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.

126–150 of 83162

  • SevereFDA (Drugs)·D-0032-2027·2026-10-14

    FDA Recalls Tri-MIX Syringes Due to Sterility Assurance Concerns

    Carolina Infusion, LLC is recalling Tri-MIX compounded syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/40, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0072-2027·2026-10-14

    Steris VERIFY Biological Indicator Recall Due to Spore Population Concerns

    Steris is recalling VERIFY Dual Species Self-Contained Biological Indicators because spore populations may fall below specifications, potentially leading to false sterilization results.

    Product
    VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3060
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0004-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Leader Advanced Relief Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling Leader Advanced Relief Eye Drops and related brands due to a lack of assurance of sterility. The recall covers 208,896 cartons distributed nationwide.

    Product
    LEADER ADVANCED RELIEF EYE DROPS — LEADER ADVANCED RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0037-2027·2026-10-14

    Apothecary NAD+ Injection Recalled for Lack of Sterility Assurance

    Apothecary Pharma is recalling NAD+ Injection vials due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Apothecary NAD+ Injection 200 mg/mL, 6 mL Sterile Multi-Dose Vial, Rx Only, Apothecary Pharma, LLC, 1913 Evans Road, Cary, NC, 27513, NDC 85091-011-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0108-2027·2026-10-14

    Canon Medical Alphenix INFX-8000C/B5 Recalled for Tabletop Shift Risk

    Canon Medical System is recalling one Alphenix INFX-8000C/B5 unit in Idaho due to a risk of tabletop shifting that could cause patient misalignment.

    Product
    Alphenix INFX-8000C/B5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V673000·2026-10-14

    Toyota Recalls Land Cruiser Hybrid Vehicles for Fuel Leak Risk

    Toyota is recalling 2024-2027 Land Cruiser Hybrid vehicles because a fuel tube connection may disconnect and leak fuel, increasing fire risk.

    Product
    TOYOTA — 2027 TOYOTA LAND CRUISER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0011-2027·2026-10-14

    Better Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk

    The Better Bakehouse Snack Company is recalling Donutful Chocolate Dipped Vanilla Cake Donuts due to undeclared milk. The product was distributed nationwide.

    Product
    Donutful Chocolate Dipped Vanilla Cake Donuts - 7.05oz/10ct.Case Configuration 5 count carton, 6 cartons per case. UPC 850041392103. Paperboard carton containing 5 individually wrapped packages of two donuts each. UPC: 850041392103. The Better Bakehouse Snack Co. 3651 Lindell…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0020-2027·2026-10-14

    Sweet Sensi THC Gum Drops Recalled for Staphylococcus aureus

    Sweet Sensi is recalling Passion Guava Kush THC gum drops nationwide due to the detection of Staphylococcus aureus.

    Product
    Sweet Sensi Elevated Edibles Hybrid Gum Drops - Passion Guava Kush 140mg THC. Product is packaged in sealable & flexible gold, purple and black metallic plastic mylar pouch and is sold in two sizes: 1) Net wt. Approx. 2.1oz (60g) 10 count and 2) Net wt. 6.3oz (180g) 30 count.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0029-2027·2026-10-14

    FDA Recalls Tirzepatide/Cyanocobalamin Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tirzepatide/Cyanocobalamin 76/2 mg/mL injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    TIRZEPATIDE/CYANOCOBALAMIN 76/2 MG/ML INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0005-2027·2026-10-14

    K.C. Pharmaceuticals Recalls Target Eye Drops for Sterility Concerns

    K.C. Pharmaceuticals is recalling multiple brands of eye drops due to a lack of assurance of sterility. The recall covers 1,435,830 cartons distributed nationwide.

    Product
    TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE — TARGET EYE DROPS MAXIMUM REDNESS RELIEF EYE (GLYCERIN, NAPHAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0014-2027·2026-10-14

    GIAS Food Inc. Recalls Lemon Alfredo Fettuccine for Listeria Contamination

    GIAS Food Inc. is recalling 1,174 cases of Lemon Alfredo Fettuccine due to contamination with Listeria monocytogenes. The product was distributed to retail locations nationwide.

    Product
    Lemon Alfredo Fettuccine packed in a yellow plastic sealed bag with pink and black lettering; label reads in part as "bettergoods Lemon Alfredo Fettuccine, MADE IN ITALY, NET WT 22 OZ, BEST if Used By: SEP 21 2027 L6081A, UPC 194346442706, DISTRIBUTED BY: Walmart Inc.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0107-2027·2026-10-14

    Polymedco Sediplast Tubes Recalled for Potential Blood Exposure

    Polymedco is recalling Sediplast tubes because pressure buildup may eject the cap, releasing blood and creating a biological hazard for operators.

    Product
    SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2027·2026-10-14

    FDA Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to processing equipment.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS),30/1/10, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0085-2027·2026-10-14

    Stryker Bard EP XT Decapolar Steerable Diagnostic EP Catheter Recalled for Sterile Barrier Breach

    Stryker is recalling Bard EP XT Decapolar Steerable Diagnostic EP Catheters due to a potential sterile barrier breach that could lead to particulate embolization, infection, or thrombus formation.

    Product
    BARD EP XT DECAPOLAR STEERABLE, DIAGNOSTIC EP CATHETER, 6F, LARGE 4.0, 10, 2-5-2MM, REF: 201007
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0017-2027·2026-10-14

    biQ-FEL Beverage Recalled for Undeclared Sildenafil and Tadalafil

    A&P CREATIONS is recalling biQ-FEL beverage bottles containing undeclared Sildenafil and Tadalafil. The product was distributed nationwide.

    Product
    biQ-FEL, 16.9 fl oz (500 mL), 17 servings per bottle, Manufactured by ALMENAT SAS AV 39 OESTE No 10 OESTE-18 CALI VALLE INDUSTRIA COLOMBIANA; Distributed by: Biofel
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0031-2027·2026-10-14

    Carolina Infusion Recalls Tri-MIX Injectable Due to Sterility Concerns

    Carolina Infusion, LLC is recalling Tri-MIX injectable syringes due to a lack of assurance of sterility related to formulation and processing equipment.

    Product
    Tri-MIX (PAPAV/PHENTO/ALPROS),30/2/20, injectable, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0021-2027·2026-10-14

    FDA recalls injectable compounded mixture in single-use syringes

    Carolina Infusion LLC is recalling QUAD-MIX injectable compounded product nationwide due to sterility concerns.

    Product
    QUAD-MIX( PAPAV/PHENTO/ALPROS/TROP) INJECTABLE, Packaged in single-use dosage syringes, total mL dispensed based on dosage per specific patient prescription, Carolina Infusion LLC, 95 Bees Creek Road, Ridgeland, SC 29936
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2027·2026-10-14

    Philips Spectral CT Systems Recalled for Software Issues Affecting Safety

    Philips Medical Systems is recalling 539 Spectral CT systems due to software issues that may cause image artifacts, wrong slice thickness, or unintended system motion.

    Product
    Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model Numbers: 1. 728333 (U.S. and Outside U.S.), 2. 728340 (Outside U.S.), 3. 728344 (Outside U.S.), 4. 728345 (Outside U.S.);
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V674000·2026-10-14

    PACCAR Recalls 2027 Kenworth and Peterbilt Trucks for Bunk Restraint Defect

    PACCAR is recalling 310 model-year 2027 Kenworth and Peterbilt trucks because improperly secured sleeper bunk webbing may fail to restrain occupants during a crash.

    Product
    KENWORTH — KENWORTH, PETERBILT W900, W990, T880, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0073-2027·2026-10-14

    Steris VERIFY Dual Species Biological Indicator Recall for Spore Population Issues

    Steris Corporation is recalling VERIFY Dual Species Self-Contained Biological Indicators because the spore population may fall below specifications, potentially leading to false sterilization results.

    Product
    VERIFY Dual Species Self-Contained Biological Indicator Model/Catalog Number: S3061
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·N/A·2026-10-14

    Beak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination

    Beak & Skiff Sanitizer Alcohol Antiseptic 80% is being recalled because FDA analysis found acetaldehyde above specification limits in the product. The recall affects bottles distributed in New York and through online sales.

    Product
    Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding, 7447 Harwin Dr. Suite 111, Houston, TX 77036
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0101-2027·2026-10-14

    Avid Medical Recalls 30 DAVINCI LAP/GYN Kits for Lubricant Contamination

    Avid Medical, Inc. is recalling 30 DAVINCI LAP/GYN kits (Model WRNM037-16) because they may be contaminated with a lubricant used during manufacturing.

    Product
    DAVINCI LAP/GYN; Model/Item Number (Kit): WRNM037-16;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0090-2027·2026-10-14

    Onkos My3D Personalized Pelvic Implant Recalled for Distribution Error

    Onkos Surgical is recalling My3D Personalized Pelvic Implants that were inadvertently mixed up and distributed to incorrect customers.

    Product
    Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0095-2027·2026-10-14

    AVID Medical Recalls 33 Endovascular Packs Due to Lubricant Contamination

    AVID Medical, Inc. is recalling 33 Endovascular Packs (Model VAPX014-04) because they may be contaminated with a lubricant used during manufacturing.

    Product
    ENDOVASCULAR PACK; Model/Item Number (Kit): VAPX014-04;
    Category
    Medical Device
    Distribution
    Distributed nationwide