide distribution and so reach Indiana. 9,587 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,587
Critical
1,913
Severe
2,528
Most recent
2026-09-30

Of the 9,587 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23101–23125 of 82975

  • HighFDA (Drugs)·D-0769-2022·2022-04-20

    Lansoprazole Delayed-Release Capsules Recalled for Out-of-Specification Dissolution

    Preferred Pharmaceuticals is recalling certain lots of Lansoprazole Delayed-Release Capsules 15mg due to dissolution testing results that do not meet specifications. Approximately 791 bottles were distributed nationwide.

    Product
    Preferred Pharmaceuticals, Inc. The Physician's Solution., Lansoprazole Delayed-Release Capsules, 15mg, Generic for Prevacid, 90-Count Bottle, Manufacturer: Dr Reddy's Laboratories Limited, NDC 68788-6390-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0924-2022·2022-04-20

    Abbott INDEFLATOR Plus 30 Device Recalled for Leaks and Connection Faults

    Abbott Vascular is recalling INDEFLATOR Plus 30 balloon inflators due to increasing complaints of leaks and intermittent loose connections that could affect device function during medical procedures.

    Product
    INDEFLATOR Plus 30 - REF 1000183 WPL2122277-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0996-2022·2022-04-20

    SKIPPY Reduced Fat Chunky Peanut Butter recalled for potential steel contamination

    Skippy Foods recalls SKIPPY Reduced Fat Chunky Peanut Butter due to potential small steel contaminants. The recall affects 9,353 cases distributed across multiple U.S. states.

    Product
    SKIPPY Reduced Fat Chunky Peanut Butter NET WT 16.3 oz (1 LB 3 OZ) 462 g UPC 037600104999 packaged in clear plastic jar with blue label
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0905-2022·2022-04-20

    Breast Milk Analyzer Lacks FDA Validation, Risks Sub-optimal Infant Nutrition

    Stanbio Laboratory's Creamatocrit Plus breast milk analyzer was marketed without required FDA 510(k) clearance. Its performance has not been validated, and erroneous results could lead to inadequate nutritional supplementation for infants.

    Product
    Separation Technology Creamatocrit Plus, Catalog Number: 100-146
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0993-2022·2022-04-20

    Taylor Farms Thai Noodle Salad Kit Recalled for Plexiglass Contamination

    Taylor Farms is recalling Thai Noodle Salad Kit (108 oz) due to plexiglass found in an ingredient. The affected product was distributed to Kroger locations in Illinois, Indiana, Kentucky, Missouri, and Ohio with best by dates March 10-16, 2022.

    Product
    Taylor Farms - Thai Noodle Salad Kit packaged in 108oz plastic bag *Product packages all salad ingredients separate then ships to retail location. Deli counter at retail location mix ingredients and sale as per order servings.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0942-2022·2022-04-20

    ARIA Radiation Therapy Management Software May Cause Treatment Location Error

    Varian ARIA radiation therapy management software versions 13.6 through 16.1 may generate incorrect treatment plan values that could direct radiation therapy to the wrong location. No illnesses have been reported.

    Product
    ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0938-2022·2022-04-20

    Pre-wired ECG Electrode Set Fails Defibrillation Voltage Safety Standard

    Graphic Controls' CLARAVUE Pre-wired Electrode set does not meet required electrical specifications for defibrillation use. The device fails to withstand 5,000 volts without breakdown, potentially resulting in ineffective defibrillation.

    Product
    CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779 50602-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0925-2022·2022-04-20

    Abbott Vascular Plus 30 Priority Pack Recalled for Connection Leaks

    Abbott Vascular is recalling seven lots of the Plus 30 Priority Pack due to increased reports of leaks and intermittent loose connections in the vascular devices.

    Product
    Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0913-2022·2022-04-20

    Hammertoe Correction Surgical System Recalled for Driver Connection Defect

    Nextremity Solutions recalls the Nextra Hammertoe Correction System because the driver's proximal end is oversized, making it difficult to connect and remove from the implant, potentially delaying surgery.

    Product
    Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0989-2022·2022-04-20

    Cinnamon Crumb Cake Recalled for Potential Foreign Materials

    Continental Mills voluntarily recalls Krusteaz Cinnamon Crumb Cake (Lot KX2063) due to potential foreign materials that could pose a choking or injury risk.

    Product
    Item # 722-0105, Krusteaz Cinnamon Crumb Cake. Product is shelf stable and packaged in a box. net wt. 21 oz., UPC 0 41449 11140 7.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0937-2022·2022-04-20

    CLARAVUE Pre-wired Electrode fails to meet electrical safety specification

    Graphic Controls' CLARAVUE Pre-wired Electrode units fail to meet electrical safety specifications required for defibrillation. The device delivers an inefficient electrical charge and may result in ineffective defibrillation.

    Product
    CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0997-2022·2022-04-20

    SKIPPY Creamy Peanut Butter recalled for potential steel contamination

    Skippy Foods recalls SKIPPY Creamy Peanut Butter Blended with Plant Protein (397g) due to potential small steel contaminants. The recall affects over 9,300 cases distributed across multiple states.

    Product
    SKIPPY Creamy Peanut Butter Blended with Plant Protein NET WT 14 (397 g) UPC 037600880954 packaged in clear plastic jar with black label
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-0929-2022·2022-04-20

    Siemens Atellica CH Hemoglobin A1c Reagent Kits Recalled for Quality Control Issues

    Siemens Healthcare is recalling Atellica CH Hemoglobin A1c reagent kits due to potential reagent carryover affecting quality control and patient test results. The issue may cause inaccurate diabetes monitoring measurements.

    Product
    Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H), Siemens Material Number 11097536
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0911-2022·2022-04-20

    Nextra Hammertoe Correction System surgical instruments recalled for defective connector

    Nextremity Solutions recalls 459 units of the Nextra Hammertoe Correction System due to an oversized proximal driver end that prevents proper connection and removal during surgery.

    Product
    Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0984-2022·2022-04-20

    Great Value Buttermilk Pancake Mix Recalled for Foreign Materials

    Continental Mills is recalling Great Value Buttermilk Pancake & Waffle Mix (item #714-5000) due to foreign materials. Approximately 1,125 cases were distributed nationwide.

    Product
    Item # 714-5000, Great Value Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 32 oz., UPC 0 78742 37082 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0766-2022·2022-04-20

    Cyanocobalamin Injection Recalled for Subpotent Drug - Out of Specification Assay

    Aurobindo Pharma USA Inc. is recalling 433,809 vials of Cyanocobalamin injection nationwide because assay testing showed the drug is subpotent, containing less than the specified 1,000 mcg/mL of active ingredient. Affected lots with specific expiration dates from September 2022 to April 2023 are identified for recall.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0926-2022·2022-04-20

    Philips Autoclavable Temperature Probes: Updated Cleaning Instructions

    Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.

    Product
    The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1000-2022·2022-04-20

    Dietary Supplement Recalled for Undeclared New Ingredient

    Bio-Botanica is recalling NATURE's ANSWER Coral Calcium supplements because the product contained cesium chloride, a New Dietary Ingredient. The recall affects 6852 bottles distributed to 17 states.

    Product
    NATURE's ANSWER Coral Calcium; Antioxidant Benefits*; 1000mg Coral Calcium per serving; DIETARY SUPPLEMENT; 90 capsules
    Category
    Drug
    Distribution
    17 states
  • ModerateFDA (Food)·F-0988-2022·2022-04-20

    Krusteaz Belgian Waffle Mix recalled due to foreign materials contamination

    Continental Mills voluntarily recalled 450 cases of Krusteaz Belgian Waffle Mix nationwide due to the presence of foreign materials.

    Product
    Item # 721-1000, Krusteaz Belgian Waffle Mix. Product is shelf stable and packaged in a box. net wt. 28 oz., UPC 0 41449 00186 9.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0930-2022·2022-04-20

    Siemens Atellica CH Fructosamine Reagent Recalled for Potential Carryover

    Siemens Healthcare Diagnostics is recalling Atellica CH Fructosamine reagent (lots 211359, 211451) due to potential reagent carryover that could affect diagnostic test accuracy.

    Product
    Atellica CH Fructosamine (Fruc), Siemens Material Number 11097637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0917-2022·2022-04-20

    FDA Recalls Touch Screen Modules for IVUS Imaging Systems

    Volcano Corp is recalling MM-TSM touch screen modules used with IntraSight Integrated IVUS systems because they may crack or become damaged, potentially rendering the imaging equipment non-functional.

    Product
    MM-TSM (Touch Screen Module/Secondary Controller/Bedside Controller), Part Numbers: 300002018101, 300002018102, used with IntraSight Integrated (Part Number: 797403) IVUS systems
    Category
    Medical Device
    Distribution
    50 states
  • ModerateFDA (Devices)·Z-0932-2022·2022-04-20

    Hydroxybutyrate Test Kits Recalled Due to Improper Storage

    Medline's Hydroxybutyrate LiquiColor Tests are recalled due to improper storage that may cause delayed test results. The recall affects 45 units distributed across 16 U.S. states.

    Product
    Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
    Category
    Medical Device
    Distribution
    16 states
  • HighNHTSA·22E034000·2022-04-19

    Enerco Recalls LP Gas Quick Connector Fittings for Fire Risk

    Enerco is recalling specific Mr. Heater LP gas quick connector fittings because they may crack and leak gas, increasing the risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:LINES AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V265000·2022-04-19

    Maserati Recalls 2022 MC20 Vehicles Due to Brake Light Malfunction

    Maserati is recalling 2022 MC20 vehicles because faulty rear tail lights may cause brake lights to flicker, potentially confusing other drivers and increasing crash risk.

    Product
    MASERATI — MASERATI MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide