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.

14076–14100 of 82774

  • ModerateFDA (Devices)·Z-0708-2024·2024-01-17

    Robotic Drill Recall: Users Unable to Resolve Disconnection Errors

    Blue Belt Technologies is recalling 1,859 CORI REAL INTELLIGENCE Robotic Drills (models ROB10013 and ROB10013S) because users cannot resolve drill disconnection error messages. No illnesses or injuries have been reported.

    Product
    CORI REAL INTELLIGENCE Robotic Drill, Product No. ROB10013 and ROB10013S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0687-2024·2024-01-17

    Bronchovideoscope Manual Cleaning Updated: Reusable Brushes No Longer Approved

    Olympus has updated cleaning instructions for the EVIS EXERA III Bronchovideoscope. Reusable brushes are no longer approved for manual cleaning; only single-use brushes should be used.

    Product
    Model No. BF-XP190, EVIS EXERA III Bronchovideoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0690-2024·2024-01-17

    Cysto-Nephro Videoscope Model CYF-VHR: Reusable Brush Cleaning Instructions Updated

    Olympus updated cleaning instructions for the Model CYF-VHR Cysto-Nephro Videoscope. Reusable brushes have been removed from manual cleaning procedures; single-use brushes remain compatible.

    Product
    Model No. CYF-VHR, CYSTO-NEPHRO VIDEOSCOPE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0685-2024·2024-01-17

    Cystonephrofiberscope Model CYF-5R Cleaning Procedure Recall: Reusable Brushes Removed

    Shirakawa Olympus Co., Ltd. is updating cleaning instructions for the Model CYF-5R Cystonephrofiberscope. Reusable cleaning brushes have been removed from manual cleaning procedures; single-use brushes remain approved.

    Product
    Model No. CYF-5R, Cystonephrofiberscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0658-2024·2024-01-17

    Medical Device Recall: Baxter Ostene Hemostasis Material Marketing Brochure Inaccuracy

    Baxter Healthcare is recalling marketing materials for the Ostene Hemostasis Material due to inaccuracies that do not align with the product's official Instructions for Use and Prescribing Information.

    Product
    Baxter Ostene Hemostasis Material, Product Codes: a) 1503831, 3.5 G; b) 1503832, 2.5 G; c) 1503833, 1.0 G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0692-2024·2024-01-17

    Videoscope Cleaning Instructions Updated: Reusable Brushes No Longer Compatible

    Shirakawa Olympus updated cleaning instructions for VISERA Cysto-Nephro Videoscopes, recommending removal of reusable brushes from manual cleaning procedures. Single-use brushes remain compatible.

    Product
    Model No. CYF-V2R, VISERA Cysto-Nephro Videoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0712-2024·2024-01-17

    QMS Tacrolimus Calibrators Recalled for Quality Degradation from Improper Storage

    Ortho-Clinical Diagnostics is recalling QMS Tacrolimus Calibrators Lot 74859619 due to improper storage that degrades product quality, potentially causing erroneous test results and testing delays.

    Product
    QMS Tacrolimus Calibrators, Product code 10015573
    Category
    Medical Device
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-0684-2024·2024-01-17

    Model CYF-5 cystonephrofiberscope cleaning instructions updated by Olympus

    Shirakawa Olympus has updated cleaning instructions for the Model CYF-5 cystonephrofiberscope, removing reusable cleaning brushes from the manual cleaning protocol while single-use brushes remain compatible.

    Product
    Model No. CYF-5, Cystonephrofiberscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0695-2024·2024-01-17

    SoClean 2 Supplemental Hose and Mask System Ozone Exposure Recall

    SoClean is recalling its SoClean 2 hose and mask maintenance system to reduce potential ozone gas exposure risks. An updated user manual and replacement adapter will be provided by the manufacturer.

    Product
    SoClean 2, REF SC1200, Supplemental Hose and Mask Maintenance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0657-2024·2024-01-17

    Baxter Coseal Premix Surgical Sealant: Marketing Brochure Information Inaccuracy

    Baxter Healthcare Corporation is recalling Coseal Premix Surgical Sealant due to inaccurate information in a marketing brochure that conflicts with the product's Instructions for Use and Prescribing Information.

    Product
    Baxter Coseal Premix, Surgical Sealant, Product Codes: a) 934070; b) 934071; c) 934072
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0666-2024·2024-01-17

    Cardiovascular Surgical Patch Marketing Brochure Contains Inaccurate Information

    Baxter is recalling marketing materials for Vascu-Guard Peripheral Vascular Patch because a brochure contains inaccurate information that conflicts with the product's official instructions and prescribing information.

    Product
    Vascu-Guard Peripheral Vascular Patch (US), Product Codes: a) VG0108: 0.8 X 8 CM US, TS; b) VG0110: 1 X 10 CM US, TS; c) VG0106: 1 X 6 CM US, TS; d) VG0209: 2 X 9 CM US, TS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0661-2024·2024-01-17

    Marketing brochure for Baxter Floseal hemostatic device contains inaccurate content

    Baxter Healthcare is recalling a cardiovascular surgery marketing brochure for Baxter Floseal Hemostatic Matrix Fast Prep because it contains inaccurate content that does not match the official product instructions and prescribing information.

    Product
    Baxter Floseal Hemostatic Matrix Fast Prep, Product Codes: a) ADS201844, 5 mL b) ADS201845, 10mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0705-2024·2024-01-17

    Shiloh Farms Bread for Life Organic 7 Grain Labeling Error Recall

    Shiloh Farms recalled 534 cases of Bread for Life Organic 7 Grain due to labeling error: cholesterol and sodium daily values listed in grams instead of milligrams. Product content is accurate.

