The Recall Desk

State

Indiana product recalls

73,366 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
2,528
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 2,528 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,587 recalls whose distribution notice names Indiana specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19451–19475 of 82953

  • ModerateFDA (Drugs)·D-0093-2023·2023-01-04

    Timolol Maleate Ophthalmic Solution recalled for failed stability specifications

    Apotex Corp. is recalling Timolol Maleate Ophthalmic Solution 0.5% (lot TA4844) nationwide due to failed stability specifications showing excessive weight loss that may affect medication potency.

    Product
    Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL, Rx Only, Mfg by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Mfg for: Apotex Corp. Weston, FL 33326, NDC 60505-1005-4
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0768-2023·2023-01-04

    Acumed Acutrak 2 Bone Screws Recalled for Distribution Without FDA Clearance

    Acumed is recalling Acutrak 2 bone screw products distributed without FDA pre-market clearance. Healthcare providers should contact Acumed or the FDA for guidance regarding use and management of these devices.

    Product
    Acutrak 2 Part Number/Part Description: 30-0021 25.0mm Acutrak 2¿ - 5.5 Screw 30-0021-S 25.0mm Acutrak 2¿ - 5.5 Screw 30-0023 30.0mm Acutrak 2¿ - 5.5 Screw 30-0023-S 30.0mm Acutrak 2¿ - 5.5 Screw 30-0025 35.0mm Acutrak 2¿ - 5.5 Screw 30-0025-S 35.0mm Acutrak 2¿ - 5.5…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0213-2023·2023-01-04

    XO Marshmallow Banana Puddin' OMG Recalled Due to Missing Product Label

    XO Marshmallow Limited Edition Banana Puddin' OMG is being recalled for missing product labels on packaging. The recall affects 526 retail units distributed in 27 U.S. states and internationally.

    Product
    XO Marshmallow Limited Edition: Banana Puddin' OMG (Ooey Marshmallow Goodness), 12oz. marshmallow fluff, 4 12oz. retail units per case
    Category
    Food
    Distribution
    27 states
  • ModerateFDA (Devices)·Z-0767-2023·2023-01-04

    Acutrak Bone Screws and Fusion Devices Recalled for Lack of FDA Pre-Market Clearance

    Acumed LLC is recalling Acutrak bone screws and fusion devices distributed without FDA pre-market clearance. Patients should contact their healthcare provider for guidance.

    Product
    Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw AM-0030-S 30.0mm Acutrak¿ 4/5 Bone Screw AM-0035-S 35.0mm Acutrak¿ 4/5 Bone Screw AM-0040-S 40.0mm Acutrak¿ 4/5 Bone Screw AM-0045-S…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·23083·2022-12-29

    ZLINE Gas Ranges Recalled for Carbon Monoxide Poisoning Risk

    ZLINE is recalling about 28,000 gas ranges because the oven can emit dangerous levels of carbon monoxide while in use, posing a serious risk of injury or death. The firm has received 44 reports of carbon monoxide emission, including three reports of consumers seeking medical attention.

    Product
    ZLINE 30-inch and 36-inch RG gas ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V957000·2022-12-29

    2022 Indian Chief Bobber Motorcycles Kickstand Failure Increasing Crash Risk

    Indian is recalling 2022 Chief and related motorcycles because the kickstand may not properly retract while riding. A failure to retract increases the risk of a crash.

    Product
    INDIAN — INDIAN CHIEF BOBBER DARK HORSE, SUPER CHIEF, CHIEF, CHIEF DARK HORSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23082·2022-12-29

    Inflatable Paddle Boards Recalled for Unexpected Deflation and Drowning Hazard

    Surf 9 is recalling Body Glove Tandem and ULI inflatable paddle boards sold at Costco because glue can separate at the seams, causing unexpected deflation and posing a drowning hazard. Three deflation reports have been received with no injuries yet reported.

    Product
    Body Glove Tandem Inflatable Stand Up Paddle Board, ULI Inventor Inflatable Paddle Board, ULI Zettian Inflatable Supyak and ULI Lila Inflatable Supyak
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V956000·2022-12-29

    2023 Volkswagen ID.4 Battery Cable Short-Circuit Fire Risk Recall

    Volkswagen is recalling certain 2023 ID.4 rear-wheel drive vehicles because the 12-volt battery charging cable may wear and cause a short circuit, risking vehicle fire and power loss. Dealers will inspect and repair or replace the cable at no charge.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23719·2022-12-29

    Yamaha Viking Off-Road Side-by-Side Vehicles Parking Brake Failure Recall

    Yamaha is recalling about 500 Viking Off-Road Side-by-Side vehicles because improper installation of parking brake retaining bolts could cause the brake to fail, allowing the parked vehicle to move unintentionally and potentially crash.

    Product
    Yamaha Viking Off-Road Side-by-Side vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0760-2023·2022-12-28

    Revaclear 400 Dialyzers Recalled for Potential Internal Blood Leaks

    Baxter Healthcare Corporation is recalling 3.6 million Revaclear 400 Dialyzers due to a manufacturing defect where a twisted gasket could cause internal blood leaks during hemodialysis treatment.

    Product
    Revaclear 400 Dialyzer. Product Code: 114746L. Used to treat chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0755-2023·2022-12-28

    GE Vivid S6 N Ultrasound Battery Fire Risk Recall

    GE Vivid S6 N ultrasound systems may experience battery failure, smoke, or fire if batteries are not replaced every 2 years as recommended. Clinicians should replace batteries per manufacturer Service Manual instructions.

    Product
    Vivid S6 N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0738-2023·2022-12-28

    Spinal implant insert may fail to disengage from vertebral body device

    NuVasive's X-CORE 2 spinal implants may not disengage properly from the vertebral replacement device, potentially requiring revision surgery. About 2,031 devices worldwide are affected.

    Product
    X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0751-2023·2022-12-28

    FDA Class II recall: Medical Action cardiac catheter introduction kit

    Medical Action Industries' Port a Cath Kit (cardiac catheter introduction kit) has been subject to an FDA Class II recall affecting 198 cases distributed in Virginia. The specific reason for recall was not provided by the FDA.

    Product
    Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0087-2023·2022-12-28

    Glycopyrrolate Tablets Recalled for Failed Impurities and Degradation Specifications

    Glycopyrrolate tablets distributed nationwide are being recalled due to failed impurities and degradation specifications. Patients with affected lots should discontinue use and consult their healthcare provider.

    Product
    GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2023·2022-12-28

    Revaclear 400 Dialyzers Recalled for Polyurethane Displacement Risk

    Baxter Healthcare is recalling Revaclear 400 dialyzers due to reports of polyurethane displacement, which could result in blood leaks during dialysis treatment. The recall affects over 6 million units distributed worldwide.

    Product
    Revaclear 400 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0726-2023·2022-12-28

    Corin BIOLOX DELTA Ceramic Hip Implant Heads Recalled for Incorrect Size Labeling

    Corin Ltd is recalling BIOLOX Delta Ceramic Hip Implant Heads nationwide due to size labeling errors. The 36XL size is labeled as 32XL and vice versa, which could result in implantation of an incorrectly sized component.

    Product
    Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0722-2023·2022-12-28

    GE Centricity Universal Viewer 6.0 Medical Imaging Software May Hide Studies

    GE Medical Systems' Centricity Universal Viewer 6.0 image display software may hide medical studies from users after IAS tool installation, requiring GE assistance to access hidden images and causing delays in reading diagnostic studies.

    Product
    Centricity Universal Viewer 6.0. Used to display medical images (Including mammograms) and data from various imaging sources.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0757-2023·2022-12-28

    GE Vivid q Ultrasound Systems: Battery Fire Risk Recall

    GE is recalling Vivid q ultrasound systems because batteries not replaced every 2 years as recommended may fail and emit smoke or catch fire.

    Product
    Vivid q ultrasound. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skeletal Conventional and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2023·2022-12-28

    Lamaze Chill Teether Recalled for Potential Microbial Growth in Fluid

    Lamaze Chill Teether teething rings are being recalled due to potential microbial growth in the internal fluid. This poses an infection risk, particularly for children with weakened immune systems.

    Product
    Lamaze Chill Teether, Fluid-Filled Teething Ring, Model No. Y5288L
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2023·2022-12-28

    Medical Action Industries Littauer Scissors Recalled for Debris Contamination

    Medical Action Industries is recalling Littauer surgical scissors because the sterile instruments may contain debris that could compromise their safety during clinical use.

    Product
    Medical Action Industries Inc. Disposable Instrument Pack, Littauer Scissor, REF 56247, packaged 1/package, 20 packages/box, 12 boxes/case, sterile.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0723-2023·2022-12-28

    ConvaTec AQUACEL Foam Ag Adhesive wound dressing recalled for visual contamination

    ConvaTec is voluntarily recalling AQUACEL Foam Ag Adhesive wound dressings due to visual contamination (brown spots) found on several dressings. Approximately 5,300 units distributed nationwide are affected.

    Product
    ConvaTec AQUACEL Foam Ag Adhesive, wound dressing advesive
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2023·2022-12-28

    Fresenius 2008T Hemodialysis Machines Recalled for False USB Device Alarm

    Fresenius Medical Care is recalling 2008T and 2008T Bluestar Hemodialysis Machines with CDX due to a software and hardware sensitivity to electromagnetic interference that triggers false alarms.

    Product
    2008T and 2008TBluestar Hemodialysis Machines with CDX-Indicated for acute and chronic dialysis therapy in a healthcare facility Models: (1) 190713 2008T HEMODIALYSIS SYS., with CDX; (2) 190766 2008T HEMODIALYSIS SYSTEM W/BIBAG W/CDX ; (3) 191124…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0759-2023·2022-12-28

    Ultrasound System Batteries May Fail, Emit Smoke, or Catch Fire

    GE Medical Systems is recalling Vivid q N ultrasound systems due to potential battery failures that could emit smoke or catch fire if batteries are not replaced per the 2-year service manual recommendation.

    Product
    Vivid q N ultrasound. Not marketed in the US. Used in ultrasound imaging and analysis in Fetal/Obstetrics; Abdominal/GYN; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular…
    Category
    Medical Device
    Distribution
    Distributed nationwide