The Recall Desk

State

Indiana product recalls

73,187 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
2,149
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 2,149 (22%) are Severe.

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14251–14275 of 82774

  • HighFDA (Devices)·Z-0606-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridges Recalled for Sodium Sensor Bias

    Siemens is recalling RAPIDPoint 500 Systems Measurement Cartridges because the sodium sensor can develop a negative measurement bias that could delay diagnosis of serious electrolyte disorders or cause treatment errors.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 100 -Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10844813
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0607-2024·2023-12-27

    RAPIDPoint 500 Diagnostic Cartridges Recall Due to Sodium Sensor Measurement Bias

    Siemens is recalling RAPIDPoint 500 measurement cartridges because the sodium sensor can produce inaccurate readings, potentially leading to delayed diagnosis or incorrect treatment of electrolyte imbalances.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491447
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0573-2024·2023-12-27

    Injection Needles Recalled for Inadequate Manual Cleaning Process

    Karl Storz is recalling 1,127 injection needles used in general and visceral surgery because the manual cleaning process cannot be adequately assured, potentially increasing infection risk for patients.

    Product
    Injection Needle, LUER-lock,0.8mm, REF: 26175PD
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0605-2024·2023-12-27

    Venous probe connection cable defects in Cardiohelp-i extracorporeal support systems

    Maquet Medical Systems USA is recalling venous probe connection cables for the Cardiohelp-i System due to insulation and wire breaks. Defective cables may prevent the system from receiving critical blood flow and temperature information.

    Product
    Venous probe connection cable (REF 701069333 and 701048804) used with the Cardiohelp-i System, part numbers 701072780 and 701041802
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2024·2023-12-27

    Vegan pumpkin pie products recalled due to foreign object contamination

    Willamette Valley Pie Company is recalling vegan pumpkin pie products distributed in 12 states due to foreign object contamination. The voluntary recall was initiated in November 2023.

    Product
    Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan Pumpkin Pie WFM, BAKED BULK, 6 units/case. KEEP FROZEN - TRANSPORT AND STORE AT LESS THAN ZERO DEGREES F. Just Thaw and serve. Remove from freezer, removed plastic…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-0574-2024·2023-12-27

    Injection needles recalled due to cleaning efficacy concerns

    Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery due to concerns that the manual cleaning process cannot ensure adequate sterilization, which may increase infection risk.

    Product
    Injection Needle, single cvd. 70 degrees, REF: 738750; Injection Needle, single cvd. 80 degrees, REF: 738752; Injection Needle, bayonet, 13 cm, REF: 738756; Injection Needle, angular, 13 cm, REF: 738758; Needle, bayonet-shaped, REF: 810505; Needle, Septum, angular, REF: 810506
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0577-2024·2023-12-27

    AcuMatch Hip System Recalled for Loss of Vacuum Integrity

    Exactech is recalling AcuMatch Hip System devices due to loss of vacuum in the inner-most vacuum bag, with 3 complaints reported affecting 4 devices. Vacuum loss could compromise device packaging integrity.

    Product
    AcuMatch Hip System, Catalog Number 142-32-27
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0572-2024·2023-12-27

    Injection needles and cannulas recalled for cleaning process efficacy issues

    Karl Storz Endoscopy is recalling injection needles and cannulas because the manual cleaning process may not effectively remove contaminants, potentially exposing patients to infection risk.

    Product
    Injection Needle, 3 Fr., REF: 27030N; Injection Cannula, 6 Fr., REF: 27182A
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0588-2024·2023-12-27

    Exactech Vantage Mobile Bearing Tibial Inserts Recalled Due to Vacuum Loss

    Exactech is recalling Vantage Mobile Bearing Tibial Inserts due to loss of vacuum in the innermost vacuum bag. Three complaints involving four devices have been reported.

    Product
    Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers: a) 350-41-23, b) 350-42-03
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0584-2024·2023-12-27

    Exactech Optetrak Logic PS Knee System Vacuum Loss Recall

    Exactech is recalling certain Optetrak Logic PS Knee Systems due to potential loss of vacuum in the inner-most vacuum bag. The company has received 3 complaints involving 4 devices.

    Product
    Exactech Optetrak Logic PS Knee System, Catalog Numbers: 02-012-35-5009
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0580-2024·2023-12-27

    Exactech Equinoxe Shoulder System recalled for loss of vacuum

    Exactech is recalling specific models of its Equinoxe Shoulder System implants due to loss of vacuum in the inner-most vacuum bag. Four devices have been affected according to three complaints received.

