Recalls distributed in Indiana
These notices name Indiana in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.
4,253 stored notices name Indiana, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Feb 23, 2022
RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a component of the following catalog numbers of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Base 10 Genetics Inc.
FDA (openFDA device enforcement)
Reported Feb 23, 2022
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
Reported Feb 18, 2022
Corfu Foods, Inc. Recalls Swai (Siluriformes) Products Imported Without Benefit of Import Reinspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Corfu Foods, Inc.
USDA FSIS
Reported Feb 16, 2022
Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amys Kitchen Inc.
FDA (openFDA food enforcement)
Reported Feb 16, 2022
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Feb 16, 2022
Wishbone Thousand Island Dressing 15oz. bottle UPC 0-41321-00645-6 and 24 oz. bottle UPC 0-41321-00731-6; six bottles…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Conagra Brands
1 more product in this recall
FDA (openFDA food enforcement)
Reported Feb 16, 2022
Ahold 10oz Chopped Romaine Product UPC 688267011085
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
75 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 16, 2022
Natural Way Cheese Chive Cheese Curds, retail 12oz plastic bag UPC 8 10056 75107 4, 12 retail units per wholesale case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natural Way Cheese
10 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 9, 2022
OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abiomed, Inc.
FDA (openFDA device enforcement)
Reported Feb 9, 2022
CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY, IMMY, Lateral Flow Assay for the Detection of Cryptococcal Antigen in serum…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Immuno-Mycologics, Inc.
FDA (openFDA device enforcement)
Reported Feb 9, 2022
Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LivaNova USA, Inc.
FDA (openFDA device enforcement)
Reported Feb 9, 2022
ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Feb 2, 2022
Brownie Points Schmurtle 2oz Packaged in food grade cellophane only used as gift basket filler - not sold individually
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brownie Points LLC
FDA (openFDA food enforcement)
Reported Feb 2, 2022
"5- Lettuce Mix" (salad product) packed in 6oz. packages
High riskUsing this product could cause serious injury, illness or death — stop using it now.Fresh Express Inc. (Div
89 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 2, 2022
GE Vscan Extend, being sold as "Vscan Extend Console"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 2, 2022
GAT SPORT JETFUEL DIURETIC; FOR RELIEF OF WATER WEIGHT GAIN; Muscle Defining Formula; Stimulant Free Natural Herbal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.World Health Products LLC
FDA (openFDA food enforcement)
Reported Jan 26, 2022
Gentueri Viral Transport Medium (VTM), Sterile, IVD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gentueri Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
VITROS Immunodiagnostic Products High Sample Diluent A Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jan 26, 2022
1. Sensis, material # 10764561; UDI: 04056869010137 2. Sensis Vibe Hemo, material # 11007641; UDI: 04056869010199 3.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Jan 19, 2022
OCT-Camera 211 01 A1, Running software iOCT-Control 3 v1.4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Haag-Streit USA Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Proteus 235; Version: PTS-8 versions before PTS-8.7.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ion Beam Applications S.A.
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Ki Mobility, Little Wave Tyke (Weight Limit: 95 lbs), Specifically the IFU The Little Wave Tyke is a manually operated…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ki Mobility LLC
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Medtronic Custom Perfusion kits, with the following product descriptions and corresponding model numbers: 1. CUSTOM…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
FDA (openFDA device enforcement)
Reported Jan 19, 2022
Boba Origin Brown-Sugar Milk Tea 100% WHEY PROTEIN ISOLATE 5.5g BCAA INGREDIENTS: Whey Protein Isolate, Black Tea,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.NutraCap Labs LLC
105 more products in this recall
FDA (openFDA food enforcement)
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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.