The Recall Desk

State

Indiana product recalls

73,570 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,592
Critical
1,913
Severe
2,529
Most recent
2026-10-24

Of the 9,592 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 2,529 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51–75 of 83162

  • ModerateFDA (Devices)·Z-0158-2027·2026-10-21

    Gore Viabil Short Wire Biliary Endoprosthesis Recalled for Incorrect Length Labeling

    W L Gore & Associates is recalling 32 units of GORE VIABIL Short Wire Biliary Endoprosthesis because they may be mislabeled with the incorrect length.

    Product
    Generic Name: GORE VIABIL Short Wire Biliary Endoprosthesis; Model/Catalog Number: VSWVH0808 and VSWVN1006 Product Description: The GORE VIABIL Short Wire Biliary Endoprosthesis is a flexible, self-expanding endoprosthesis designed to maintain luminal patency of the common…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0173-2027·2026-10-21

    Medline Recalls Surgical Convenience Kits with Non-Conforming Cannula Components

    Medline is recalling 620 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements, which may cause leaking or breaking during use.

    Product
    Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B; 2) EAR, Medline product number/SKU DYNJ909020A; 3) CAROTID PACK, Medline product number/SKU DYNJ42922C; 4) EAR, Medline product number/SKU DYNJ909020; 5) FEM CAROTID PACK…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0143-2027·2026-10-21

    Boston Scientific Recalls NaviFlex LW Pusher and Advx Panc. Stent

    Boston Scientific is recalling 403 units of NaviFlex LW Pusher and Advx Panc. Stent devices due to an incorrect manufacturing feature.

    Product
    NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0175-2027·2026-10-21

    Medline Recalls Surgical Convenience Kits with Non-Conforming Cannula Components

    Medline is recalling 235 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: 1) CV BASIN PACK-LF, Medline Product number/SKU DYNJ0538615K; 2) CV BASIN PACK-LF, Medline product number/SKU DYNJ0538615J; 3) CV BASIN PACK-LF, Medline product number/SKU DYNJ0538615L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0149-2027·2026-10-21

    BioFire FilmArray Pneumonia Panel Plus Recalled for Potential Contamination

    BioFire Diagnostics is recalling specific lots of FilmArray Pneumonia Panel Plus kits due to potential contamination that could cause false positive results.

    Product
    Generic Name: FilmArray¿ Pneumonia Panel plus Generic Name: FilmArray¿ Pneumonia Panel plus Model/Catalog Number: RFIT-ASY-0143 (30 Kit), RFIT-ASY-0142 (6 Kit) Software Version: N/A Product Description: Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0159-2027·2026-10-21

    Microgenics Recalls MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control

    Microgenics Corporation is recalling MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control products due to vial-to-vial variability that may delay patient PTH results.

    Product
    MAS Omni IMMUNE PRO Liquid Assayed Integrated Immunoassay Control, Level 1, REF: OPRO-101; MAS Omni IMMUNETM PRO Liquid Assayed Integrated Immunoassay Control, Sample Pack, REF: OPRO-SP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0148-2027·2026-10-21

    BioFire FilmArray Pneumonia Panel Recalled for Potential Contamination

    BioFire Diagnostics is recalling specific lots of FilmArray Pneumonia Panels due to potential contamination that could result in false positive test results.

    Product
    Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Catalog Number: RFIT-ASY-0144 (30 pack), RFIT-ASY-0145 (6 pack), FLM1-ASY-0150 (Verification Kits). Verification kit lots (FLM1-ASY-0150) are a sales configuration that consume kits from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0041-2027·2026-10-21

    Houston Rx LLC Recalls Sermorelin Vials Due to Process Control Issues

    Houston Rx LLC is recalling 7 vials of Sermorelin injectable solution due to a lack of process control. The product was distributed nationwide.

    Product
    Sermorelin, 1 mg/mL, 10 ml vial, Sterile injectable solution, RX Only, Houston RX LLC, 15430 Vantage Parkway E STE 220, Houston, TX 77032.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0189-2027·2026-10-21

    Medline Foot Ankle Convenience Kit Recalled for Shelf-Life Discrepancy

    Medline is recalling 30 Foot Ankle convenience kits due to a discrepancy in the shelf-life of a component.

    Product
    Medline convenience kit labeled as: FOOT ANKLE. Medline Kit SKU DYNJ65395A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0150-2027·2026-10-21

    BioFire Joint Infection Panel Recalled for Potential Contamination

    BioFire Diagnostics is recalling specific lots of the Joint Infection Panel due to potential contamination that could cause false positive test results.

    Product
    Generic Name: BioFire¿ Joint Infection (JI) Panel Generic Name: BioFire¿ Joint Infection (JI) Panel Model/Catalog Number: RFIT-ASY-0138 (30 Kit), RFIT-ASY-0135 (6 Kit) Software Version: N/A Product Description: Mulitple-type osteoarticular pathogen nucleic acid IVD, kit, nucleic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0142-2027·2026-10-21

    Neuronetics Recalls NeuroStar Advanced Therapy Systems Due to Non-Conforming Cables

    Neuronetics is recalling 179 NeuroStar Advanced Therapy Systems because the cables in the HP Coil Assembly do not meet product specifications.

    Product
    NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced Therapy Systems: 1. NeuroStar 2.0 US; Part Number: 81-01315-000. 2. NeuroStar 3.0 US; Part Number: 81-02315-000. 3. NeuroStar 2.X…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0188-2027·2026-10-21

    Healthmark Vinyl Instrument Guards Recalled for Labeling Non-Compliance

    Healthmark Industries is recalling 12.8 million vinyl instrument guards because their labeling does not comply with FDA regulations and steam sterilization instructions have been updated.

    Product
    Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUARD 1/16 X 3/4, Model Number 09-1-011; 3) VENTED INSTRUMENT GUARD 5/64 X 3/4 - BLUE, Model Number 09-1-012; 4) BLUE VENTED INSTRUMENT GUARD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0178-2027·2026-10-21

    Medline surgical convenience kits recalled for non-conforming cannula components

    Medline is recalling 165 surgical convenience kits because the cannula components do not meet ISO 80369-7 dimensional requirements and may leak or break during use.

    Product
    Medline surgical convenience kits labeled as: OPEN HEART, Medline Product Number/SKU DYNJ902898D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0185-2027·2026-10-21

    Medline Recalls CONMED AirSeal Access Port Kits Due to Overpressure Alerts

    Medline Industries is recalling 3,551 CONMED AirSeal Access Port kits due to potential overpressure alerts and system venting that may delay or end procedures.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0157-2027·2026-10-21

    In2bones Recalls Partially Threaded Bone Screws Due to Labeling Error

    In2bones USA, LLC is recalling 29 bone screws labeled as fully threaded but actually partially threaded due to a labeling error.

    Product
    REF: P65 ST862 CoLag SCREW, FT, 6.7X62.5 mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0184-2027·2026-10-21

    Medline recalls CONMED AirSeal Access Port kits due to pressure alerts

    Medline Industries is recalling 3,551 convenience kits containing CONMED AirSeal Access Ports because they may produce erroneous overpressure alerts and system venting.

    Product
    Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135A CHN GYN ONCOLOGY DYNJ906731M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0190-2027·2026-10-21

    Radiometer ABL90 FLEX Analyzers Recalled for Inaccurate Results

    Radiometer Medical ApS is recalling ABL90 FLEX and ABL90 FLEX PLUS analyzers due to a risk of potentially inaccurate results requiring updated instructions for use.

    Product
    The ABL90 FLEX and ABL90 FLEX PLUS analyzers are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting. These tests are only performed under a physician's order.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0187-2027·2026-10-21

    Merit Medical Systems Recalls Scout MD Delivery Systems Due to Deployment Issues

    Merit Medical Systems is recalling Scout MD Delivery Systems because the implantable clip may fail to deploy, preventing the reflector from functioning as intended.

    Product
    Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance System, Rx Only, Sterile-EO
    Category
    Medical Device
    Distribution
    7 states
  • LowFDA (Devices)·Z-0162-2027·2026-10-21

    Magellan LeadCare II Blood Lead Test Kit Recall for Labeling Error

    Magellan Diagnostics is recalling 321 LeadCare II Blood Lead Test Kits due to a potential expiration date labeling error that may delay test results.

    Product
    LeadCare II Blood Lead Test Kit. Model/Catalog Number: 70-6762.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V687000·2026-10-20

    Lexus NX Vehicles Recalled for Instrument Panel Display Failure

    Toyota is recalling 2022-2024 Lexus NX vehicles because the instrument panel may fail to display critical warnings, increasing crash risk.

    Product
    LEXUS — 2023 LEXUS NX PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V688000·2026-10-20

    Ford Recalls Lincoln Hybrid Vehicles for Transmission Defect

    Ford is recalling 2026-2027 Lincoln Nautilus and 2027 Corsair Hybrids because corrosion may cause the vehicle to unexpectedly shift into neutral while driving.

    Product
    LINCOLN — LINCOLN CORSAIR HYBRID, NAUTILUS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E073000·2026-10-20

    Ford Recalls ABS Modules With Incorrect Software Programming

    Ford is recalling certain Anti-Lock Brake System (ABS) modules that may have incorrect software, potentially degrading brake balance and increasing stopping distance.

    Product
    SERVICE BRAKES, HYDRAULIC:ANTILOCK/TRACTION CONTROL/ELECTRONIC LIMITED SLIP:CONTROL UNIT/MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V693000·2026-10-20

    Hyundai Recalls 2026 Models for Wheel Lug Nut Loosening Risk

    Hyundai is recalling 2026 Venue, Elantra N, Elantra Hybrid, and Elantra vehicles because wheel lug nuts may loosen, allowing the wheel to detach.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA HYBRID, VENUE, ELANTRA N
    Category
    Vehicle
    Distribution
    Distributed nationwide