    Product
    Exactech Equinoxe Shoulder System, Catalog Numbers: a) 314-23-02, b) 314-23-03, c) 314-23-13, d) 314-23-14, e) 314-23-15, f) 314-24-22, g) 314-24-23, h) 314-24-24, i) 314-24-32, j) 314-24-33, k) 314-24-34, l) 314-24-35
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0571-2024·2023-12-27

    Injection Needle Recall Due to Cleaning Process Concerns

    Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery because the manual cleaning process cannot be assured effective, which may expose patients to a higher risk of infection.

    Product
    Injection Needle, REF: 25207
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0582-2024·2023-12-27

    Exactech Optetrak Knee Implant System Recalled for Vacuum Seal Failure

    Exactech is recalling specific catalog numbers of the Optetrak Knee Implant System due to loss of vacuum in the protective inner bag. Three complaints affecting four devices have been reported.

    Product
    Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d) 200-02-35, e) 200-02-38, f) 200-02-41, g) 200-03-32, h) 200-07-29, i) 200-07-32, j) 200-07-35, k) 204-21-13, l) 204-22-26, m) 208-23-18, n) 208-24-13
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0578-2024·2023-12-27

    Hip Implant Liner Recalled Due to Loss of Vacuum in Inner Bag

    Exactech has recalled certain Alteon Hip XLE Liner hip implant components due to vacuum loss in the inner vacuum bag. The company has received 3 complaints involving 4 devices related to this issue.

    Product
    Exactech Alteon Hip XLE Liner, Catalog Numbers: a) 01-030-40-0636, b) 01-030-40-0640, c) 01-030-42-0536
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0560-2024·2023-12-27

    Roche Cobas Interface Module Firmware May Cause Delayed Sample Processing

    Inpeco is recalling firmware versions for the Roche Cobas 8000 and PRO Interface Module that may cause delayed sample tube processing in laboratory automation systems.

    Product
    Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- IVD FlexLab Automation System -a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. Hardware versions…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0586-2024·2023-12-27

    Exactech knee replacement inserts recalled for vacuum seal loss

    Exactech is recalling Truliant and Activit-E knee replacement inserts for loss of vacuum in storage packaging. The defect was identified in 3 complaints involving 4 devices, with no reported injuries.

    Product
    Exactech Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032, c) 02-023-02-0035, d) 02-023-02-0038, e) 02-024-35-1512, f) 02-024-35-1515, g) 02-024-35-1519, h) 02-024-35-2010, i) 02-024-35-2013, j) 02-024-35-2015, k)…
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Devices)·Z-0595-2024·2023-12-27

    CARDIOHELP-i Heart-Lung Support System not properly tested for leakage current

    The CARDIOHELP-i Heart-Lung Support System was not properly tested to measure leakage current, an electrical safety concern. The FDA is recalling 1,594 units distributed worldwide.

    Product
    CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass (up to six hours). Product REF…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V900000·2023-12-26

    Volvo Recalls One 2020 VNL Truck for Steering Gear Assembly Defect

    Volvo Trucks North America is recalling one 2020 VNL truck because the steering gear assembly may have been assembled with fewer recirculating balls than required, potentially causing a loss of steering control.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V899000·2023-12-26

    2024 Mack Commercial Trucks Steering Gear Assembly Defect Recall

    Mack is recalling approximately 284 certain 2024 Pinnacle, Anthem, and Terrapro commercial trucks with incorrectly assembled steering gear assemblies that could cause loss of steering control and increase crash risk. Dealers will inspect and replace defective gears free of charge.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (PI/PN), TERRAPRO (TE)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V901000·2023-12-26

    2024 Hyundai Kona: Battery Cable Chafing May Cause Engine Fire

    Hyundai is recalling 2024 Kona vehicles because battery cables may chafe and short circuit, increasing the risk of engine compartment fire. Dealers will install protective sheathing at no cost.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V887000·2023-12-22

    Mack Trucks Recalls 2024 Granite Vehicles for Steering Knuckle Defect

    Mack Trucks is recalling 2024 Granite vehicles because bearing journals may not be fully seated in the steering knuckle assembly, which can lead to axle spindle fracture and increased crash risk.

    Product
    MACK — MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V905000·2023-12-22

    Ford vehicles recalled for oil pump belt failure and power braking loss

    Certain 2016-2018 Ford Focus and 2018-2022 Ford EcoSport vehicles may have faulty oil pump drive belts or tensioners that can fail, causing engine stall and loss of power braking assist, increasing crash risk.

    Product
    FORD — FORD ECOSPORT, FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V894000·2023-12-22

    Rosenbauer Fire Apparatus Recalled for Electrical Circuit Overload Risk

    Rosenbauer America is recalling specific fire apparatus models due to a firmware defect that can cause electrical circuits to overload and overheat, increasing the risk of fire.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL F-350, COMMERCIAL F-550, WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide