The Recall Desk

State

Indiana product recalls

73,741 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,596
Critical
1,908
Severe
2,534
Most recent
2026-10-28

Of the 9,596 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 2,534 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37901–37925 of 83337

  • ModerateFDA (Devices)·Z-1341-2019·2019-05-22

    Siemens Artis Q Angiography Systems Recalled for Tabletop Movement Blockage

    Siemens Medical Solutions is recalling 459 Artis Q angiography systems because the floating tabletop movement may be blocked after a collision sensor activates.

    Product
    Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2019·2019-05-22

    Arrow PICC Recall for Incorrect Length Labeling

    Arrow International is recalling 963 Arrow PICC kits because some are labeled with the wrong length, potentially leading to incorrect clinical use.

    Product
    Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2 Product Usage: The Arrow Pressure Injectable PICC is indicated for short-term or longterm peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1364-2019·2019-05-22

    Barlean's Olive Leaf Complex Recalled for Undeclared Sulfites

    Barlean's is recalling Olive Leaf Complex softgels due to undeclared sulfites. Sulfite levels do not exceed 10 ppm.

    Product
    Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle. UPC 7 05875 70009 2. Item FG 10107, Barlean s, Olive Leaf Complex, 60 Softgels per bottle. UPC 7 05875 0008 5.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·056-2019·2019-05-21

    BEF Foods Recalls Bob Evans Beef Stroganoff Pasta Produced Without Inspection

    BEF Foods is recalling approximately 527 pounds of Bob Evans Beef Stroganoff Pasta produced without federal inspection. No adverse reactions have been reported.

    Product
    BEF Foods, Inc. — BEF Foods, Inc. Recalls Beef Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    7 states
  • SevereCPSC·19124·2019-05-21

    ION Audio Recalls Portable Speakers Due to Explosion Hazard

    ION Audio is recalling four models of portable speakers because hydrogen gas can leak from the battery, causing the speaker to burst and explode.

    Product
    Portable speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V383000·2019-05-21

    Honda Recalls 2019 CR-V Vehicles for Steering Wheel Air Bag Defect

    Honda is recalling 2019 CR-V vehicles because burrs on the steering wheel core may damage air bag wiring, potentially disabling the driver's air bag or causing it to deploy unexpectedly.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V381000·2019-05-20

    Newmar Recalls 2019-2020 Motorhomes Due to Brake Valve Defect

    Newmar is recalling 40 specific 2019 and 2020 motorhomes because a brake relay valve defect may cause extended stopping distances, increasing crash risk.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, LONDON AIRE, ESSEX, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V382000·2019-05-20

    Ducati Recalls Panigale Motorcycles Due to Fuel Tank Pressure Issue

    Ducati is recalling 2018-2019 Panigale motorcycles because excessive fuel tank pressure may cause fuel to spray when opening the cap, increasing injury and fire risks.

    Product
    DUCATI — DUCATI PANIGALE SPECIALE, PANIGALE V4 S, PANIGALE V4, PANIGALE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V380000·2019-05-19

    Heil AJB9-1040 Hybrid Trailers Recalled for Frame Cracking

    Entrans is recalling 2017-2020 Heil AJB9-1040 Hybrid trailers because frame cracks may develop, affecting handling and increasing crash risk.

    Product
    HEIL — HEIL AJB9-1040 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·055-2019·2019-05-18

    Vienna Beef Recalls Frankfurters Due to Possible Metal Contamination

    Vienna Beef Ltd. is recalling approximately 2,030 pounds of beef frank links that may contain metal. The products were shipped to food service locations in Illinois, Indiana, and Wisconsin.

    Product
    Vienna Beef Ltd. — Vienna Beef Ltd. Recalls Beef Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·054-2019·2019-05-17

    Caito Foods Recalls Chicken Salads Due to Undeclared Soy Allergen

    Caito Foods LLC is recalling approximately 1,767 pounds of ready-to-eat chicken salads because they contain undeclared soy, a known allergen.

    Product
    Caito Foods, LLC — Caito Foods LLC. Recalls Salads with Chicken Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·19V379000·2019-05-17

    Newell Recalls 2017-2020 P50 Motorcoaches Due to Wiper Linkage Defect

    Newell Coach Corp. is recalling 2017-2020 P50 motorcoaches because a short wiper arm linkage may cause the wiper to rotate downward, reducing visibility and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V376000·2019-05-16

    Micro Bird Recalls 2018-2019 School Buses for Solenoid Overheating Risk

    Micro Bird is recalling 2018-2019 G5 and T-Series school buses because a heavy-duty solenoid may overheat nearby components, potentially causing vehicle stoppage or fire.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 TRANSIT BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V378000·2019-05-16

    Honda and Acura Recall Vehicles Due to Passenger Air Bag Defect

    Honda is recalling 19,138 vehicles because the front passenger air bag inflator may be installed incorrectly, potentially preventing proper deployment in a crash.

    Product
    HONDA — HONDA, ACURA INSIGHT, CIVIC, ACCORD CROSSTOUR, CIVIC GX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1277-2019·2019-05-15

    Alvogen Recalls Fentanyl Transdermal Systems Due to Product Mix-Up

    Alvogen is recalling Fentanyl Transdermal Systems because a customer reported a carton labeled 12 mcg/h contained 50 mcg/h patches.

    Product
    FENTANYL SYSTEM — FENTANYL SYSTEM (FENTANYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1331-2019·2019-05-15

    Laduree Frozen Poppy Seed Bread Recalled for Elevated Morphine and Codeine

    Laduree USA is recalling frozen poppy seed bread containing elevated levels of morphine and codeine. The product was distributed to warehouses and restaurants in Washington DC and New York.

    Product
    Frozen Poppy Seed Bread (57 grams), UPC Codes: (01)03556420003673(15)191122(10)181122(91)0937326, Lot 22112018
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1272-2019·2019-05-15

    Zydus Recalls Acyclovir Tablets Due to Labeling Error with Carvedilol

    Zydus Pharmaceuticals is recalling Acyclovir 400 mg tablets because one bottle was found to contain Carvedilol 6.25 mg tablets due to a label mix-up.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V374000·2019-05-15

    Navistar Recalls 2017 IC CE Transit Buses for Brake Drag

    Navistar is recalling 2017 IC CE transit buses because the driver-side rear brakes may drag, posing a fire and injury risk.

    Product
    IC BUS — IC BUS CESB, CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1346-2019·2019-05-15

    El Guapo Chile Pods Recalled for Unlabeled Peanut Allergen

    Mojave Foods is recalling El Guapo Chile Pods due to an unlabeled peanut allergen. Consumers should check their pantry for the affected sizes and UPC codes.

    Product
    El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz
    Category
    Food
    Distribution
    28 states
  • SevereFDA (Devices)·Z-1296-2019·2019-05-15

    Abbott ARCHITECT cSystems ICT Module Recall for False Chloride Results

    Abbott is recalling ARCHITECT cSystems ICT Modules due to a potential for falsely elevated serum or plasma chloride results.

    Product
    Abbott ARCHITECT cSystems ICT Module, REF 09D28-03. Product Usage: The ARCHITECT cSystems ICT (Integrated Chip Technology) is used for the quantitation of sodium, potassium, and chloride in human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V373000·2019-05-15

    Navistar Recalls IC Bus School Buses Due to Rear Brake Drag

    Navistar is recalling 2016-2020 IC Bus school buses because the driver-side rear brakes may drag, potentially causing fire or injury.

    Product
    IC BUS — IC BUS RECB, CE, CESB, RESB
    Category
    Vehicle
    Distribution
    Distributed nationwide