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.

Which agencies issued them

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.

45101–45125 of 83415

  • LowFDA (Drugs)·D-0219-2018·2018-01-24

    Shionogi Recalls Mefenamic Acid Capsules Due to Foreign Particles

    Shionogi Inc. is recalling 968 bottles of Mefenamic Acid Capsules, 250 mg, due to the presence of black particles found during routine stability testing.

    Product
    Mefenamic Acid Capsules, USP, 250 mg, 30-count bottle, Rx only, Distributed by Prasco Laboratories, Mason, OH 45040, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ 07981, NDC 66993-070-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V064000·2018-01-22

    Suzuki Recalls 2017-2018 GSX-R1000 Motorcycles for Chain Break Risk

    Suzuki is recalling 2017-2018 GSX-R1000 motorcycles because a gear shift error can cause the drive chain to break, leading to power loss and crash risk.

    Product
    SUZUKI — SUZUKI GSX-R1000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V060000·2018-01-22

    Wayfarer Recalls 2017 24 QW RVs for Defective Fire Extinguishers

    Wayfarer is recalling 2017 24 QW recreational vehicles because the installed Kidde fire extinguishers may clog or detach, potentially failing to function during a fire.

    Product
    WAYFARER — WAYFARER 24 QW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V066000·2018-01-22

    Forest River Recalls 2018 Cherokee Trailers for Lighting Defects

    Forest River is recalling 2018 Cherokee recreational trailers because side marker lights are improperly positioned and reflectors may be missing, reducing visibility.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V065000·2018-01-19

    Aston Martin Recalls 2017-2018 DB11 Vehicles for Air Bag Defect

    Aston Martin is recalling 2017-2018 DB11 V12 and V8 Coupe vehicles because the driver's frontal air bag may deploy unexpectedly due to insufficient grounding.

    Product
    ASTON MARTIN — ASTON MARTIN DB11
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V062000·2018-01-19

    Newmar Recalls 2017-2018 Motorhomes Due to Headlight Visibility Defect

    Newmar is recalling 2017-2018 Ventana and Dutch Star motorhomes because low beam headlights do not illuminate with high beams, reducing visibility.

    Product
    NEWMAR — NEWMAR VENTANA, DUTCH STAR, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18081·2018-01-19

    Panasonic Recalls 55-Inch Televisions and Swivel Stands Due to Tip-Over Hazard

    Panasonic is recalling 55-inch flat screen televisions with tabletop swivel stands because the mounting screws can loosen, causing the TV to tip over and potentially injure or kill children.

    Product
    Panasonic 55-inch flat screen LED/LCD televisions with tabletop swivel stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·004-2018·2018-01-18

    Café Spice Recalls Chicken Salad Products Due to Undeclared Milk Allergen

    Café Spice GCT Inc. is recalling ready-to-eat chicken salad products because they contain milk, an undeclared allergen, and are mislabeled as chicken wraps.

    Product
    CAFE SPICE LLC — Café Spice GCT Inc., Recalls Ready-To-Eat Chicken Salad Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18080·2018-01-18

    Bed Bath & Beyond Recalls UGG Hudson Comforters Due to Mold Risk

    Bed Bath & Beyond is recalling UGG Hudson comforters due to a risk of mold exposure. Consumers should stop using the products and return them for a full refund.

    Product
    Hudson comforters by UGG
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18715·2018-01-18

    Hillsdale Furniture Recalls Bar Stools Due to Fall Hazard

    Hillsdale Furniture is recalling Polston and Collin bar stools because the seat can loosen or break off, posing a fall hazard. No injuries have been reported.

    Product
    Bar stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0566-2018·2018-01-17

    Nodine's Smokehouse Recalls Smoked Salmon Due to Listeria Risk

    Nodine's Smokehouse Inc. is recalling smoked salmon packages nationwide due to potential Listeria monocytogenes contamination.

    Product
    Smoked salmon in 1.5 oz. and 8 oz. packages
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0638-2018·2018-01-17

    Jack Brown Produce Recalls Fuji Apples for Listeria Contamination Risk

    Jack Brown Produce is voluntarily recalling Fuji apples due to potential Listeria monocytogenes contamination reported by a supplier.

    Product
    Fuji, whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0639-2018·2018-01-17

    Jack Brown Produce Recalls Golden Delicious Apples Due to Listeria Risk

    Jack Brown Produce is voluntarily recalling Golden Delicious apples due to potential Listeria monocytogenes contamination. The recall affects specific lots distributed in five US states.

    Product
    Golden Delicious whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-0208-2018·2018-01-17

    Teva Recalls Moexipril Hydrochloride Tablets Due to Impurity Test Failure

    Teva Pharmaceuticals is recalling specific bottles of Moexipril Hydrochloride and Hydrochlorothiazide tablets because routine stability testing found high levels of a degradation impurity.

    Product
    Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0640-2018·2018-01-17

    Jack Brown Produce Recalls Apples Due to Listeria Risk

    Jack Brown Produce is voluntarily recalling multiple varieties of apples because they may be contaminated with Listeria monocytogenes.

    Product
    Golden Del., Gala, Fuji, Honey Crisp; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0637-2018·2018-01-17

    Jack Brown Produce Recalls Gala Apples Due to Listeria Risk

    Jack Brown Produce is voluntarily recalling specific lots of Gala apples due to potential Listeria monocytogenes contamination.

    Product
    Gala, whole fresh apples; Metric Tray sizes, 50ct, 55ct, 60ct, 78ct, 113ct, 2# Poly bags, 3# Poly bags and 5# Mesh bags; Trays-113ct (5trays per case), 55, 60, 78ct (2trays per RPC case) 2# & 3# - 12 bags per case, 5# - 8 bags per case
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0322-2018·2018-01-17

    CareFusion Recalls Alaris Syringe Pumps Due to Plunger Gripper Failure

    CareFusion is recalling Alaris Syringe Pump Model 8110 units because the syringe plunger grippers may fail to close automatically, potentially affecting medication delivery.

    Product
    Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pump module and Alaris PCA module are infusion pump modules for the Alaris System. The syringe pump and PCA pump delivers medication or fluids in a manner similar to current syringe…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0324-2018·2018-01-17

    Cordis S.M.A.R.T. Flex Biliary Stent System Recalled for Cracked Luer Hubs

    Cordis Corporation is recalling 511 units of the S.M.A.R.T. Flex Biliary Stent System due to a potential for cracked luer hubs.

    Product
    Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictures in the biliary tree.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0258-2018·2018-01-17

    Orthoscan Mobile Mini C-arm System Recalled for Software Defect

    Orthoscan is recalling Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.

    Product
    Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0259-2018·2018-01-17

    Orthoscan Mobile Mini C-arm System Recalled for Software Defect

    Orthoscan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than is visible to the user.

    Product
    Mobile Mini C-arm system Part # 1000-0004. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0321-2018·2018-01-17

    Ambu Universal Flex2 Breathing Circuits Recalled for Leak Test Failures

    King Systems Corp. dba Ambu, Inc. is recalling 871,116 Universal Flex2 Breathing Circuits due to potential leak test failures.

    Product
    UNIVERSAL FLEX2 BREATHING CIRCUIT, Item Numbers: D460-6133Z, D390-6121Z, D390-6121Z, D495-61Z, DF4116-6121Z, D466-61Z, DFP170-6121, DF3115-6121Z, DF375-6121Z, DF3115-6121Z, DF3115-6121Z, D360-8031Z, D465-61Z, JD365-6033Z, DF370-6121Z, DF3110-61Z, DF375-17621Z, DF375-6121Z…
    Category
    Medical Device
    Distribution
    43 states
  • HighFDA (Devices)·Z-0261-2018·2018-01-17

    OrthoScan Recalls Mobile Mini C-arm Systems Due to Software Defect

    OrthoScan is recalling 2,012 Mobile Mini C-arm systems because a software defect allows users to activate Digital Zoom during live imaging, exposing a larger x-ray field than visible.

    Product
    Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide