The Recall Desk

State

Indiana product recalls

73,824 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,598
Critical
1,908
Severe
2,536
Most recent
2026-11-04

Of the 9,598 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49226–49250 of 83422

  • LowFDA (Drugs)·D-0671-2017·2017-04-19

    Jubilant Cadista Recalls Bupropion Hydrochloride Tablets for Impurity Failure

    Jubilant Cadista Pharmaceuticals is recalling Bupropion Hydrochloride Extended-release Tablets because high levels of a degradation product were detected.

    Product
    BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, packaged in a) 60-count bottles (NDC 59746-317-60) and b) 100-count bottles (NDC 59746-317-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1767-2017·2017-04-19

    Smiths Medical CADD Administration Set Recalled for Incorrect Filter Size Illustration

    Smiths Medical is recalling CADD Administration Sets because the illustration on the Instructions for Use incorrectly depicts the filter size as 2.0 microns instead of the actual 0.2 microns.

    Product
    CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
    Category
    Medical Device
    Distribution
    43 states
  • LowFDA (Drugs)·D-0669-2017·2017-04-19

    Jubilant Cadista Recalls Bupropion Hydrochloride Tablets for Impurity Issues

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-release Tablets due to high levels of a degradation product.

    Product
    BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 100 mg, packaged in a) 60-count bottles (NDC 59746-315-60) and b) 100-count bottles (NDC 59746-315-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E021000·2017-04-18

    Cummins Recalls ISV5.0 Diesel Engines in Tiffin Breeze Motorhomes

    Cummins is recalling ISV5.0 diesel engines in Tiffin Breeze motorhomes because a fan support bearing may fail, causing the engine to stall and increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V255000·2017-04-18

    Micro Bird Recalls MB II School Buses for Roof Crush Risk

    Micro Bird is recalling 2012-2017 MB II school buses because the roof may crush during a rollover, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V258000·2017-04-18

    Volvo Recalls 2015-2017 VHD Trucks for Incorrect Axle Weight Labels

    Volvo is recalling 2015-2017 VHD trucks because the Gross Axle Weight Rating on the certification label may be incorrect, which could lead to vehicle overloading.

    Product
    VOLVO — VOLVO VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V256000·2017-04-18

    Honda Recalls 2017 CR-V and Acura RDX for Fading Certification Labels

    Honda is recalling 2017 CR-V and Acura RDX vehicles because certification labels may wipe away with alcohol solvents, potentially leading to vehicle overload.

    Product
    ACURA — ACURA, HONDA RDX, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E020000·2017-04-13

    FiveCubits Recalls TREQ-VMx Tablets Due to Battery Overheating Risk

    FiveCubits is recalling TREQ-VMx mobile data tablets used by commercial truck operators because the lithium ion polymer batteries may overheat, increasing the risk of fire.

    Product
    ELECTRICAL SYSTEM:SOFTWARE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V253000·2017-04-13

    Nissan Recalls Sentra and Leaf Vehicles for Air Bag Defect

    Nissan is recalling 2014-2017 Sentra and 2015-2017 Leaf vehicles because the front passenger air bag may not deploy properly in a crash.

    Product
    NISSAN — NISSAN SENTRA, LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17132·2017-04-13

    Polaris Recalls Ranger 900 Vehicles Due to Fire and Burn Hazards

    Polaris is recalling about 51,000 Ranger 900 recreational off-highway vehicles because a heat shield can fall off, posing fire and burn hazards.

    Product
    Polaris Ranger 900 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17131·2017-04-13

    Bosch Recalls Roof-Mounted Solar Panels Due To Fire Hazard

    Bosch Solar Services is recalling about 28,000 roof-mounted solar panels because they can overheat and pose a fire risk. No injuries have been reported.

    Product
    Roof-mounted Bosch solar panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17740·2017-04-13

    Polaris Recalls Sportsman ATVs Due to Electronic Power Steering Malfunction

    Polaris is recalling about 3,800 model year 2017 Sportsman and Scrambler ATVs because the electronic power steering unit can malfunction, posing a crash hazard.

    Product
    Sportsman 450, 570, 850, 1000 and Scrambler 1000 all-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1848-2017·2017-04-12

    Biery Cheese Recalls Marketside Swiss Cheese for Listeria

    Biery Cheese, Inc. is recalling Marketside Grab and Go Swiss cheese because the supplier reported the product tested positive for Listeria monocytogenes.

    Product
    Marketside Grab and Go Swiss 10.8 oz Set Ups
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Food)·F-1853-2017·2017-04-12

    Vulto Creamery Recalls Handmade Miranda Cheese Due to Listeria Risk

    Vulto Creamery is recalling handmade Miranda cheese nationwide due to Listeria monocytogenes contamination. Consumers should discard or return the product.

    Product
    artisanal cheese VULTO Creamery HANDMADE CHEESE, Miranda, NET WT. 0.5 lbs,
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1831-2017·2017-04-12

    Lipari Foods Recalls Premo Sandwiches Due to Listeria Risk

    Lipari Foods is recalling Premo Signature Classic Italian sandwiches because a supplier recalled cheese contaminated with Listeria monocytogenes.

    Product
    Premo Signature Classic Italian, 1/6 oz.
    Category
    Food
    Distribution
    11 states
  • CriticalFDA (Drugs)·D-0637-2017·2017-04-12

    X-Gen Recalls Ibuprofen Lysine Injection Due to Particulate Matter

    X-Gen Pharmaceuticals is recalling 2,593 cartons of Ibuprofen Lysine Injection because of the presence of particulate matter. The affected product was distributed nationwide in the USA.

    Product
    IBUPROFEN LYSINE — IBUPROFEN LYSINE (IBUPROFEN LYSINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0644-2017·2017-04-12

    SCA Pharmaceuticals Recalls Vancomycin IV Bags Due to Particulate Matter

    SCA Pharmaceuticals is recalling Vancomycin HCl IV bags due to the presence of particulate matter, linked to a related Hospira recall.

    Product
    Vancomycin HCl 750 mg added to 250 mL 0.9% Sodium Chloride For IV Use Only, Rx Only, SCA Pharmaceuticals, Little Rock, AR 72205, NDC 70004-0929-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1857-2017·2017-04-12

    Vulto Creamery Recalls Blue Blais Cheese Due to Listeria Risk

    Vulto Creamery is recalling 13 wheels of Blue Blais artisanal cheese due to Listeria monocytogenes contamination. The product was sold nationwide, primarily in the Northeast, Mid-Atlantic, California, and Chicago.

    Product
    artisanal cheese VULTO Creamery HANDMADE CHEESE, Blue Blais
    Category
    Food
    Distribution
    Distributed nationwide