The Recall Desk

State

Indiana product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43701–43725 of 83415

  • ModerateFDA (Devices)·Z-1394-2018·2018-04-25

    GE Healthcare Lunar DPX Bone Density Systems Recalled for Data Errors

    GE Healthcare is recalling 43 Lunar DPX bone density systems because patient reports may be sent to hospital systems with incorrect names in the header.

    Product
    GE Healthcare Lunar: a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369 b) DPX MD+, Model Numbers: LU8230, LU40338, LU40352 Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared to a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1383-2018·2018-04-25

    Datascope Mega Intra-Aortic Balloon Catheter Recalled for Missing Contraindications

    Datascope is recalling 2,714 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions for Use are missing the Contraindications section.

    Product
    Intra-Aortic Balloon Catheter Mega 7.5FR 40cc Product Usage: The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0631-2018·2018-04-25

    Sandoz Recalls Triamterene and Hydrochlorothiazide Tablets Due to Cross-Contamination

    Sandoz Incorporated is recalling specific lots of Triamterene and Hydrochlorothiazide Tablets due to the presence of unrelated ingredients.

    Product
    Triamterene and Hydrochlorothiazide Tablets, USP, 75 mg/50 mg, 500-count bottles, Rx only, Manufactured by Sandoz, Inc., Princeton, NJ 08540, NDC 0781-5067-05.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1393-2018·2018-04-25

    GE Healthcare Lunar DPX Duo and Bravo Bone Density Software Recall

    GE Healthcare is recalling Lunar DPX Duo and Bravo bone density scanners because a software issue may cause reports to be filed under the wrong patient name in the hospital system.

    Product
    GE Healthcare Lunar: a) DPX Duo, Model Number: LU41693 b) DPX Bravo, Model Number: LU41692 Provides an estimate of BMD (Bone Marrow Density) at the lumbar spine and proximal femur regions. This BMD value can then be compared to a reference population at the sole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1418-2018·2018-04-25

    Terumo Sarns TCM II Recall for Updated Cleaning Instructions

    Terumo is recalling Sarns TCM II devices to update cleaning instructions. The recall covers 2,393 units distributed worldwide.

    Product
    Sarns TCM II, Catalog Numbers: 4415; 4416;164925; 164930;164935;164940 UDI 00886799000014 The Sarns TCM is indicated for controlling and monitoring patient temperature .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1384-2018·2018-04-25

    Datascope Mega Intra-Aortic Balloon Catheter Recalled for Missing Contraindications

    Datascope is recalling 655 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions For Use were missing the Contraindications section.

    Product
    Intra-Aortic Balloon Catheter Mega 7.5FR 30cc Product Usage: The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0629-2018·2018-04-25

    ACURE Clarifying Acne Towelettes Recalled for Poor Quality Water

    Diamond Wipes International is recalling ACURE clarifying acne towelettes because they were manufactured with poor quality water.

    Product
    ACURE, clarifying acne, glycolic + zinc (salicyclic acid 0.5%) towelettes, 30-count pouch, Distributed by Better Planet Brands, Fort Lauderdale, FL 33316, UPC 8 54049 00358 0.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1392-2018·2018-04-25

    Philips Ingenuity TF PET/CT Recalled for Unresponsive Acquisition Console

    Philips is recalling 12 Ingenuity TF PET/CT systems because the mass storage device may cause the acquisition console to become unresponsive, preventing image acquisition.

    Product
    Ingenuity TF PET/CT, Model No. 882442 Product Usage: The device is an integrated diagnostic X-ray Computed Tomography (CT) and Positron Emission Tomography (PET) system suitable for a wide range of diagnostic applications. The device utilizes the CT technology to obtain…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1417-2018·2018-04-25

    Terumo Sarns TCM Recall for Updated Cooler-Heater Cleaning Instructions

    Terumo is recalling Sarns TCM devices to update cleaning instructions for the cooler-heater component.

