The Recall Desk

State

Indiana product recalls

73,495 recalls have nationwide distribution and so reach Indiana. 9,589 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total
9,589
Critical
1,913
Severe
2,528
Most recent
2026-10-14

Of the 9,589 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,528 (26%) are Severe.

These figures cover only the 9,589 recalls whose distribution notice names Indiana specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24901–24925 of 83084

  • HighFDA (Food)·F-0305-2022·2021-12-29

    Vanilla Cupcakes Recalled Due to Potential Metal Contamination

    GIVE AND GO is recalling Favorite Day and Kimberley's bakeshoppe vanilla-filled cupcakes due to potential metal contamination. Affected products were distributed nationwide.

    Product
    Favorite Day Gourmet Vanilla filled cupcakes 11.7 oz. UPC 0 85239 42018 8 Kimberley's bakeshoppe Vanilla bean filled gourmet cupcakes 11.7 oz. UPC 7 70981 31117 3 Kimberley's bakeshoppe vanilla filled gourmet cupcakes 11.7 oz. UPC 7 70981 31003 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0313-2022·2021-12-29

    Wondershop Frosted Sugar Cookies Recalled for Potential Metal Contamination

    GIVE AND GO is recalling approximately 1,142,754 units of Wondershop at Target Frosted Sugar Cookies due to potential metal contamination in the product.

    Product
    Wondershop at Target Frosted Sugar Cookies 13.5 oz. UPC 0 85239 13621 8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0415-2022·2021-12-29

    Surgical Suction Instruments Recalled for Calibration Defect Risk

    Acclarent's TruDi NAV Suction Instruments may be incorrectly calibrated, affecting surgical navigation accuracy. If undetected, the error could cause tissue damage, arterial injury, or nerve damage.

    Product
    TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z
    Category
    Medical Device
    Distribution
    39 states
  • HighNHTSA·21V00N000·2021-12-29

    Kenworth and Peterbilt Commercial Trucks Recalled for Methane Detection System Failure

    PACCAR is recalling approximately 1,107 Kenworth and Peterbilt commercial trucks (2016–2022) due to methane detection system power loss. If the system loses electrical power, operators may not detect dangerous methane levels, increasing fire and injury risk.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, T880, 567, 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0414-2022·2021-12-29

    Skinny Needle with Chiba Tip recalled for debris contamination

    Cook Inc. is recalling Skinny Needles with Chiba Tip due to black debris on internal components that may cause local inflammatory reactions if the product is used.

    Product
    Skinny Needle with Chiba Tip. RPN 090010, 090010-ET; GPN G14254, G15290. Rigid needle available with EchoTip to provide enhanced visualization of needle tip when used with ultrasonic imaging equipment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0310-2022·2021-12-29

    Freshness Guaranteed Cookies N' Creme Tiny Pies Recalled for Metal Contamination

    Freshness Guaranteed Cookies N' Creme Tiny Pies (12.7 oz., UPC 0 78742 37636 3) are being recalled nationwide due to potential metal contamination in the product.

    Product
    Freshness Guaranteed Cookies N' Creme Tiny Pies 12.7 oz. UPC 0 78742 37636 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0304-2022·2021-12-29

    Give and Go Kids Cupcakes Recalled for Potential Metal Contamination

    Give and Go Prepared Foods Corp. is recalling Kids Cupcakes chocolate and vanilla in 21.9 oz. packages nationwide due to potential metal contamination in the product.

    Product
    Give and Go Prepared Foods Corp. Kids Cupcakes chocolate & vanilla kids cupcakes 21.9 oz. UPC 7 70981 31091 6
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0306-2022·2021-12-29

    Triple Chocolate Gourmet Cupcakes Recalled for Potential Metal Contamination

    Kimberley's bakeshoppe and Favorite Day brand triple chocolate filled gourmet cupcakes are being recalled nationwide due to potential metal in the product. Consumers should not eat the affected products.

    Product
    Kimberley's bakeshoppe triple chocolate filled gourmet cupcakes 11.7 oz. UPC 7 70981 31001 5 and 7 70981 31116 6 Favorite Day Gourmet Triple Chocolate filled cupcakes 11.7 oz. UPC 0 85239 42017 1
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0292-2022·2021-12-29

    Kimberley's Bakeshoppe Christmas Cupcakes Recalled for Potential Metal Contamination

    GIVE AND GO is recalling Kimberley's Bakeshoppe Christmas cupcakes with rings (22 oz.) due to potential metal in the product. The recall affects approximately 1.14 million units distributed nationwide.

    Product
    Kimberley's bakeshoppe Christmas cupcakes with rings 22 oz. UPC 7 70981 31188 3
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0395-2022·2021-12-29

    VirtuTRAX Instrument Navigator Sensor May Fail to Tighten

    Civco Medical recalls VirtuTRAX Instrument Navigator sensors that may fail to tighten onto instruments during use. No injuries reported.

    Product
    VirtuTRAX Instrument Navigator, Sensor with 14 Ga VirtutTRAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0287-2022·2021-12-29

    Medline Hand Sanitizer Foam Recalled for Defective Containers

    Medline Industries Inc is recalling Hand Sanitizer Foam in multiple sizes due to leaking bottles and dispensing issues reported by customers. The product was distributed nationwide and internationally.

    Product
    Hand Sanitizer Foam (ethyl alcohol), 62% v/v, packaged in a) 1.5 Oz. cans, NDC 53329-970-12; b) 8 Oz. (227 g) cans, NDC 53329-970-08; and c) 16 Oz. (453 g) cans, NDC 53329-970-06; Manufactured for: Medline Industries, Inc., Northfield, IL 60093.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0396-2022·2021-12-29

    VirtuTRAX Instrument Navigator recalled for potential tightening failure

    Civco Medical Instruments is recalling VirtuTRAX Instrument Navigator devices due to a potential defect that may prevent proper tightening onto medical instruments. The device was distributed worldwide.

    Product
    VirtuTRAX Instrument Navigator, 14 Ga VirtuTRAX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0316-2022·2021-12-29

    Kimberley's Bakeshoppe Sugar Cookies Recalled for Potential Metal Contamination

    GIVE AND GO is recalling Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies (9.4 oz., UPC 7 70981 30312 3) nationwide due to potential metal in the product.

    Product
    Kimberley's bakeshoppe vanilla mini Frosted soft Sugar Cookies 9.4 oz. UPC 7 70981 30312 3
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0309-2022·2021-12-29

    Freshness Guaranteed Black Forest Tiny Pies recalled for potential metal contamination

    Freshness Guaranteed Black Forest Tiny Pies 18.5 oz. are being recalled nationwide due to potential metal in the product. Consumers should not eat the product and should contact the manufacturer or retailer.

    Product
    Freshness Guaranteed Black Forest Tiny Pies 18.5 oz. UPC 0 78742 37635 6
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0294-2022·2021-12-29

    Penicillin V Potassium Oral Solution recalled for subpotency

    Teva Pharmaceuticals USA is recalling certain lots of Penicillin V Potassium for Oral Solution nationwide because the medication is subpotent—containing less active ingredient than labeled. The recall affects 100 mL and 200 mL bottles distributed nationwide.

    Product
    Penicillin V Potassium for Oral Solution, USP 125 mg (200,000 U) per 5 mL a) 100 mL (NDC 00093-4125-73) and b) 200 mL (NDC 00093-4125-74) (when mixed) bottles, Rx Only, Manufactured For: Teva Pharmaceuticals USA, Inc. North Wales, PA 19454
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0290-2022·2021-12-29

    Cupcakes Recalled Due to Potential Metal Contamination

    Give and Go is recalling multiple cupcake products totaling approximately 1.14 million units due to potential metal contamination. Affected products were distributed nationwide.

    Product
    two-bite vanilla & chocolate cupcakes 10 oz. UPC 7 70981 04502 3 20 oz. UPC 7 70981 03107 1 meijer mini assorted cupcakes with Holiday inspired sprinkle blend 20 oz. UPC 7 08820 40243 0 Kimberley's bakeshoppe vanilla & chocolate cupcakes 22 oz. UPC 7 70981 31122 7
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0413-2022·2021-12-29

    Testicular Prosthesis Recalled Due to Incorrect Size Labeling

    Coloplast Manufacturing is recalling Torosa Saline-Filled Testicular Prosthesis (Size Small) due to incorrect size labeling. Nineteen units were distributed in the US and Canada.

    Product
    Torosa Saline-Filled Testicular Prosthesis (Size Small)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0289-2022·2021-12-29

    Fexofenadine Hydrochloride Tablets 60 mg Recalled for Failed Impurities and Degradation Specifications

    The Harvard Drug Group is recalling Fexofenadine Hydrochloride Tablets, 60 mg, distributed by Major Pharmaceuticals nationwide due to failed impurities and degradation specifications. Affected lots are H00005, H00006, and H00007.

    Product
    Fexofenadine Hydrochloride Tablets, 60 mg, 500 Tablets per bottle, Distributed by: Major Pharmaceuticals, 17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 NDC 0904-6979-40
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0404-2022·2021-12-29

    Stanbio TDM/B-Hydroxybutyrate Controls Recalled Due to Improper Storage Temperature

    Medline Industries is recalling Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls due to improper storage conditions. The product was shipped at room temperature instead of the required refrigerated environment.

    Product
    Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateCPSC·22042·2021-12-29

    American Angler Electric Fillet Knives Recalled for Laceration Hazard

    Scott Fetzer Consumer Brands is recalling about 43,200 American Angler Electric Fillet Knives because the trigger mechanism can become stuck in the "on" position, posing a laceration hazard to users.

    Product
    American Angler Electric Fillet Knives
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V00M000·2021-12-28

    Hyundai recalls vehicles for windshield detachment risk in Santa Fe and other models

    Hyundai is recalling certain 2020-2021 Santa Fe, 2021 Sonata, and Elantra vehicles due to improper windshield bonding that may cause detachment during a crash. Dealers will reinstall windshields at no cost.

    Product
    HYUNDAI — HYUNDAI SANTA FE, SONATA, ELANTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00K000·2021-12-28

    2022 Hyundai Santa Fe instrument cluster display may invert upon startup

    Hyundai is recalling certain 2022 Santa Fe PHEV and HEV vehicles because the instrument cluster display may invert upon startup, making it illegible and preventing drivers from seeing speed and safety warnings.

    Product
    HYUNDAI — HYUNDAI SANTA FE PLUG-IN HYBRID, SANTA FE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V00J000·2021-12-27

    Mercedes-Benz Recalls 2022 EQS and S-Class for eCall Software Defect

    Mercedes-Benz is recalling 2022 EQS 450, S 500, and S 580 vehicles because a software defect may disable the emergency call system, potentially delaying emergency response.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 450, S 500 4MATIC, S 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22714·2021-12-23

    Polaris RZR and GENERAL Recreational Off-Road Vehicles Steering Wheel Separation Recall

    Polaris is recalling about 8,800 RZR and GENERAL recreational off-road vehicles because the steering wheel can separate, causing loss of control and crash risk. Polaris has received 33 reports of broken or cracked steering wheel spokes, including five rollovers and two injuries.

    Product
    Polaris RZR and GENERAL Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide