The Recall Desk

State

Indiana product recalls

73,363 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 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18326–18350 of 82950

  • HighNHTSA·23V191000·2023-03-23

    2020-2022 Jeep Wrangler Frame Stud Fuel Tank Puncture Recall

    Chrysler recalls 2020-2022 Jeep Wranglers because a frame stud may puncture the fuel tank during a crash, increasing fire risk. Approximately 35,829 vehicles are affected.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V194000·2023-03-23

    Helio O2 Travel Trailer Recall for Gas Leak Risk

    9299-5000 Quebec is recalling 2020-2023 Helio O2 travel trailers because internal burner tubes may fracture, causing a gas leak and increasing fire risk.

    Product
    HELIO — HELIO O2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23739·2023-03-23

    Arctic Cat Alterra 600 and Tracker 600 ATVs Recalled for Crash Hazard

    Textron Specialized Vehicles is recalling about 3,800 Arctic Cat Alterra 600 and Tracker 600 all-terrain vehicles because the A-arm can separate from the frame, causing loss of steering control and crash risk.

    Product
    Arctic Cat Alterra 600 and Tracker 600 All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V156000·2023-03-23

    Spartan Fire Recalls 2022-2024 Firetrucks Due to Transmission Software Defect

    Spartan Fire is recalling 2022-2024 Gladiator, Metro Star, FC-94, and KME Panther firetrucks because the transmission may fail to engage the water pump after reversing.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME FC-94, redundant PANTHER, GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V193000·2023-03-23

    Autocar Xpeditor Fuse Box Short Circuit from Water Intrusion

    Autocar is recalling 2020-2022 Xpeditor vehicles whose external fuse box may short circuit from water intrusion, causing unexpected stall and increasing crash risk. Dealers will mount the box vertically and install a protective shield.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23738·2023-03-23

    Burnham Commercial Natural Gas Boilers Recalled for Burn Hazard

    Burnham Commercial is recalling about 185 commercial natural gas boilers because delayed ignition and flame rollout can occur, posing a burn hazard. Two flame rollouts have been reported, but no injuries.

    Product
    Burnham Commercial Natural Gas Boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1190-2023·2023-03-22

    Closed Suction System Manifold Cracking Poses Respiratory Circuit Leak Risk

    Avanos Medical recalls BALLARD ACCESS Closed Suction System units due to manifold cracking, which can cause respiratory circuit leaks and inadequate ventilation in neonatal and pediatric patients.

    Product
    BALLARD* ACCESS Closed Suction System for Neonates/Pediatrics, Elbow Manifold.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V189000·2023-03-22

    Audi Recalls Q4 E-Tron SUVs Due to Air Bag Defect

    Audi is recalling 2022-2023 Q4 E-Tron vehicles because the head curtain air bag may tear during deployment, increasing injury risk.

    Product
    AUDI — AUDI Q4 E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0623-2023·2023-03-22

    Mead Johnson recalls ProSobee infant formula due to contamination risk

    Mead Johnson & Company is voluntarily recalling ProSobee Simply Plant-Based Infant Formula due to a remote possibility of cross-contamination with Cronobacter sakazakii. Affected batches were distributed across 40+ US states and territories, Puerto Rico, Thailand, and Guam.

    Product
    ENFAMIL PROSOBEE PWD 12.9OZ (6CAN) US
    Category
    Food
    Distribution
    39 states
  • SevereFDA (Devices)·Z-1189-2023·2023-03-22

    BALLARD ACCESS Closed Suction System Manifold May Crack and Leak

    Avanos Medical is recalling 780 units of the BALLARD ACCESS Closed Suction System due to manifold cracking that can leak the respiratory circuit, potentially causing inadequate ventilation in neonatal and pediatric patients.

    Product
    BALLARD ACCESS Closed Suction System for Neonates/Pediatrics, Y-Manifold.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0616-2023·2023-03-22

    Catalina Snacks Cheddar Snack Mix Recalled for Metal Contamination

    Catalina Snacks is recalling cheddar flavored snack mix due to metal foreign material contamination. Approximately 316,980 pouches with Best By dates of February 15 or 22, 2023 are affected.

    Product
    Cheddar flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468160) plastic stand up pouch.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Drugs)·D-0461-2023·2023-03-22

    Alprazolam Tablets Recalled for Potential Cross-Contamination from Manufacturing Deviations

    Breckenridge Pharmaceuticals is recalling Alprazolam 2 mg tablets nationwide due to manufacturing practice deviations creating potential cross-contamination risk. Affected tablets are distributed in 100-count and 500-count bottles.

    Product
    Alprazolam Tablets, USP, 2 mg, CIV, packaged in: a)100-count bottle (NDC 51991-0707-01) and b) 500-count bottle (NDC 51991-0707-05), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0614-2023·2023-03-22

    Catalina Snacks Honey Graham Cereal Recalled for Metal Contamination

    Catalina Snacks is recalling approximately 316,980 pouches of Honey Graham flavored cereal (UPC 860479001553) due to metal fragments. The affected product with a best-by date of 7/25/2023 was distributed online and across 21 states.

    Product
    Honey Graham flavored ready-to-eat cereal packaged in 9oz (UPC 860479001553) plastic stand up pouch.
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-1239-2023·2023-03-22

    BD Insulin Syringes Recalled for Sterility Defect

    Becton Dickinson recalls 1.9 million BD Insulin Syringes due to a nonsterility defect that could expose patients to pathogenic microorganisms and local infection risk.

    Product
    BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml, 12. 7mm, 28G Two Unit Scale- Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329424
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1246-2023·2023-03-22

    Synthes TFN-Advanced Femoral Nail Recalled for Dimensional Labeling Mismatch

    Synthes (USA) Products LLC is recalling TFN-Advanced Femoral Nails because labeled measurements do not match actual dimensions. Nails labeled 200mm may be 170mm and vice versa.

    Product
    TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 200MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.213S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1240-2023·2023-03-22

    BD Ultra-Fine Insulin Syringe 0.5mL Recalled for Nonsterility Risk

    Becton Dickinson is recalling approximately 1.1 million BD Ultra-Fine Insulin Syringes due to nonsterility concerns. The affected syringes may expose patients to pathogenic microorganisms and risk of local infection.

    Product
    BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326713
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0582-2023·2023-03-22

    Pingo Hot Chocolate Pods Recalled for Undeclared Peanut Residue

    Pingo hot chocolate pods may contain undeclared peanut residue. Consumers with peanut allergies should not consume affected products.

    Product
    Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1254-2023·2023-03-22

    Amicus MNC Apheresis Kit at Risk of Stress Leak in Centrifuge Packs

    Fenwal Inc is recalling certain batches of the Amicus MNC Apheresis Kit due to a potential for centrifuge packs to develop stress leaks. Affected units were distributed nationwide and internationally.

    Product
    Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator multiprocedural apheresis platform
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1244-2023·2023-03-22

    BD Ultra-Fine II insulin syringes recalled for sterility defect

    Becton Dickinson recalled 1,472,400 BD Ultra-Fine II insulin syringes due to a sterility defect. The nonsterile syringes pose a risk of local infection at injection sites.

    Product
    BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0459-2023·2023-03-22

    Alprazolam Tablets Recalled Due to Potential Cross-Contamination Risk

    Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.

    Product
    Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0581-2023·2023-03-22

    Coffee pods with undeclared peanut residue being recalled

    Two Rivers Coffee is recalling Brooklyn Bean Peanut Butter Cup Hot Cocoa pods because they may contain undeclared peanut residue. Consumers with peanut allergies should not use affected pods.

    Product
    Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single serve pods. Pods are packaged in the following Brooklyn Beans Variety Pack boxes: Brooklyn Beans Hot Chocolate Variety Pack Pods, 12 Count UPC:810683021977 Brooklyn Beans Brooklyn Beans Peanut Butter Chocolate Hot…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0460-2023·2023-03-22

    Alprazolam Tablets Recalled for Potential Cross-Contamination from Manufacturing Deviations

    Breckenridge Pharmaceutical is recalling Alprazolam 1 mg tablets distributed nationwide due to manufacturing practice deviations that pose a potential cross-contamination risk.

    Product
    Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0608-2023·2023-03-22

    Sunflower Lecithin Liquid Products Recalled for Undeclared Peanut Allergen

    Navada Imports is recalling sunflower lecithin liquid in bulk totes due to undeclared peanut allergen. The affected products were distributed nationwide to food manufacturers.

    Product
    Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.) totes
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0617-2023·2023-03-22

    Creamy Ranch Snack Mix Recalled for Metal Contamination

    Catalina Snacks recalls Creamy Ranch flavored snack mix due to metal contamination. Consumers who have this product should not eat it.

    Product
    Creamy Ranch flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468160) plastic stand up pouch.
    Category
    Food
    Distribution
    21 states