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 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Nov 2, 2016
4205 Journey Rolling Walker Product Usage: used to assist people in walking
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nova Ortho-Med Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
ex-TEM Assay for ROTEM delta Thromboelastometry System. Art. no.: 503-05 US, ex-tem. Used to monitor the coagulation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TEM Systems Inc.
FDA (openFDA device enforcement)
Reported Nov 2, 2016
Neptune Plus (Hemostatic Pad), Part Numbers: 8870-03 Neptune Pad is used to promote the rapid control of bleeding and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TZ Medical, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Awareness Corporation
FDA (openFDA food enforcement)
Reported Oct 26, 2016
HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
COZY SHRIMP, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kabobs Inc.
26 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Hillcrest Farms Poultry Gravy Mix in 25lb brown poly-lined bags
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.National Foods Packaging Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
Nature's One, Organic PediaSmart¿ Dairy Vanilla complete nutrition beverage for kids 1 to 13 years NET WT 12.7 oz (360…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natures One Inc.
FDA (openFDA food enforcement)
Reported Oct 26, 2016
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Oct 26, 2016
FI Dry Blueberry / Strawberry Blend, Product Code 21585. 40 lb corrugated case with polyliner. Manufactured by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.QualiTech, Inc.
17 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 26, 2016
RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
FDA (openFDA device enforcement)
Reported Oct 26, 2016
25 gauge VersaVit 2.0 Core Essentials Procedure Pack, Product/Part Number 70025E, packaged in HIPS rigid tray with a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synergetics Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 26, 2016
LipiFlow thermal Pulsation System, consisting of Console and Activator, Model LFD-1100 The LipiFlow Thermal Pulsation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tearscience, Inc.
FDA (openFDA device enforcement)
Reported Oct 26, 2016
Calix P PEEK Lumbar System, PLIF Rasp
Moderate riskThis product could cause temporary or reversible health problems — stop using it.X Spine Systems Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic Use- Sterile Single Use Only. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Banyan Medical, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
TheraSphere(R) YTTRIUM-90 CLASS MICROSPHERE INJECTION TheraSphere¿ is indicated for radiation treatment or as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biocompatibles U.K., Ltd.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Introes Pocket Bougie is an endotracheal tube introducer. The device is an endotracheal tube introducer and it is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brathwaites Oliver Medical
FDA (openFDA device enforcement)
Reported Oct 19, 2016
The Better-Bladder With 14" ID tubing, ITEM BB14, STERILE, Measure pressure noninvasively in the extracorporeal circuit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Circulatory Technology Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter, REF/Catalog Number CS-023, STERILE, Rx Only Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Oct 19, 2016
HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.HeartWare, Inc.
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Kelloggs ¿ Eggo ¿ Nutri-Grain¿ Whole Wheat Waffles 12.3 oz (10 ct) retail carton 8, 12.3 oz retail cartons per case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellogg Company
FDA (openFDA food enforcement)
Reported Oct 19, 2016
The Medix NatalCare LX Intensive Care Incubator. Neonatal incubator. Item numbers: DMNCLX1; KITNC-STLX0003;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
FDA (openFDA device enforcement)
Reported Oct 19, 2016
ADVIA Centaur XPT Immunoassay System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 19, 2016
Taylor Farms Cranberry Walnut Salad; Salad kit for one: Baby Lettuce Blend, Feta Cheese, Flat Bread Chips, Dried…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Taylor Fresh Foods 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.