The Recall Desk

State

Indiana product recalls

73,817 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.

These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45701–45725 of 83415

  • SevereNHTSA·17V724000·2017-11-17

    Forest River Recalls 2017-2018 Dynamax RVs for Carbon Monoxide Risk

    Forest River is recalling 2017-2018 Dynamax recreational vehicles because carbon monoxide may enter the cabin if the engine runs while parked.

    Product
    FOREST RIVER — FOREST RIVER DYNAMAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V727000·2017-11-17

    BMW Recalls 2018 X5 and X6 Models for Loose Suspension Bolts

    BMW is recalling 2018 X5, X5 M, X6, and X6 M vehicles because front suspension bolts may not be properly tightened, increasing crash risk.

    Product
    BMW — BMW X5, X5 M, X6 M, X6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V734000·2017-11-17

    Holiday Rambler Motorhomes Recalled for Defective Fire Extinguishers

    REV Recreation Group is recalling specific Holiday Rambler diesel motorhomes because the installed Kidde fire extinguishers may clog or detach, potentially failing to function during a fire.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER ENDEAVOR, NEPTUNE, AMBASSADOR, TRIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V723000·2017-11-17

    Newmar London Aire Motorhomes Recalled for Headlight Beam Defect

    Newmar is recalling 2015-2018 London Aire motorhomes because high beams fail to illuminate low beam bulbs, reducing visibility and increasing crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V730000·2017-11-17

    Freightliner Recalls 2018 Cascadia Trucks for Transmission Shift Bolt Defect

    Daimler Trucks North America is recalling 2018 Freightliner Cascadia trucks because a transmission shift lock bolt can seize, potentially causing the engine to stall and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·124-2017·2017-11-16

    Missa Bay LLC Recalls Chicken Wrap Kits Due to Undeclared Allergens

    Missa Bay LLC is recalling approximately 46 pounds of Fresh Prep'D Buffalo Style Ranch Wrap Kits because the products contain peanut and soy, which are not declared on the label.

    Product
    Missa Bay LLC — Missa Bay LLC Recalls Chicken Wrap Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·18037·2017-11-16

    Arctic Cat Recalls Wildcat ROVs Due to Winch Fire Hazard

    Arctic Cat is recalling 2017 Wildcat ROVs and winch kits because the winch solenoid can overheat and cause fires. No injuries have been reported.

    Product
    Arctic Cat ROVs with winches
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V722000·2017-11-16

    Spartan Recalls 2014-2017 Emergency Vehicles Due to Pressure Valve Defect

    Spartan Motors is recalling 2014-2017 Gladiator and MetroStar emergency vehicles because corroded rings may cause pressure relief valves to open, reducing water pressure for firefighting.

    Product
    SPARTAN — SPARTAN METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0083-2018·2017-11-15

    Teleflex Auto Endo5 Clip Applier Recalled for Clip Misalignment

    Teleflex Medical is recalling 13,710 units of the Auto Endo5 Automatic Hem-o-lok Clip Applier because clips may misalign, jam, or fall out of the device.

    Product
    WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0347-2018·2017-11-15

    21st Century Snack Foods Recalls Dark Chocolate Almonds for Undeclared Milk

    21st Century Snack Foods is recalling Dark Chocolate Almonds because the product contains undeclared milk, a major food allergen.

    Product
    21st CENTURY SNACK FOODS DARK CHOCOLATE ALMONDS Roasted Almonds Covered in Rich Dark Chocolate Net Wt. 6oz (170g) UPC: 0 30603 22854 9.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Devices)·Z-0075-2018·2017-11-15

    Terumo BCT Recalls Harvest Graft Delivery Packs Due to Seal Defect

    Terumo BCT is recalling 525 Harvest Graft Delivery Packs because some lots may lack a seal on the inner pouch, potentially compromising sterility.

    Product
    HARVEST TERUMOBCT, GCP-10 Graft Delivery Pack, REF 51449, Rx Only, STERILE EO Harvest Graph Delivery System is a disposable pack that takes the cell concentrate created while using the BMAC Procedure Packs and allows for hydration of bone graft material for application to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0076-2018·2017-11-15

    Sorin FlexFlow Venous Cannula Recalled for Sharpness Defect

    Sorin Group USA is recalling a specific lot of FlexFlow Venous Cannulas because they are sharper or pointier than expected.

    Product
    FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is a size 23 French with an outside diameter of 0.30 inch (7.7 mm) and an effective working length of 11.2 inch (28.5 cm). The FlexFlow Venous Cannula is an open…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0065-2018·2017-11-15

    Encore Medical Recalls Cobalt MV Bone Cement Due to Packaging Seal Loss

    Encore Medical is recalling 840 units of Cobalt MV Bone Cement because the sterile Tyvek packaging seal may be lost, potentially compromising sterility.

    Product
    Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0087-2018·2017-11-15

    Epimed RX-2 COUDE Epidural Needle Recalled for Potential Sterility Seal Defect

    Epimed International is recalling 500 units of RX-2 COUDE Epidural Needles due to a potential incomplete seal that may impact sterility.

    Product
    RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter
    Category
    Medical Device
    Distribution
    13 states