The Recall Desk

State

Indiana product recalls

73,598 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
1,908
Severe
2,534
Most recent
2026-10-24

Of the 9,592 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.

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30201–30225 of 83190

  • LowFDA (Devices)·Z-0126-2021·2020-10-28

    Invivo MR Coils Recalled for Incorrect IPX1 Water Ingress Rating Label

    Invivo Corporation is recalling 12,764 MR Coils because the labels were mistakenly printed with an IPX1 rating symbol, which indicates water ingress protection.

    Product
    MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0043-2021·2020-10-28

    ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date

    ANI Pharmaceuticals is recalling 408 bottles of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of 18 months.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0046-2021·2020-10-28

    ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date

    ANI Pharmaceuticals is recalling specific lots of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of the correct 18-month date.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0047-2021·2020-10-28

    ANI Pharmaceuticals Recalls Amphetamine Capsules Due to Incorrect Expiration Date

    ANI Pharmaceuticals is recalling specific lots of amphetamine extended-release capsules because they were labeled with a 24-month expiration date instead of the correct 18-month date.

    Product
    DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V657000·2020-10-27

    2021 Jeep Cherokee Front Lower Control Arm Fracture Recall

    Chrysler is recalling certain 2021 Jeep Cherokee vehicles because the front lower control arms may fracture while driving. This can cause loss of steering control and increase the risk of a crash.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V660000·2020-10-27

    Suspension snap-ring failure could cause wheel separation on Western Star 4700

    Daimler Trucks is recalling certain 2021 Western Star and Freightliner commercial trucks because the steer axle spindle nut snap-ring may be missing or improperly installed, potentially causing wheel separation and increased crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 4900, 5700, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V661000·2020-10-27

    Braun Recalls 2017-2020 Demers Ambulances for Seat Belt Defect

    Braun Ambulances is recalling 2017-2020 Demers TSE and EXE ambulances because the rear seat belt harness may separate from its mounting, increasing injury risk in a crash.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES, DEMERS EXE, TSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E082000·2020-10-27

    Leather on Wheels Recalls Polo Helmets for Impact Protection Defect

    Leather on Wheels is recalling Polo model helmets because they may not adequately reduce impact force, increasing the risk of injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V659000·2020-10-27

    Winnebago Era Recalled for Defective Front Seat Belt Anchor Weld Nut

    Winnebago is recalling 2012-2021 Era 170X vehicles because a weld nut was installed on the wrong side of the seat belt bracket, reducing retention strength.

    Product
    WINNEBAGO — WINNEBAGO ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V658000·2020-10-27

    Audi Recalls 2018-2020 Q7 Vehicles for C-Pillar Padding Defect

    Audi is recalling 2018-2020 Q7 vehicles because the C-pillar padding may not absorb enough impact in a crash, increasing injury risk for unbelted occupants.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V655000·2020-10-26

    2021 Forest River Cardinal Fifth-Wheel Trailers: Furnace Exhaust Intrusion Risk

    Forest River is recalling 2021 Cardinal fifth-wheel trailers. The furnace intake sleeve is too short and does not properly connect to the exterior, allowing furnace exhaust to enter the trailer and cause carbon monoxide poisoning.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V656000·2020-10-26

    2019-2021 Forest River Palomino Trailers Antenna Detachment Safety Recall

    Forest River is recalling 2019-2021 Palomino trailers because the antenna wing may not be properly secured, allowing it to detach while moving and create a road hazard.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V654000·2020-10-26

    Forest River Cherokee recreational trailers recalled for electrical fire risk

    Forest River is recalling 2019-2021 Cherokee recreational trailers due to inadequate wiring insulation on shore cord inlets, which can increase fire risk. Owners should contact Forest River for recall details.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V651000·2020-10-23

    Mercedes-Benz Recalls 2020 GLC Models for Steering Wiring Defect

    Mercedes-Benz is recalling 2,533 2020 GLC models because a damaged steering wiring harness could cause loss of power assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, AMG GLC63, AMG GLC43, GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V650000·2020-10-22

    GM Recalls 2019-2020 Silverado and Sierra Trucks for Driveshaft Defect

    General Motors is recalling 2019-2020 Chevrolet Silverado and GMC Sierra trucks because a driveshaft joint may not be properly welded, risking separation and loss of propulsion.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21704·2020-10-22

    Rocky Mountain Oils Recalls Wintergreen Essential Oil and Blends for Packaging Defect

    Rocky Mountain Oils is recalling Wintergreen essential oil and four oil blends because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Wintergreen essential oil, and Pain Ease, Sports Pro, True Blue, Relieve Me oil blends
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0016-2021·2020-10-21

    Seneca Cinnamon Apple Crisps Recalled for Salmonella Contamination

    Seneca Foods is recalling Cinnamon Apple Crisps due to potential Salmonella contamination. The recall covers specific brands and sizes distributed nationwide.

    Product
    Cinnamon Apple Crisps packaged under the following Brands and sizes: 1. Seneca, 2.5 ounce, UPC 0 18195-70100 8; 2. Clancy's 2.5 ounce, UPC 41498-27266. 3. Seneca, 0.7 ounce, UPC 0 18195-70140 4 4. Seneca 20 lb. 1" dices, product code 10134
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0083-2021·2020-10-21

    Country Fresh Cantaloupe Chunks Recalled for Listeria Contamination Risk

    Country Fresh Inc. is recalling specific lots of Cantaloupe Chunks due to potential Listeria monocytogenes contamination. Consumers should check their packages and discard or return the product.

    Product
    Cantaloupe Chunks 16oz UPC 681131180153; Cantaloupe Chunks 10oz UPC 681131180146 packaged in clear plastic containers
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0086-2021·2020-10-21

    Country Fresh Pineapple, Grapes, and Mango Blend Recalled for Listeria Risk

    Country Fresh Inc. is recalling 16oz Pineapple, Grapes, and Mango Blend due to potential Listeria monocytogenes contamination. The product was distributed in nine states.

    Product
    Pineapple, Grapes, and Mango Blend 16oz UPC 68113118039
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0091-2021·2020-10-21

    Country Fresh Summer Blend Recalled for Listeria Contamination Risk

    Country Fresh Inc. is recalling Summer Blend salad due to potential Listeria monocytogenes contamination. The product was distributed in nine states.

    Product
    Summer Blend 5oz UPC 681131355094 packaged in clear plastic container
    Category
    Food
    Distribution
    9 states
  • CriticalFDA (Food)·F-0080-2021·2020-10-21

    Country Fresh Mango Products Recalled for Listeria Contamination Risk

    Country Fresh Inc. is recalling specific mango products due to potential Listeria monocytogenes contamination. Consumers should check for the specific lot number and UPCs listed.

    Product
    Mango Spears 16 oz UPC 681131180382; Mango 10 oz UPC 681131180375; Mango Chunks 5.5 oz UPC 74641018410 all packaged in clear plastic containers
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-0084-2021·2020-10-21

    Country Fresh Pineapple Products Recalled for Listeria Risk

    Country Fresh Inc. is recalling specific pineapple products due to potential contamination with Listeria monocytogenes.

    Product
    Pineapple 32oz UPC 681131180443; Pineapple Chunks 10oz UPC 681131180429; Pineapple Chunks 16oz UPC 681131180467; Pineapple 42oz UPC 681131180436; Pineapple chunks 5.5 oz UPC 74641011862 all packaged in clear plastic containers
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-0096-2021·2020-10-21

    Handicare SwiftHook Component Recall for Mobile and Ceiling Lifts

    Handicare AB is recalling SwiftHook components used in mobile and ceiling lifts because the carry bar may detach during use, posing a risk of injury to patients and caregivers.

    Product
    SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0078-2021·2020-10-21

    Seasonal Fruit Tray 40oz May Be Contaminated With Listeria Monocytogenes

    The FDA is recalling Seasonal Fruit Trays 40oz due to potential Listeria monocytogenes contamination. Consumers should not consume these products until further notice.

    Product
    Seasonal Fruit Tray 40oz UPC 681131180238 packaged in a clear plastic container
    Category
    Food
    Distribution
    9 states