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.

55251–55275 of 83431

  • HighFDA (Devices)·Z-1558-2016·2016-05-04

    Siemens SOMATOM Force CT Systems Recalled for Image Artifacts

    Siemens is recalling 37 SOMATOM Force CT systems because a software error in the Neonate Head protocol may cause image artifacts, potentially leading to misdiagnosis.

    Product
    SOMATOM Force, Computed Tomography x-ray system intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1131-2016·2016-05-04

    NOW Foods Recalls Gingko Biloba Supplements Due to Undeclared Soy

    NOW Foods is recalling Gingko Biloba 60mg capsules because they contain undeclared soy lecithin. Consumers should stop using the product and return it to the place of purchase.

    Product
    Gingko Biloba 60mg packaged in a white and orange bottle containing 120 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·F-1133-2016·2016-05-04

    NOW Foods Recalls Cranberry Extract for Undeclared Soy Lecithin

    NOW Foods is recalling 3 bottles of cranberry extract capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.

    Product
    Cranberry extract packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighNHTSA·16V268000·2016-05-04

    Volvo Recalls 2016 XC90 Vehicles Due to Sunroof Switch Defect

    Volvo is recalling 2016 XC90 vehicles because the sunroof switch may be unintentionally pressed, causing the panel to close and increasing the risk of occupant injury.

    Product
    VOLVO — VOLVO XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1579-2016·2016-05-04

    Hologic Recalls CF InPlex ASR Cards Due to False Positive Results

    Hologic is recalling CF InPlex ASR Cards because they may produce false positive results or leak, potentially leading to unnecessary invasive testing during pregnancy.

    Product
    CF InPlex ASR Card; Catalog Number: 95-0501.
    Category
    Medical Device
    Distribution
    30 states
  • HighFDA (Food)·F-1129-2016·2016-05-04

    NOW Foods Andrographis Extract Recalled for Undeclared Soy Lecithin

    NOW Foods is recalling Andrographis extract 400 mg capsules due to undeclared soy lecithin. The product was distributed to 499 consignees in the US and one in Japan.

    Product
    Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-1578-2016·2016-05-04

    Roche IT3800 Hand-Held Barcode Scanner Recalled for Mis-Identification

    Roche Molecular Systems is recalling 6,939 IT3800 hand-held barcode scanners because they mis-identified sample barcodes when used with the COBAS AmpliPrep instrument.

    Product
    Hand-Held Scanner USB IT3800 For sample identification and tracking when used with various systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1585-2016·2016-05-04

    Shimadzu X-Ray Diagnostic Table Recalled for Unintentional Reverse Tilting

    Shimadzu Medical Systems is recalling 185 X-Ray Diagnostic Tables (Model YSF-300) due to reports of unintentional movement to reverse tilting.

    Product
    X-Ray Diagnostic Table, Model No. YSF-300 Use in combination with an X-ray high voltage generator, an X-ray tube unit, an Image intensifier and X-ray television unit, this table is applied for the following X-ray examinations: -X-ray T.V. fluoroscopy -Spot-filming -Bucky…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1568-2016·2016-05-04

    Intuitive Surgical Recalls da Vinci Xi Stapler Instruments Due to Motion Risk

    Intuitive Surgical is recalling 43 EndoWrist Stapler instruments for the da Vinci Xi system due to a risk of unexpected jaw motion during use.

    Product
    EndoWrist Stapler 45 and Stapler 30 instruments used on the da Vinci Xi systems (IS4000) with p5 software. General Surgery: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1132-2016·2016-05-04

    NOW Foods Recalls Goldenseal Root Supplements Due to Undeclared Soy Lecithin

    NOW Foods is recalling Goldenseal Root 500 mg capsules because they contain undeclared soy lecithin, a common allergen.

    Product
    Goldenseal Root 500 mg packaged in a white and orange bottle containing 100 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • ModerateFDA (Devices)·Z-1528-2016·2016-05-04

    Corin Trinity Acetabular Shell Recall Due to Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular Shells used in total hip replacements because the new packaging system may abrade the sterile barrier pouches.

    Product
    Trinity Acetabular Shell Product Usage Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1125-2016·2016-05-04

    Liquid Coffee Inc Recalls Concentrated Coffee Due to Elevated pH Levels

    Liquid Coffee Inc is recalling 642 gallons of concentrated coffee because the pH level was elevated above 4.6. The product was distributed nationwide to specific states.

    Product
    Concentrated coffee packed in 1/2 gallon or 1 gallon hermetically sealed Scholle or Liquibag.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1260-2016·2016-05-04

    Family Gourmet White Rice Recalled Due to Live Insects

    Family Dollar is recalling Family Gourmet Long Grain Enriched White Rice because live insects were found inside unopened bags.

    Product
    Family Gourmet Long Grain Enriched White Rice, 32 oz. (2 lb.) plastic bag (SKU: 1218898)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1567-2016·2016-05-04

    Boston Scientific Recalls Mislabeled Ultraflex Tracheobronchial Stents

    Boston Scientific is recalling four Ultraflex Tracheobronchial stents because 10mm diameter units were mislabeled as 12mm diameter.

    Product
    Boston Scientific Ultraflex Tracheobronchial Distal Release Stent System 12mm X 30mm Material Number: M00576550 The stent system is a permanently implanted expandable metal stent designed for palliation of tracheobronchial (TB) strictures. The system consists of a flexible…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1571-2016·2016-05-04

    Hardy Diagnostics Recalls GBS Detect Test Kits Due to Performance Failure

    Hardy Diagnostics is recalling GBS Detect test kits because product deterioration causes poor hemolytic reactions, potentially leading to inaccurate detection of Group B Streptococcus.

    Product
    Hardy Diagnostics GBS Detect Cat no. A300. Used for the isolation and detection by enhanced hemolysis of gamma-hemolytic (non-hemolytic) Group B Streptococcus.
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1575-2016·2016-05-04

    Mindray Panorama Patient Monitoring Network Recalled for Date Reversion

    Mindray DS USA is recalling Panorama Patient Monitoring Network units that may revert to the year 2000 during Daylight Savings Time.

    Product
    Panorama Patient Monitoring Network Mindray DS USA The Panorama Patient Monitoring can view recal time, store, print, graph and trend patient clinical and demographic data. The Panoram Patient Monitoring Network can sent independent alarm limits for data send by the bedside…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1564-2016·2016-05-04

    Hansen Medical Recalls Magellan Robotic Catheter Accessory Kits

    Hansen Medical is recalling eight Magellan Robotic Catheter Accessory Kits because one batch was radiated below the required dose.

    Product
    Magellan Robotic Catheter Accessory Kits, Model number MACC 50 and MACC80. Cardiology: The Hansen Medical Magellan System is a robotic control system that enables positioning and visualization of a Magellan Catheter and an off-the-shelf guide wire while allowing a physician…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1261-2016·2016-05-04

    Family Gourmet Brown Rice Recalled Due to Live Insects

    Family Dollar is recalling Family Gourmet Natural Whole Grain Brown Rice because live insects were found in unopened bags.

    Product
    Family Gourmet Natural Whole Grain Brown Rice, 32 oz. (2 lb.) plastic bag (SKU: 1230394)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2016·2016-05-04

    Synthes Periprosthetic Locking Screw Recalled for Post-Expiration Shipment

    Synthes (USA) Products LLC is recalling 15 units of 5.0 mm Periprosthetic Locking Screws shipped after their expiration date.

    Product
    5.0 mm Periprosthetic Locking Screw Self-tapping 12 mm Sterile; Catalog ID # 02.221.462S Indicated for fixation of various long bones.
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1527-2016·2016-05-04

    Corin Trinity Acetabular Shell Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular Shell devices used in total hip replacements due to a potential for abrasion of the sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular Shell Product Usage: Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1246-2016·2016-05-04

    Bissinger's Milk Chocolate Eggs Recalled for Mislabeling Artificial Vanillin as Vanilla

    Karl Bissinger, LLC is recalling Bissinger's Milk Chocolate Eggs because the product contains artificial vanillin but is labeled as containing vanilla.

    Product
    Bissinger's Milk Chocolate Eggs packaged in 6.5 oz (UPC 846107009382) Item: #11108 or 1 lb. (UPC 846107003458) Item: # 111049 plastic bags. Bissinger's Handcrafted Chocolatier, St. Louis, MO.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1526-2016·2016-05-04

    Corin Trinity Acetabular System Recalled for Packaging Abrasion Risk

    Corin USA Limited is recalling 629 Trinity Acetabular System devices due to potential abrasion of sterile barrier pouches in the new packaging system.

    Product
    Trinity Acetabular System Product Usage - Total Hip Replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1576-2016·2016-05-04

    Drew Scientific Recalls Drew3-PAC Reagent Packs Due to Platelet Background Issues

    Jas Diagnostics/Drew Scientific is recalling Drew3-PAC reagent packs because they may cause elevated platelet background during routine analyzer checks.

    Product
    Drew Scientific Inc. Drew3-PAC. This D3 Reagent Pack includes: diluent reagent 5L, enzymatic cleaner 750 mL, and a lysing reagent 125 mL.
    Category
    Medical Device
    Distribution
    20 states
  • ModerateFDA (Devices)·Z-1566-2016·2016-05-04

    Stryker PneumoSure Insufflators Recalled for Flow Rate Drop

    Stryker Endoscopy is recalling PneumoSure insufflators because the flow rate drops to zero when connected to a house gas source, suspending insufflation.

    Product
    PneumoSure XL High Flow Insufflator and PneumoSure High Flow Insufflator; High pressure units (HPU) (40L and 45L). Model Numbers: 620-040-610, 620-040-611, 620-040-613, 620-040-614, 620-040-600, 620-040-601, 620-040-602, 620-040-604, 105-210-684 The Pneumo Sure XL High…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1582-2016·2016-05-04

    Teleflex Pleur-evac Chest Drainage System Recalled for Missing Tyvek Bag Label

    Teleflex Medical is recalling Pleur-evac Chest Drainage Systems because the Tyvek bag label is missing, preventing identification of material code, lot number, and expiration date.

    Product
    Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product Usage: Pleur-Evacs are sterile, single-use, chest drainage systems intended for post-operative use
    Category
    Medical Device
    Distribution
    Distributed nationwide