The Recall Desk

State

Indiana product recalls

73,722 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.

These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31351–31375 of 83318

  • HighNHTSA·20V440000·2020-07-28

    Honda Pilot Rearview Camera Software Defect Increases Crash Risk

    Honda is recalling certain 2019-2021 Pilot vehicles due to faulty software that may prevent the rearview camera from displaying properly. This increases the risk of crashes since drivers cannot see behind the vehicle.

    Product
    HONDA — HONDA ODYSSEY, PILOT, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V436000·2020-07-28

    Kia Recalls 2020 Telluride Vehicles for Trailer Brake Light Defect

    Kia is recalling 2020 Telluride vehicles equipped with Smart Cruise Control because trailer brake lights may not illuminate when the system applies brakes, increasing crash risk.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V426000·2020-07-27

    2019 Mercedes-Benz and Freightliner Sprinter Recall for Rear Leaf Spring Shims

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because incorrect rear leaf spring shims may affect handling and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V430000·2020-07-24

    Mercedes-Benz Recalls One 2020 GLE 350 for Seat Bolt Issue

    Mercedes-Benz is recalling one 2020 GLE 350 because a driver's seat bolt may not be installed correctly, which could increase injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V429000·2020-07-24

    Peterbilt 520 Recall: Steering Assist Bracket Bolts May Loosen

    PACCAR is recalling 2020 Peterbilt 520 trucks because incorrect bolts may allow the steering assist bracket to loosen, potentially locking the steering.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V431000·2020-07-24

    Great Dane Truck Body Recall for License Plate Light Misalignment

    Great Dane is recalling 2018-2020 Truck Bodies because the license plate light may aim rearward, failing federal safety standards and increasing crash risk.

    Product
    GREAT DANE — GREAT DANE TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V428000·2020-07-24

    RV generator transfer switch wiring defect may energize shore power connection

    Keystone Fuzion and Impact toy hauler travel trailers may have incorrectly wired generator transfer switches that could energize the shore power connection, creating an electrical shock hazard. Keystone will inspect and correct the wiring at no charge.

    Product
    KEYSTONE — KEYSTONE IMPACT, FUZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20765·2020-07-23

    Polaris Recalls Ranger, PRO XD, and Bobcat Utility Vehicles Due to Crash Hazard

    Polaris is recalling approximately 13,200 Ranger, PRO XD, and Bobcat utility vehicles because a defective clutch component can cause unexpected motion, posing a crash hazard.

    Product
    Model Year 2020 Ranger XP 1000 and Ranger CREW XP 1000 Off-Road Vehicles, Model Years 2019 - 2020 PRO XD 4000D UTVs, Model Year 2019 PRO XD 2000D UTVs, and Model Year 2020 Bobcat UV34 and UV34XL UTVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2553-2020·2020-07-22

    CME BodyGuard BodySet Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard BodySet infusion sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    BodyGuard BodySet, REF: A120-160SAS
    Category
    Medical Device
    Distribution
    49 states
  • CriticalFDA (Devices)·Z-2567-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Sets Due to Delivery Inaccuracy

    CME America, LLC is recalling BodyGuard Microset infusion sets because they may deliver therapy with significant inaccuracy, potentially causing over-infusion or under-infusion.

    Product
    BodyGuard Microset with Needleless Adaptor, REF: A120-003XSNY
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1109-2020·2020-07-22

    Fresh Express Recalls Hy-Vee Shredded Lettuce Due to Cyclospora Risk

    Fresh Express is recalling Hy-Vee Shredded Lettuce due to a possible health risk from Cyclospora. The product was distributed in 33 U.S. states and Canada.

    Product
    Hy-Vee Shredded Lettuce 8 oz., UPC 075450120530, Iceberg lettuce
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2574-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Sets Due to Delivery Inaccuracy

    CME America, LLC is recalling BodyGuard Microset infusion administration sets because they may deliver therapy with an inaccuracy exceeding plus/minus 13%, potentially causing over- or under-infusion.

    Product
    BodyGuard Microset, REF: A100-163XSL
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2569-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    CMExpress Microbore Set, REF: A120-161CYF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2596-2020·2020-07-22

    Skeletal Kinetics Recalls Acumed Impact Bone Void Filler Kits

    Skeletal Kinetics is recalling 41 units of Acumed Impact 5CC bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.

    Product
    ACUMED IMPACT 5CC. Product Number: 65-0105-S, UDI: 813845020252 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2585-2020·2020-07-22

    CME America Recalls Infusion Sets Due to Delivery Inaccuracy

    CME America is recalling Standard BodySet infusion sets because they may deliver therapy at inaccurate rates, potentially causing over- or under-infusion.

    Product
    Standard BodySet with Needleless Connectors, REF: A120-125XS
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1082-2020·2020-07-22

    Fresh Express Veggie Spring Mix Recalled for Cyclospora Risk

    Fresh Express is recalling Veggie Spring Mix 7 oz. bags due to a possible health risk from Cyclospora contamination.

    Product
    Fresh Express Veggie Spring Mix 7 oz., UPC 071279281049, Baby lettuce, carrots, red cabbage & radishes
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2580-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    CMExpress Microbore Sets, REF: A120-161C
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1056-2020·2020-07-22

    Fresh Express Chopped Kit Bacon & Bleu Recalled for Cyclospora Risk

    Fresh Express is recalling Chopped Kit Bacon & Bleu salads due to a possible health risk from Cyclospora. Consumers should not eat the product.

    Product
    Fresh Express Chopped Kit Bacon & Bleu 10.9 oz, UPC 071279306063, Red and green cabbage, green leaf lettuce, carrots & green onions
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1072-2020·2020-07-22

    Fresh Express Iceberg Garden Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Iceberg Garden salad products due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected lots.

    Product
    Fresh Express Iceberg Garden / Lechuga Repollo 3 lbs., UPC 071279104119, Iceberg lettuce, carrots & red cabbage
    Category
    Food
    Distribution
    32 states