    Product
    Shiloh Farms Bread for Life Organic 7 Grain UPC 0-47593-02812-7
    Category
    Food
    Distribution
    29 states
  • ModerateFDA (Devices)·Z-0664-2024·2024-01-17

    Peri-Guard Repair Patch marketing brochure contains inaccurate information

    Baxter Healthcare recalls a marketing brochure for Peri-Guard Repair Patch because it contains inaccurate information that does not match the product's Instructions for Use.

    Product
    Peri-Guard Repair Patch, Product Codes: a) PG1016 : 10 X 16 CMUS, TS b) PG1225: 12 X 25 CMUS, TS c) PG0404: 4 X 4 CMUS, TS d) PG0608: 6 X 8CMUS, TS e) PG0814: 8 X 14 CMUS, TS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0688-2024·2024-01-17

    FDA Recalls Rhino-Laryngofiberscope Cleaning Instructions for Brush Compatibility

    Shirakawa Olympus is recalling instructions for the Model ENF-XP Rhino-Laryngofiberscope. Reusable cleaning brushes have been removed from the manual cleaning procedure; single-use brushes remain compatible.

    Product
    Model No. ENF-XP, RHINO-LARYNGOFIBERSCOPE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0659-2024·2024-01-17

    Baxter Vascular Probe Marketed with Inaccurate Prescribing Information

    Baxter Healthcare is recalling its Vascular Probe due to inaccurate marketing materials that do not align with the product's official Instructions for Use. Providers should reference only the official IFU and PI.

    Product
    Baxter Vascular Probe, Product Codes: a) 7081015: 8CM, 1- 1.5 MM GLOBAL, b) 7081520: 8CM, 1.5-2 MM GLOBAL, c) 7082025: 8CM, 2-2.5 MM GLOBAL, d) 7151015: 15CM, 1-1.5 MM GLOBAL, e) 7151520: 15CM, 1.5- 2 MM GLOBAL, f) 7152025: 15CM, 2- 2.5 MM GLOBAL, g)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0667-2024·2024-01-17

    Baxter FloSeal Hemostatic Matrix brochure contains inaccurate clinical information

    A Baxter marketing brochure for FloSeal Hemostatic Matrix contains inaccurate content that does not match the product's official Instructions for Use and Prescribing Information.

    Product
    Baxter FloSeal Hemostatic Matrix NL, 5 mL, Product Codes: ADS201883
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0662-2024·2024-01-17

    Baxter FloSeal Hemostatic Matrix Recalled for Marketing Brochure Inaccuracies

    Baxter Healthcare Corporation is recalling Baxter FloSeal Hemostatic Matrix RECOTHROM products because the marketing brochure contains inaccurate information that does not align with the product's official Instructions for Use and Prescribing Information.

    Product
    Baxter FloSeal Hemostatic Matrix RECOTHROM, Product Codes: a) ADS202105, 5mL-6 PK US b) ADS202110, 10mL US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0686-2024·2024-01-17

    FDA updates cleaning instructions for EVIS EXERA III bronchovideoscope

    Shirakawa Olympus has updated cleaning instructions for the EVIS EXERA III bronchovideoscope. Reusable brushes are no longer approved for manual cleaning; single-use brushes remain compatible.

    Product
    Model No. BF-P190, EVIS EXERA III Bronchovideoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0665-2024·2024-01-17

    Peri-Guard Repair Patch Recall Due to Inaccurate Marketing Brochure

    Baxter Healthcare recalls Peri-Guard Repair Patch due to cardiovascular surgery marketing brochure containing inaccurate content that does not align with the product's Instructions for Use.

    Product
    Peri-Guard Repair Patch, Product Codes: a) PC1016NBIO: 10X16CMUS, b) PC1225NBIO: 12X25CMUS, c) PC0404NBIO: 4X4CMUS, d) PC0608NBIO: 6X8CMUS, e) PC0814NBIO: 8X14CMUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0707-2024·2024-01-17

    Bread Nutrition Label Unit Error: Shiloh Farms Organic Salt Free 7 Grain Bread

    Garden Spot Foods recalls Shiloh Farms Organic Salt Free 7 Grain Bread due to incorrect units on the nutrition label. Daily cholesterol and sodium values are listed in grams instead of milligrams, though the product content itself is accurate.

    Product
    Shiloh Farms Organic Salt Free 7 Grain Bread UPC 0-47593-02113-5
    Category
    Food
    Distribution
    29 states
  • HighNHTSA·24V017000·2024-01-15

    Peterbilt and Kenworth trucks recalled for detachable mirror glass

    PACCAR is recalling certain 2022-2024 Peterbilt and Kenworth trucks because the glass lock ring on the cab mirror assembly may not be fully seated, allowing the mirror glass to detach and reduce driver visibility.

    Product
    KENWORTH — KENWORTH, PETERBILT T180, 535, 537, 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V016000·2024-01-12

    E-One Recalls 280 Fire Apparatus Due to Steering Bracket Defect

    E-One is recalling 280 fire apparatus vehicles because an incorrectly machined steering assist bracket may reduce hydraulic force, increasing steering effort and crash risk.

    Product
    E-ONE — E-ONE CYCLONE E, CYCLONE N, TYPHOON N, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V014000·2024-01-11

    GM Recalls 2022 BrightDrop EV600 Vehicles Due to Fire Risk

    General Motors is recalling 2022 BrightDrop EV600 vehicles because the front-drive unit may leak oil, creating a risk of engine compartment fire.

    Product
    BRIGHTDROP — BRIGHTDROP EV600
    Category
    Vehicle
    Distribution
    Distributed nationwide