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.
4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Mar 13, 2019
DG Baby Gripe Water herbal supplement with organic ginger and fennel extracts, 4 FL OZ (120 mL) Liquid Dietary…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kingston Pharma LLC
FDA (openFDA food enforcement)
Reported Mar 13, 2019
Cepheid Respiratory Control Panel Catalog #8199 for in vitro diagnostic use
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Raindrop Near Vision Inlay, REF: RD1-1, Sterile, Rx Only, Manufacturer ReVision Optics, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Rvo 2.0, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2019
Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research Laboratories Ltd.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Phoenix AST-s Indicator, Catalog Number 246009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.King Orchards
FDA (openFDA food enforcement)
Reported Mar 6, 2019
Draco Enzymatic Deep-Cleaning Pads, Product Number HY0305Z Product Usage: Multi-tiered enzymatic detergent contains…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Madison Polymeric Engineering
FDA (openFDA device enforcement)
Reported Mar 6, 2019
The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2019
BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems USA Com
FDA (openFDA device enforcement)
Reported Mar 6, 2019
Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet Spine Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2019
Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 20, 2019
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AtriCure, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Chicago Bar Company LLC Rxbar
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cincinnati Sub-Zero Products LLC, a Gentherm Company
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Diamond Crystal Brands, Inc.
10 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2019
Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Oskri Corp.
19 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 20, 2019
Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PBM Nutritionals, LLC
FDA (openFDA food enforcement)
Reported Feb 13, 2019
ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Ireland Diagnostics Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature Sensing Infection Control Foley Catheter with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 13, 2019
Gold Medal Unbleached All Purpose Flour. Net Wt 5 lb. (2.26kg). UPC 16000-19610. Distributed By General Mills Sales,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
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.