The Recall Desk

State

Indiana product recalls

73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30701–30725 of 83314

  • LowFDA (Devices)·Z-2976-2020·2020-09-23

    Oxford Immunotec Recalls T-SPOT.TB8 Kits Due to Incorrect Expiration Dates

    Oxford Immunotec is recalling 583 T-SPOT.TB8 test kits because they have incorrect expiration dates on the labeling.

    Product
    Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the diagnosis of Mycobacterium tuberculosis infection by detecting effector T cells that respond to stimulation by M. tuberculosis antigens ESAT-6 and CFP10, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V570000·2020-09-22

    Nissan Recalls 2020 Altima, Maxima, and Leaf for Rear Window Defect

    Nissan is recalling 2020 Altima, Maxima, and Leaf vehicles because the rear window glass may not remain properly secured, increasing crash risk.

    Product
    NISSAN — NISSAN LEAF, ALTIMA, MAXIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V571000·2020-09-22

    Pierce Fire Apparatus Recalled for Joystick Controller Defect

    Pierce Manufacturing is recalling 2018-2020 Arrow XT, Dash, Enforcer, Impel, Quantum, and Velocity vehicles because the joystick controller may cause the aerial device to move without operator input.

    Product
    PIERCE — PIERCE DASH, IMPEL, ARROW XT, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V568000·2020-09-21

    Nova Bus Recalls LFS Models Due to Power Steering Pipe Separation Risk

    Nova Bus is recalling 2019-2021 LFS and LFS ARTIC transit buses because power steering pipes may separate, causing fluid leaks and loss of steering assist.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V569000·2020-09-21

    2021 Genesis G70 vehicles recalled for fuel pump assembly defects

    Hyundai recalls 2021 Genesis G70 vehicles (2.0L GDI engines) for a fuel pump defect. A manufacturing burr may block fuel flow, potentially causing engine stalls and crash risk.

    Product
    GENESIS — GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V565000·2020-09-18

    Braxton Creek Bushwhacker Travel Trailer Recall for Floor Separation Risk

    Braxton Creek is recalling 2020-2021 Bushwhacker travel trailers because undersized lag bolts may allow the floor to separate from the frame, increasing crash risk.

    Product
    BRAXTON CREEK — BRAXTON CREEK BUSHWACKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V566000·2020-09-18

    Newmar Recalls 2018-2021 Motorhomes Due to Tire Valve Stem Defect

    Newmar is recalling 2018-2019 Ventana and 2021 Canyon Star motorhomes because a tire valve stem extension may damage the inner wheel, risking loss of tire pressure and a crash.

    Product
    NEWMAR — NEWMAR VENTANA, CANYON STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V563000·2020-09-18

    Travel trailer brake system defect increases crash risk during separation

    Forest River is recalling certain 2018-2021 travel trailers because the breakaway safety switch may not engage the trailer brakes during separation from the tow vehicle. This defect can cause loss of vehicle control and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, SONOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V562000·2020-09-17

    Motorhomes recalled for tire valve stem damage and pressure loss risk

    Forest River and Coachmen motorhomes (2018-2021) are recalled for tire valve stem damage that may cause pressure loss and crash risk. Owners should seek free replacement from the manufacturer.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, SPORTSCOACH, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E068000·2020-09-17

    Honda Recalls Tonneau Covers for 2017-2020 Ridgeline Trucks

    Honda is recalling specific tonneau covers for 2017-2020 Ridgelines because wind may cause panels to separate, creating a road hazard.

    Product
    HONDA — HONDA RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1428-2020·2020-09-16

    HelloFresh and EveryPlate Meal Kits Recalled Due to Salmonella Risk

    HelloFresh US is recalling approximately 694,090 meal kits containing onions received between June 25 and July 31, 2020, due to potential Salmonella contamination.

    Product
    Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
    Category
    Food
    Distribution
    46 states
  • SevereFDA (Drugs)·D-1564-2020·2020-09-16

    Just Hand Sanitizer Recalled for Methanol Labeling Error

    Open Book Extracts is recalling Just Hand Sanitizer because it was labeled to contain methanol.

    Product
    Just Hand Sanitizer (Ethyl Alcohol 73%) Single Use-Packs 100-count NDC 78065-2020-2 UPC 703123998598 (Single packs NDC 78065-2020-1 UPC 703123998659) Distributed by: Just Hand Sanitizer
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2909-2020·2020-09-16

    CareFusion Alaris System PC Unit Model 8015 Recalled for Keypad Defect

    CareFusion is recalling Alaris System PC Unit Model 8015 infusion pumps because fluid ingress can cause unresponsive or stuck keypad keys, potentially delaying or interrupting medication infusions.

    Product
    Alaris System PC Unit Model 8015
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Devices)·Z-2882-2020·2020-09-16

    CareFusion Recalls BD Alaris Modules for Incorrect Syringe Display

    CareFusion 303, Inc. is recalling BD Alaris Syringe and PCA Modules because they may display incorrect syringe types or sizes, potentially causing infusion errors.

    Product
    BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System; Syringe/PCA Sizer Sensor Replacement Kit, P/N 122278652
    Category
    Medical Device
    Distribution
    54 states
  • SevereFDA (Devices)·Z-2910-2020·2020-09-16

    CareFusion PC Unit Front Case with Keypad Replacement Kits Recalled

    CareFusion 303, Inc. is recalling PC Unit Front Case with Keypad Replacement Kits because fluid ingress may cause keys to become unresponsive or stuck, potentially delaying or interrupting life-sustaining infusions.

    Product
    PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY CASE FRONT W/KEYPAD 8015LS, TC10010217 ASSY FRT CASE W/ KEYPAD 8015 M2, TC10012515 ASSY FR CASE W/ KEYPAD 8015 M2, TC10013702 ASSY, CASE, FRONT W/KEYPAD, 8015LS, TC10013664 ASSY FR CASE W/ KEYPAD 8015 M2
    Category
    Medical Device
    Distribution
    52 states
  • SevereFDA (Food)·F-1424-2020·2020-09-16

    Signature Select Granola Bars Recalled for Undeclared Peanut Butter

    Treehouse Foods is recalling Signature Select Chewy Granola Bars because they may contain undeclared peanut butter. The recall covers 1,202 cases distributed nationwide and to Saudi Arabia.

    Product
    Signature Select Chewy Granola Bars, Chocolate Chip, Family Pack, 18 bars, UPC 021130-283637. 18-0.84 oz. Net Wt 15.2 oz (432g) Distributed By Better Living Brands LLC PO Box 99, Pleasanton, CA 94566-0009,
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1565-2020·2020-09-16

    Shine & Clean Hand Sanitizer Recalled for Methanol and Low Ethanol

    Maquiladora Miniara S.A. de C.V. is recalling Shine & Clean Hand Sanitizer gel because FDA testing found undeclared methanol and ethanol levels below the label claim.

    Product
    Shine & Clean Hand Sanitizer gel, (Ethyl Alcohol 70%), 33.81 fl oz (1L) bottle, Made in Mexico By: Maquiladora Miniara S.A. de C.V. Carrerera Teoloyucan Huehuetoca km: 22 S/N La Planada Mexico C.P.: 54665 NDC 76753-001-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1563-2020·2020-09-16

    Open Book Extracts Recalls Hand Sanitizer Labeled With Methanol

    Open Book Extracts is recalling Always Be Clean Hand Sanitizer because it is labeled to contain methanol. The recall covers 340,000 packs distributed nationwide.

    Product
    Always Be Clean Hand Sanitizer (73% Alcohol) 0.04 FL OZ (1.2 mL) packaged in a) Single snaps (NDC 75091-2020-1 UPC 375091202016); b) 100-count boxes (NDC 75091-2020-2 UPC 375091202023); c) 25-count boxes (NDC 75091-2020-3 UPC 375091202030)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2939-2020·2020-09-16

    CareFusion Recalls BD Alaris Infusion Pumps Due to Keypad Defects

    CareFusion is recalling BD Alaris infusion pumps because fluid ingress can cause unresponsive or stuck keys, potentially delaying or interrupting infusions.

    Product
    BD Alaris System PC Unit Model 8100 (Pump Module) and Pump Module Door Assembly Replacement Kits (P/N 49000239, 49000346, 49000438, 49000439) infusion pump.
    Category
    Medical Device
    Distribution
    54 states
  • HighFDA (Devices)·Z-2938-2020·2020-09-16

    Qiagen SARS-CoV-2 Test Panel Recalled for Influenza A False Positives

    Qiagen is recalling 1,474 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to an increased rate of false positive results for Influenza A, which may lead to inappropriate antiviral use or delayed diagnosis.

    Product
    QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative detection and differentiation of nucleic acid from multiple respiratory viral and bacterial organisms, including the SARS-CoV-2 virus, in nasopharyngeal swabs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20183·2020-09-16

    RH Recalls Industrial Three-Panel Mirrors Due to Injury Hazard

    RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.

    Product
    Industrial Three-Panel Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V560000·2020-09-16

    2020-2021 Kia Stinger fuel pump defect causing engine power loss

    Kia is recalling 2020-2021 Stinger vehicles because a fuel pump defect may block fuel flow to the engine, causing loss of power while driving and increasing crash risk.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide