State

Indiana product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55776–55800 of 83431

HighFDA (Food)·F-0792-2016·2016-03-30
Nestle Recalls Stouffer's Vegetable Lasagna Due to Potential Glass Contamination
Nestle USA is recalling Stouffer's vegetable lasagna products due to the potential presence of glass pieces. Consumers should check their freezers for affected items.
Product
Stouffer's vegetable lasagna. Keep Frozen. Sold in the following sizes and UPC: 1. Party Size Net Wt. 96 oz (6 lb) 2.72kg UPC 13800-19002. 2. Net Wt. 10 1/2 oz (297g) UPC 13800-10323. 3. Family Size Net Wt. 37 1/2 oz (2 lbs. 5 1/2 oz) 1.06 kg, UPC 13800-55510. 4.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1197-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover 4.5OZ MIDSTREAM W/CASTILE TOWL Item Code: 24015 Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1221-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Castile soap towelettes in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover PREC PRM 14FR SILVER FLY TY Item Code: PP14XSD ¿ ¿¿ Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0793-2016·2016-03-30
Nestle Recalls Stouffer's Spinach Souffle Due to Potential Glass Contamination
Nestle is recalling Stouffer's spinach souffle products due to the potential presence of glass pieces. Consumers should check their freezers for the specific production codes listed.
Product
Stouffer's spinach souffle. Simple Dishes. Keep Frozen. Net Wt. 12 oz (340 g) UPC 13800-10585.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1215-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
The FDA is recalling Castile soap towelettes included in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover P400 UM 18FR SIL COUDE SECURE Item Code: P4P18CSDK Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1214-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
Aplicare Castile Soap towelettes included in Foley Trays and Mid stream specimen kits are being recalled because they are contaminated with bacteria.
Product
Covidien Dover P400 PREM U/M 18FR SIL COUDE CATH SECURE Item Code: P4P18CSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1245-2016·2016-03-30
Nidek RT-5100 and RT-3100 Refractors Recalled for Arm Malfunction
Nidek Inc is recalling RT-5100 and RT-3100 refractors because the Near Point Chart Arm may lower spontaneously, posing a risk of slight injury to the patient's face or nose.
Product
RT-5100 (Epic 5100) Refractor and RT 3100 Refractor: Product Usage: Instrument providing means of positioning spherical and cylindrical lenses, prisms and other optical devices in front of a subjects eye for purpose of determining refractive error and binocular functions.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1229-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
Covidien LLC is recalling Castile soap towelettes used in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover PREC PRM 18FR SILVER FLY TY Item Code: PP18XSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits because they are contaminated with bacteria.
Product
Covidien Dover P400 UM 16FR SIL COUDE SECURE Item Code: P4P16CSDK Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1210-2016·2016-03-30
Castile Soap Towelettes Recalled Due to Bacterial Contamination
The FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover P400 PREM U/M 16FR TMP SNS CSD Item Code: P4P16TSD Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1204-2016·2016-03-30
Recall of Bacteria-Contaminated Castile Soap Towelettes in Medical Kits
FDA is recalling Aplicare Castile Soap towelettes found in Foley trays and specimen kits due to bacterial contamination.
Product
Covidien Dover PREM U/M 14FR SIL FLY Item Code: P4P14SD P400 Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0785-2016·2016-03-30
Nestle Recalls DiGiorno, Lean Cuisine, and Stouffer's Products for Glass Contamination
Nestle is recalling specific DiGiorno, Lean Cuisine, and Stouffer's products due to the potential presence of glass pieces.
Product
DiGiorno Rising Crust Spinach and Mushroom Pizza, UPC 71921-00335, Keep Frozen. Net Wt. 30.3 oz (1 lb 14.3 oz) 858g
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1202-2016·2016-03-30
Recall of Contaminated Castile Soap Towelettes in Medical Kits
FDA is recalling specific lots of Castile soap towelettes used in medical kits due to bacterial contamination.
Product
Covidien Dover MIDSTREAM KIT RING CASTILE Item Code: 4090SA Castile soap towelettes are used to clean the genital area for male and female patients
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1239-2016·2016-03-30
CareFusion Recalls Alaris PC Infusion Pump Units Due to Power Supply Error
CareFusion is recalling 170 Alaris PC Unit Infusion Pump Model 8000 devices because a power supply component may cause system error codes.
Product
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1175-2016·2016-03-30
Toshiba DRAD-3000E Wireless System Recalled for Image Transmission Failure
Toshiba is recalling 28 DRAD-3000E FPD Wireless Systems because they fail to complete image transmission, resulting in no radiographic image.
Product
Toshiba DRAD-3000E FPD Wireless System Product Usage The DRAD-3000¿ is intended for use with the ceiling-suspended tube support, high voltage generator, and bucky stand or bucky table incorporating a fixed or detachable (portable) flat panel detector for radiography of the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1243-2016·2016-03-30
Siemens IMMULITE 2000 Estradiol Test Recalled Due to Faslodex Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Estradiol Test kits because the drug fulvestrant (Faslodex) may cause falsely elevated estradiol results.
Product
IMMULITE 2000 EstradiolTest Code E2 Catalog Number: L2KE22, L2KE22 (D), L2KE26, L2KE26 (D) SMN: 10381178, 10702833, 10381177, 10702834 Product Usage: For in vitro diagnostic use the IMMULITE¿2000 systems Analyzers- for the quantitative measurement of estradiol in serum, as…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1189-2016·2016-03-30
Zimmer Spine Universal Clamp System Recall for Updated Cleaning Instructions
Zimmer Spine is issuing a correction notice for the Universal Clamp System to provide updated cleaning and disinfecting instructions.
Product
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and helps reduce spinal deformities and fractures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0781-2016·2016-03-30
AstraZeneca Recalls Tudorza Pressair Inhalers Due to Defective Delivery System
AstraZeneca is recalling Tudorza Pressair inhalers because some units have actuation counters set to a number other than 60.
Product
Tudorza Pressair (aclindinium bromide inhalation powder), 400 mcg per actuation, 60 Metered Doses per Inhaler, Rx Only. Manufactured for: AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850. Manufactured by: Forest Laboratories, Ireland Limited, Dublin 17 Ireland. Product of…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1232-2016·2016-03-30
Siemens syngo X Workplace Medical Workstation Recalled for Segmentation Error
Siemens Medical Solutions USA is recalling six syngo X Workplace medical workstations because imported segmentation results appear mirrored, rendering them unusable for ablation procedures.
Product
syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication, and storage of medical images and data on exchange media. It is used for diagnostic image viewing and post processing during interventional procedures. .
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1240-2016·2016-03-30
Siemens Estradiol Test Recalled Due to Potential False Results
Siemens is recalling ADVIA Centaur Enhance Estradiol tests because the drug fulvestrant may cause falsely elevated results.
Product
Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889, 10491445, 10697757 Product Usage: For in vitro diagnostic use in the quantitative determination of estradiol in human serum and plasma (heparinized and EDTA) using the ADVIA Centaur¿, ADVIA…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1190-2016·2016-03-30
Zimmer Biomet Issues Correction Notice for Instinct Java System Cleaning Instructions
Zimmer Biomet is issuing a correction notice to provide updated cleaning and disinfecting instructions for the Instinct Java System and Universal Clamp System.
Product
Instinct¿ Java¿ System (IFU reference: 046WAN0000T) . Stabilizes one or more vertebral segments from the thoracic spine to the sacrum during the development of bone tissue.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1247-2016·2016-03-30
Neurotherm Curved Radiofrequency Cannula Recalled for Mislabeling
Neurotherm, Inc. is recalling 135 curved radiofrequency cannulas because straight needles were incorrectly labeled as curved.
Product
Neurotherm Curved Radiofrequency (RF) cannnula 10 cm 18 gauge, 10 mm active tip Model Number: C-1010-R-18 Product Usage: The device is a radiofrequency needle, used for the application of radiofrequency energy with as intended result, thermo coagulation of nervous tissue…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V176000·2016-03-29
Forest River Georgetown RVs Recalled for Missing Emergency Egress Window
Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.
Product
FOREST RIVER — FOREST RIVER GEORGETOWN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V175000·2016-03-29
Forest River Recalls 2013-2016 Puma Trailers for Tire Clearance Issue
Forest River is recalling 2013-2016 Puma recreational trailers because tires may contact the wheel well on bumps, risking tire damage and loss of control.
Product
FOREST RIVER — FOREST RIVER PUMA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V177000·2016-03-29
Terex Recalls 2011-2016 Aerial Devices Due to Inadequate Boom Tip Welds
Terex is recalling 2011-2016 aerial devices because inadequate welds at the boom tip may cause the platform to tilt unexpectedly, increasing the risk of user injury.
Product
TEREX — TEREX AERIAL DEVICES
Category
Vehicle
Distribution
Distributed nationwide