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.

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.

55226–55250 of 83431

  • SevereNHTSA·16V273000·2016-05-06

    Dodge Journey Recall for Power Steering Hose Rupture Risk

    Chrysler is recalling 2009-2016 Dodge Journey vehicles because the power steering return hose may rupture in cold weather, causing loss of steering assist.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·027-2016 expansion·2016-05-06

    Pilgrim's Pride Recalls Chicken Products Due to Possible Foreign Matter

    Pilgrim's Pride is recalling approximately 5.2 million pounds of fully cooked chicken products that may be contaminated with extraneous metal materials.

    Product
    Pilgrim's Pride Corporation — Pilgrim's Pride Corp. Recalls Poultry Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateNHTSA·16V274000·2016-05-06

    Land Rover Recalls Discovery Sport for License Plate Lamp Defect

    Land Rover is recalling 2015-2016 Discovery Sport vehicles because the license plate illumination lamp may fall out, making the vehicle difficult to identify at night.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1244-2016·2016-05-04

    Marathon Ventures Recalls Macadamia Nuts Due to Salmonella Contamination

    Marathon Ventures Inc. is recalling macadamia nuts under seven brands because FDA testing found Salmonella in a retail package.

    Product
    Macadamia Diced Nuts packaged under the following brands: 1) Shurfine, Item no. 86635, 5 OZ (142 g) plastic bags, packed 12 bags per case, UPC 0 15400 86635 4. Distributed by Western Family Foods, Inc., Portland OR. 2) Western Family, 5 OZ (142 g) plastic bags, packed 12…
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-1249-2016·2016-05-04

    Roland Fire Roasted Red Pepper Strips Recalled for Glass Fragments

    Roland Foods is recalling Fire Roasted Red Pepper Strips due to the possible presence of glass fragments in specific lots.

    Product
    Roland (R) Fire Roasted Red Pepper Strips, NET WT. 5 LB. 8 OZ. (2.5 kg), UPC 10041224456287 (carton) and 04122456280 (can), PRODUCT OF PERU -- Packed Exclusively For: ROLAND FOODS, LLC, New York, NY 10070
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V271000·2016-05-04

    Kaufman Trailers Recalls 2015-2016 Flatbed and Wedge Car Haulers

    Kaufman is recalling 2015-2016 Flatbed Equipment and Wedge Car Hauler trailers because axle hanger lock nuts may loosen, potentially causing the axle to detach and increasing crash risk.

    Product
    KAUFMAN — KAUFMAN WEDGE CAR HAULER, FLATBED EQUIPMENT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1127-2016·2016-05-04

    Organic Traditions Sprouted Chia & Flax Seed Powder Recalled for Salmonella Risk

    Health Matters America is recalling Organic Traditions Sprouted Chia & Flax Seed Powder due to potential Salmonella contamination.

    Product
    Organic traditions SPROUTED CHIA & FLAX SEED POWDER, NET WT. 8 oz./227g (UPC barcode 854260006216), and NET WT. 16oz./454g bag (UPC barcode 85426000547) --- The product is packed in a sealed flexible plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1580-2016·2016-05-04

    Hologic InPlex CF Molecular Test Recalled for False Positives and Leaking

    Hologic is recalling InPlex CF Molecular Tests due to false positive results and leaking cards, which could lead to unnecessary invasive testing during pregnancy.

    Product
    Hologic InPlex CF Molecular Test (IVD); Catalog Number: 95-432.
    Category
    Medical Device
    Distribution
    30 states
  • SevereNHTSA·16V270000·2016-05-04

    Newmar Recalls 2015-2016 Ventana Models Due to Front Sway Bar Defect

    Newmar is recalling 2015-2016 Ventana and Ventana LE vehicles because front sway bar brackets may not fit properly, risking bolt failure and loss of vehicle control.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·035-2016·2016-05-04

    Michael Angelo's Vegetable Lasagna Recalled for Undeclared Allergens

    Michael Angelo's is recalling 1,575 pounds of vegetable lasagna due to misbranding and undeclared turkey and eggs.

    Product
    Michael Angelo's Gourmet Foods Inc. — Michael Angelo's Gourmet Foods, Inc. Recalls Vegetable Lasagna Products Due To Misbranding And Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-1069-2016·2016-05-04

    WelleCo Super Elixir Greens Recalled for Potential Salmonella Contamination

    Welle Pty Ltd is recalling WelleCo Super Elixir Alkalising Greens pouches due to potential Salmonella contamination. The recall affects 150g and 300g pouches sold online in the U.S.

    Product
    The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net, 300g/10.6 oz net Fine Powder welleco.com
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Food)·F-1126-2016·2016-05-04

    Health Matters America Recalls Sprouted Flax Seed Powder for Salmonella Risk

    Health Matters America is recalling Organic Traditions Sprouted Flax Seed Powder due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Organic traditions SPROUTED FLAX SEED POWDER, NET WT. 8 oz/227g, UPC 854260006261 --- The product is packed in a sealed flexible plastic bag.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1583-2016·2016-05-04

    Mako Surgical Recalls RESTORIS PST RIO Offset Shell Impactor

    Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.

    Product
    RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2016·2016-05-04

    Research Instruments Recalls Integra 3 Micromanipulators Due to Faulty Power Cable

    Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.

    Product
    Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted Reproduction is used to accurately position microtools under a microscope for the techniques of Assisted Reproduction. The Rl Integra is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2016·2016-05-04

    NOW Foods Recalls Elderberry Supplements Due to Undeclared Soy Lecithin

    NOW Foods is recalling 57 bottles of Elderberry 500 mg capsules because they contain undeclared soy lecithin, a common allergen.

    Product
    Elderberry 500 mg packaged in a white and orange bottle containing 60 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-1554-2016·2016-05-04

    Horiba Recalls ABX Pentra 400 and C400 Clinical Chemistry Analyzers

    Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.

    Product
    Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1562-2016·2016-05-04

    GE Healthcare Aisys Anesthesia Machines Recalled for Suction Tubing Defect

    GE Medical Systems is recalling Aisys and Aisys CS2 anesthesia machines because kinked vacuum suction tubing may cause inadequate airway clearance and ventilation.

    Product
    GE Healthcare, Aisys and Aisys CS2. Intended to provide general inhalation anesthesia and ventilator support to a wide range of patients (neonatal, pediatric, and adult).
    Category
    Medical Device
    Distribution
    26 states
  • HighFDA (Devices)·Z-1559-2016·2016-05-04

    Becton Dickinson Recalls Listeria-Contaminated Trypticase Soy Agar Plates

    Becton Dickinson is recalling Trypticase Soy Agar and MacConkey II Agar plates contaminated with Listeria monocytogenes. The non-sterile media are used for growing and detecting bacteria.

    Product
    Trypticase TM Soy Agar with 5% Sheep Blood (TSA IITM) // MacConkey II Agar Cat. Number 221291, Lot Number 6034889, Exp. Date : April 20, 2016 Product is sold in cartons of 100 plates each. Product Usage: Trypticase Soy Agar with 5% Sheep Blood is used for the growth of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1553-2016·2016-05-04

    Horiba Recalls ABX Pentra 400 Analyzers Due to Malfunctions

    Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers because they malfunction when specific alarms appear on the system.

    Product
    ABX Pentra 400 (version 5.0.8 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1561-2016·2016-05-04

    Elekta Radionuclide Radiation Therapy System Recalled for Frame Adapter Latch Defect

    Elekta is recalling 217 Radionuclide Radiation Therapy Systems because frame adapter latches can lock without proper pin insertion, potentially compromising treatment accuracy.

    Product
    Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a few millimeters to several centimeters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1563-2016·2016-05-04

    3M Steri-Vac Gas Sterilizer Valves Recalled for Labeling Error

    3M is recalling 74 Steri-Vac Gas Sterilizer valves due to a labeling error that could cause incorrect installation and potential valve failure.

    Product
    3M Steri-Vac Gas Sterilizer/Aerator, models 5XL and 8XL.
    Category
    Medical Device
    Distribution
    15 states