The Recall Desk

State

Indiana product recalls

73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25101–25125 of 83092

  • SevereNHTSA·21V947000·2021-12-08

    Audi SQ5 and Q5 recalled for water ingress into control module

    Volkswagen Group of America (Audi) is recalling certain 2018–2022 Audi Q5 and SQ5 vehicles. Water or liquid can seep into the gateway control module, causing sudden engine power loss and increasing crash risk.

    Product
    AUDI — AUDI Q5, SQ5, Q5 SPORTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0253-2022·2021-12-08

    Puratos Easy Satin Creme Cake Bag Recalled for Metal Contamination

    Puratos Corporation is recalling Easy Satin Creme Cake Bag 50# (Batch Number 10644902) due to possible contamination with metal foreign material. The affected product was distributed to domestic and international customers.

    Product
    Easy Satin Creme Cake Bag 50#. Material #4107811
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0236-2022·2021-12-08

    Tastykake Butterscotch Krimpets recalled for potential metal fragments

    Flowers Foods is recalling Tastykake Butterscotch Krimpets in multiple sizes due to the potential presence of small metal fragments in one of the ingredients. The product was distributed across 36 states.

    Product
    Tastykake Butterscotch Krimpets 24oz (12-2ct) UPC 0 25600 00396 1; 12oz (6-2ct) UPC 0 25600 00227 8 ; 3oz UPC 0 25600 00002 1 & 2oz, UPC 0 25600 00083 0
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0264-2022·2021-12-08

    Teg H/A Cream Cake Bag contaminated with metal foreign material

    Puratos Corporation is recalling Teg H/A Cream Cake Bag 50# (Batch Number 10730404) due to potential contamination with metal foreign material. The product was distributed to customers in multiple U.S. states and internationally.

    Product
    Teg H/A Cream Cake Bag 50# Material #4107840
    Category
    Food
    Distribution
    11 states
  • HighCPSC·22027·2021-12-08

    Mark of Fifth Avenue Children's Robes Recalled for Flammability Hazard

    Mark of Fifth Avenue children's robes do not meet federal flammability standards for sleepwear and pose a risk of burn injuries. About 10,000 units sold online at Amazon and Walmart from August 2019 through June 2021 are affected.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0237-2022·2021-12-08

    Tastykake Creme Filled Krimpets recalled for possible metal fragments

    Flowers Foods is recalling certain Tastykake Creme Filled Krimpets due to potential small metal fragments in an ingredient. The recall affects products distributed to 37 states.

    Product
    Tastykake Creme Filled Krimpets 14.25oz (6-2ct) UPC 0 25600 00355 8; 3.625oz (3ct) UPC 0 25600 08637 7
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0266-2022·2021-12-08

    Teg Satin Supreme Yogurt Creme Recalled for Metal Contamination

    Puratos Corporation is recalling Teg Satin Supreme Yogurt Creme (50 lb bags) due to potential contamination with metal fragments. The product was distributed to customers across multiple US states and internationally.

    Product
    Teg Satin Suprm Yogurt Creme Ck Bag 50#. Material #4107525
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0321-2022·2021-12-08

    Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss

    Boston Scientific is recalling Hurricane RX dilation balloons used in endoscopic biliary procedures due to pinhole defects causing pressure loss that may prolong treatment.

    Product
    HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0233-2022·2021-12-08

    Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes Recall for Metal Fragments

    Flowers Foods is recalling Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes due to potential small metal fragments in an ingredient. The recall affects products distributed across multiple states.

    Product
    Tastykake Buttercreme Iced Creme Filled Chocolate Cupcakes 14.25oz (6-2ct) box UPC 0 25600 00230 8 & 2.375oz package, UPC 0 25600 00004 5
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-0327-2022·2021-12-08

    FDA Recalls Hurricane RX Dilation Balloons for Pressure Failure Risk

    Boston Scientific is recalling Hurricane RX Dilation Balloons nationwide due to pinhole defects that cause pressure loss or failure to maintain pressure during endoscopic procedures.

    Product
    HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545960
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0331-2022·2021-12-08

    Siemens Dimension Vista 500 software issue affects test accuracy

    Siemens is recalling 1,326 Dimension Vista 500 diagnostic devices worldwide due to incorrect default hemolysis, icterus, and lipemia indices that may affect test result accuracy.

    Product
    Dimension Vista 500- In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10284473 (US) and 10488224 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0315-2022·2021-12-08

    INBONE Total Ankle System recalled for package-labeling mismatch

    Wright Medical Technology is recalling INBONE Total Ankle System implants because the package contents and package labeling do not match.

    Product
    INBONE Total Ankle System, INBONE POLY INSERT SZ 2 10mm SULCUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0259-2022·2021-12-08

    Shirley's Choc Whoopie Pie Base recalled for metal contamination

    Puratos Corporation is recalling Shirley's Choc Whoopie Pie Base because the product may contain metal foreign material. Affected batches were distributed to customers in multiple U.S. states and internationally.

    Product
    Shirley's Choc Whoopie Pie Base MB Bg50#
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0261-2022·2021-12-08

    Shirley's Red Velvet WhoopiePie Recalled for Metal Contamination

    Puratos Corporation is recalling Shirley's Red Velvet WhoopiePie MB Bg 50# due to potential metal contamination. The product was distributed to customers across multiple U.S. states and foreign locations.

    Product
    Shirley's Red Velvet WhoopiePie MB Bg 50#. Material #4107554
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0234-2022·2021-12-08

    Tastykake Chocolate Cupcakes Recalled for Potential Metal Fragments

    Flowers Foods is recalling Tastykake Chocolate Cupcakes 12.75oz boxes due to the potential presence of small metal fragments in an ingredient. The product was distributed across 36 U.S. states.

    Product
    Tastykake Chocolate Cupcakes 12.75oz, UPC 0 25600 00219 3
    Category
    Food
    Distribution
    37 states
  • HighFDA (Devices)·Z-0320-2022·2021-12-08

    Boston Scientific Hurricane RX Dilation Balloons Recalled for Pressure Loss Defect

    Boston Scientific is recalling specific lots of Hurricane RX Dilation Balloons due to a pinhole defect that causes pressure loss, resulting in prolonged endoscopic procedures. Affected devices are used for dilating strictures in the bile duct.

    Product
    HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545890
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0322-2022·2021-12-08

    Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect

    Boston Scientific is recalling the Hurricane RX Dilation Balloon due to a pinhole defect causing pressure loss during endoscopic procedures. The defect may result in prolonged procedures and inability to effectively treat biliary strictures.

    Product
    HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:M00545910
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0238-2022·2021-12-08

    Tastykake Jelly Krimpets recalled for potential metal fragments

    Flowers Foods is recalling Tastykake Jelly Krimpets due to potential small metal fragments in an ingredient, as reported by a supplier. The recall affects 12oz and 3oz packages distributed across 37 US states.

    Product
    Tastykake Jelly Krimpets 12oz (6-2ct) UPC 0 25600 00228 5 & 3oz (3ct) UPC 0 25600 00025 0
    Category
    Food
    Distribution
    37 states
  • HighFDA (Food)·F-0256-2022·2021-12-08

    HEB Satin White Layer Cake Mix Recalled for Metal Contamination

    Puratos Corporation is recalling HEB Satin White Layer Cake in 50-pound bags due to possible contamination with metal foreign material. The affected product was distributed across multiple U.S. states and internationally.

    Product
    HEB Satin White Layer Cake Bag 50#. Material #4107393
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0330-2022·2021-12-08

    Dimension Vista 1500 Diagnostic Device: Incorrect HIL Index Defaults

    Siemens is recalling 1,407 Dimension Vista 1500 diagnostic devices worldwide due to incorrect default Hemolysis, Icterus, and Lipemia (HIL) index values affecting five assays.

    Product
    Dimension Vista 1500 In-vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluid SMN: 10444801(US) and 10444802 (OUS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0246-2022·2021-12-08

    UV-C Germicidal Wand Recalled for Excessive Ultraviolet-C Radiation

    MAX LUX CORP is recalling approximately 9900 handheld UV-C germicidal wands (Safe-T Lite) distributed nationwide due to excessive ultraviolet-C radiation emissions.

    Product
    The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0242-2022·2021-12-08

    Target Good & Gather Mixed Berry Sparkling Water Recall for Unlabeled Sulfites

    Target Good & Gather Mixed Berry Sparkling Water in 8-packs is being recalled due to unlabeled sulfites. Keurig Dr Pepper discovered the issue after receiving complaints about off flavor and off aroma.

    Product
    Target Good & Gather Mixed Berry Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 11516 9, UPC outer Carton (8 pack): 0 85239 11345 5
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·22028·2021-12-08

    GE Appliances Recalls Free-Standing and Slide-In Ranges for Tip-Over Hazard

    GE Appliances is recalling approximately 132,000 free-standing and slide-in electric and gas ranges because they can tip over if a heavy object is placed on an open oven door and the anti-tip-over bracket is not securely installed, risking burn injuries.

    Product
    Free-Standing and Slide-In Electric and Gas Ranges
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0255-2022·2021-12-08

    Finesse Bag 25# Flour Product Recalled for Metal Contamination

    Puratos Corporation is recalling Finesse Bag 25# (Material #4107218, Batch Number 10644766) because the product may be contaminated with metal fragments. The product was distributed domestically and internationally.

    Product
    Finesse Bag 25#. Material #4107218
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0326-2022·2021-12-08

    Boston Scientific HURRICANE RX Dilation Balloon Recalled for Pressure Loss

    Boston Scientific is recalling HURRICANE RX Dilation Balloons due to a pinhole defect that causes pressure loss during endoscopic procedures. The device may fail to maintain necessary pressure, potentially prolonging procedures.

    Product
    HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950
    Category
    Medical Device
    Distribution
    Distributed nationwide