    Product
    Sarns TCM, Catalog No. 15747 The Sarns TCM is indicated for controlling and monitoring patient temperature .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1395-2018·2018-04-25

    GE Healthcare Prodigy Ultrasound Recall for Incorrect Patient Data in Reports

    GE Healthcare is recalling Prodigy and Prodigy Advanced ultrasound systems because bone density exam reports may be sent to PACS with incorrect patient information in the DICOM header.

    Product
    GE Healthcare: a) Prodigy, Model Numbers: LU7248, LU8905, LU40427, LU40431, LU40626, LU40637, LU40626, LU40637, LU42021, LU42025, LU41730, LU41734, LU42344, LU42365 b) Prodigy Advanced, Model Numbers: LU42361, LU42397 Provides an estimate of BMD (Bone Marrow Density) at…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1101-2018·2018-04-25

    Smucker Natural Foods Recalls Santa Cruz Organic Fruit Spread for Labeling Defects

    Smucker Natural Foods is recalling Santa Cruz organic blackberry pomegranate fruit spread because the labels are missing ingredient and firm information.

    Product
    SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10510 0
    Category
    Food
    Distribution
    28 states
  • LowFDA (Food)·F-1104-2018·2018-04-25

    Smucker Natural Foods Recalls Santa Cruz Organic Raspberry Spread for Labeling Defects

    Smucker Natural Foods is recalling Santa Cruz Organic Seedless Red Raspberry Fruit Spread because the product labels are missing the ingredient panel and firm information.

    Product
    SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10513 1
    Category
    Food
    Distribution
    28 states
  • LowFDA (Food)·F-1103-2018·2018-04-25

    Santa Cruz Organic Mango Fruit Spread Recalled for Missing Label Information

    Smucker Natural Foods is recalling Santa Cruz Organic Mango Fruit Spread because the product labels lack an ingredient panel and firm information.

    Product
    SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10516 2
    Category
    Food
    Distribution
    28 states
  • SevereNHTSA·18V260000·2018-04-24

    Hyundai Recalls 2017 Ioniq Hybrid Vehicles for Fire Risk

    Hyundai is recalling 2017 Ioniq Hybrid vehicles because a leaking oil seal may cause an electrical short, increasing the risk of a fire.

    Product
    HYUNDAI — HYUNDAI IONIQ HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18146·2018-04-24

    Honeywell Recalls Fibre-Metal E2 and North Peak A79 Hard Hats

    Honeywell is recalling specific Fibre-Metal E2 and North Peak A79 hard hats because they may fail to protect users from impact, posing a risk of head injury.

    Product
    Fibre-Metal E2 and North Peak A79 hard hats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V257000·2018-04-20

    Kia Recalls 2017 Niro Vehicles Due to Hybrid System Fire Risk

    Kia is recalling 2017 Niro vehicles because a leaking hydraulic clutch actuator seal may cause an electrical short, increasing the risk of a fire.

    Product
    KIA — KIA NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V255000·2018-04-20

    Altec Recalls 1992-2006 Digger Derrick Trucks Due to Boom Pivot Pin Failure

    Altec Industries is recalling 1992-2006 Digger Derrick trucks because a specific boom pivot pin may fail, causing unexpected boom movement that increases the risk of injury or death.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V256000·2018-04-20

    Supreme Recalls 2013-2017 Kold King Vehicles Due to Frame Rail Defect

    Supreme Corporation is recalling 2013-2017 Kold King vehicles because the floor frame rail may detach from cross members due to insufficient weld penetration.

    Product
    SUPREME — SUPREME KOLD KING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18145·2018-04-20

    Briggs & Stratton Recalls 3000 PSI Pressure Washer Surface Cleaners

    Briggs & Stratton is recalling 3000 PSI pressure washer surface cleaners because the spray bar can break and detach, posing an injury hazard.

    Product
    3000 PSI pressure washer surface cleaners
    Category
    Consumer Product
    Distribution
    Distributed nationwide