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.

25126–25150 of 83092

  • HighFDA (Food)·F-0241-2022·2021-12-08

    Target Good & Gather Coconut Pineapple Sparkling Water Recalled for Unlabeled Sulfites

    Keurig Dr Pepper is recalling Target Good & Gather Coconut Pineapple Sparkling Water because some cans contain unlabeled sulfites. The affected products were distributed nationwide.

    Product
    Target Good & Gather Coconut Pineapple Sparkling Water 8 pack of 12 oz. cans UPC can: 0 85239 04059 1, UPC outer carton (8 pack): 0 85239 03833 8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0312-2022·2021-12-08

    Blood Culture Identification Test Recalled Due to False Positive Risk

    BioFire Blood Culture Identification 2 (BCID2) diagnostic panels are being recalled due to increased risk of false positive Acinetobacter calcoaceticus-baumannii results caused by non-viable contamination in blood culture vials.

    Product
    BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147 UDI: 00815381020338 Blood Culture Catalog No./Description: 442023/BD BACTEC Plus Aerobic medium in plastic vials 442021/BD BACTEC Lytic Anaerobic medium in plastic vials 442192//BD BACTEC Plus Aerobic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0328-2022·2021-12-08

    Cholesterol test system recalled due to calibration failure

    RANDOX CHOL cholesterol test system is recalled due to a calibration defect that causes quality control results to be flagged as out of range. This could result in inaccurate cholesterol measurements in patient samples.

    Product
    RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol in plasma and serum REF: CH200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0318-2022·2021-12-08

    Blood collection devices recalled due to premature needle retraction

    Magnolia Medical Technologies is recalling Steripath Gen2 Blood Collection Systems due to an uptick in complaints of premature needle retraction during blood collection.

    Product
    The Steripath Gen2 Blood Collection System Model Number/Description 2700-21-EN / Steripath Gen2 Blood Collection System - 21G, Wide Neck 2700-23-EN / Steripath Gen2 Blood Collection System - 23G, Wide Neck 27BD-21-EN / Steripath Gen2 Blood Collection System - 21G, Long…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0239-2022·2021-12-08

    7UP Zero Sugar Lemon Lime Soda Recalled for Unlabeled Sulfites

    Keurig Dr Pepper is recalling 7UP Zero Sugar Lemon Lime Soda due to unlabeled sulfites detected after customer complaints about off flavor and aroma. The recall affects 9,152 cases distributed nationwide.

    Product
    7UP Zero Sugar Lemon Lime Soda 12 pack of 12 oz. can UPC Cardboard Wrap Code: 7800001181 UPC Can Code: 0780790
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0262-2022·2021-12-08

    Shirley's Sugar Top Muffin Base Recalled for Metal Contamination

    Puratos Corporation is recalling Shirley's Sugar Top Muffin Base (15,950 lbs) because the product may contain metal foreign material. The affected batches were distributed to customers in multiple U.S. states and internationally.

    Product
    Shirley's Sugar Top Muffin Bse MB Bag50#. Material #4107632
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0267-2022·2021-12-08

    Teg Satin Choc Creme Cake contaminated with metal fragments

    Puratos Corporation is recalling Teg Satin Choc Creme Cake (50 lb bags, Batch 10688839) due to possible contamination with metal. The product was distributed across multiple states and internationally.

    Product
    Teg Satin Choc Creme Cake Bag 50#. Material #4107220
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0317-2022·2021-12-08

    HALYARD STERLING ZERO Nitrile Exam Gloves Recall for Discoloration and Loss of Elasticity

    O&M Halyard is recalling HALYARD STERLING ZERO nitrile exam gloves in all sizes due to discoloration and loss of elasticity with aging, making the gloves difficult or impossible to don without tearing. Approximately 5.86 million gloves distributed worldwide are affected.

    Product
    HALYARD STERLING ZERO NITRILE POWDER-FREE EXAM GLOVES, Sizes XS, S, M, L, and XL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0257-2022·2021-12-08

    NSA Creme Cake Recall Due to Potential Metal Contamination

    Puratos Corporation is recalling NSA Creme Cake in 50-pound bags due to potential metal contamination. The product may pose a choking or injury hazard.

    Product
    NSA Creme Cake Bag 50#. Material #4107591
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0308-2022·2021-12-08

    Abbott HeartMate Touch System App may fail due to Bluetooth interference issue

    The Abbott HeartMate Touch Communication System may experience temporary app failure when nearby Bluetooth devices attempt connections. Once properly connected, the system functions normally.

    Product
    Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0260-2022·2021-12-08

    Shirley's Neutral Whoopie Pie Mix recalled for potential metal contamination

    Puratos Corporation is recalling Shirley's Neutral Whoopie Pie MB Bag 50# (Batch Number 10584012) due to potential metal contamination. Consumers should not use the product.

    Product
    Shirley's Neutral Whoopie Pie MB Bag 50#. Material #4107773
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0325-2022·2021-12-08

    Hurricane RX Dilation Balloon Recalled Due to Pinhole Defect Causing Pressure Loss

    Boston Scientific is recalling certain lots of the Hurricane RX Dilation Balloon due to a pinhole defect that causes loss of pressure or prevents the balloon from gaining or maintaining pressure during use, potentially prolonging medical procedures.

    Product
    HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545940
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0258-2022·2021-12-08

    One Step Neutral/Vanilla Mousse Contaminated with Foreign Metal Material

    Puratos Corporation is recalling One Step Neutral/Vanilla Mousse (Batch 10672511) due to potential contamination with metal fragments. Affected domestic and international customers should not use the product.

    Product
    One Step Neutral/Vanilla Mousse Bag 25#. Material #4107486
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0240-2022·2021-12-08

    Polar Black Cherry Premium Seltzer recalled for unlabeled sulfites

    Keurig Dr Pepper is recalling Polar Black Cherry Premium Seltzer 12-packs due to unlabeled sulfites. The recall affects 7,849 cases distributed nationwide with product code date 12/16/2022.

    Product
    Polar Black Cherry Premium Seltzer 12 pack of 12oz cans UPC Cardboard Wrap Code: 7153700228, UPC Can Code: 7153700110
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0323-2022·2021-12-08

    Boston Scientific HURRICANE RX Dilation Balloon Pressure Loss Recalled

    Boston Scientific is recalling HURRICANE RX Dilation Balloons across the US due to pinhole defects that cause pressure loss during endoscopic procedures. The defect may prolong procedures and affect patient safety.

    Product
    HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545920
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0252-2022·2021-12-08

    Dulcerio Sponge Cake Mix Recalled for Possible Metal Contamination

    Puratos Corporation is recalling Dulcerio Sponge Cake Mix Bag 40# (Batch Number 10644901) due to possible contamination with metal foreign material. The product was distributed to customers in multiple U.S. states and internationally.

    Product
    Dulcerio Sponge Cake Mix Bag 40#. Material #4107381
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0250-2022·2021-12-08

    Puratos TK014 Choc Creamie Powder Blend Recalled for Metal Contamination

    Puratos Corporation is recalling TK014 Choc Creamie Powder Blend in 40 lb. bags due to potential metal contamination. The affected product was distributed domestically and internationally.

    Product
    TK014 Choc Creamie Powder Blend Bag 40 lb. Item number 4107774
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0251-2022·2021-12-08

    Dom. Creme Ck Bag 50# Recall Due to Metal Contamination

    Puratos Corporation is recalling Dom. Creme Ck Bag 50# (Batch Number 10584006) due to possible contamination with metal fragments. The product was distributed domestically and to select foreign locations.

    Product
    Dom. Creme Ck Bag 50#. Material # 10584006
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0324-2022·2021-12-08

    Boston Scientific Hurricane RX Dilation Balloon Recalled for Pressure Loss Defect

    Boston Scientific is recalling the Hurricane RX Dilation Balloon nationwide due to a pinhole defect causing loss of pressure or failure to maintain pressure during endoscopic procedures used to treat biliary strictures.

    Product
    HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545930
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0329-2022·2021-12-08

    GE Centricity Medical Imaging Software May Display Incomplete Patient Studies

    GE Healthcare recalled versions of Centricity Universal Viewer Zero Footprint Client software due to a potential defect that could display incomplete patient imaging studies. No injuries have been reported.

    Product
    GE Centricity Universal Viewer Zero Footprint Client
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V948000·2021-12-08

    Carson Fun Runner Trailers Recalled for Potential Gas Leak Risk

    Carson is recalling 2018-2020 Fun Runner FC20 trailers because an overtightened bolt may damage the stove's o-ring, causing a gas leak that increases fire risk.

    Product
    CARSON — CARSON FUN RUNNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0263-2022·2021-12-08

    Teg Creme Cake Bags Recalled for Potential Metal Contamination

    Puratos Corporation is recalling Teg Creme Cake Bags (50 lb) because they may contain foreign metal material. The affected product was distributed to customers in multiple U.S. states and internationally.

    Product
    Teg Creme Cake Bag 50#. Material #4107664
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Devices)·Z-0319-2022·2021-12-08

    NUVASIVE PRECICE Limb Lengthening System: Updated Instructions Clarify Patient Selection

    NuVasive is updating instructions for the PRECICE limb lengthening implant system to clarify it is for patients 18 years or older weighing 50 lbs or more, with no more than two devices implanted at a time.

    Product
    NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System: Model Number/Item Number/Product Description: CPA1-000 PA0382-001 End Cap CPA2-000 PA1051-000 PACKAGED END CAP, 8.5/ 10.7MM, +0MM CPA2-005 PA1051-005 PACKAGED END CAP, 8.5/ 10.7MM, +5MM CPA2-010…
    Category
    Medical Device
    Distribution
    47 states
  • ModerateFDA (Food)·F-0254-2022·2021-12-08

    Easy Satin Supreme Creme Cake Bag contaminated with metal

    Puratos Corporation is recalling Easy Satin Supreme Creme Cake Bag 50# due to potential metal contamination. The affected product was distributed to bakery and food manufacturers in twelve U.S. states and two Caribbean countries.

    Product
    Easy Satin Supreme Creme Cake Bag 50#. Material #4107808
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Food)·F-0235-2022·2021-12-08

    Tastykake Chocolate Creme Filled Cupcakes Recalled for Metal Fragments

    Flowers Foods is recalling Tastykake Chocolate Creme Filled Cupcakes due to the potential presence of small metal fragments in an ingredient. The affected product has an "Enjoy By" date of December 14 or December 18.

    Product
    Tastykake Chocolate Creme Filled Cupcakes 14.25oz, UPC 0 25600 00223 0
    Category
    Food
    Distribution
    37 states