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.
4,310 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Indiana too — those are in the archive.
Reported Jun 8, 2016
Hip Preservation System Signature Series PreBent Burs under the following labels: 1) PreBent Spherical Bur, 5.5mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConMed Corporation
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Walnut Delights 6 Pack Net Weight: 9 oz. PLU #69690 UPC: 2 69690 20399 7 Giant Eagle, LLC, Pittsburgh, PA
High riskUsing this product could cause serious injury, illness or death — stop using it now.Giant Eagle, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Torque Limiting Handle: PRECIMED, T-Handle Torque, Non Sterile. Handle: Customer Number/Model: MCL120014 T14000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Greatbatch Medical
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Integra MicroFrance Monopolar and Bipolar Electrosurgical Instruments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Novocastr Liquid Mouse Monoclonal Antibody Renal Cell Carcinoma Marker (RCC) is recommended for use as part of a panel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Angel Wings Complete Daily Multi with 146 nutrients including Anti-aging and Superfruit Antioxidants and 75 Plant…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Liquid Assets Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
CADD Administration Sets with Flow Stop, Product Reorder No: 21-7321-01, 21-7321-24, 21-7322-01, 21-7322-24,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sterilmed, Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Kroger CRANBERRY DELIGHT TRAIL MIX NET WT 14 OZ INGREDIENTS: DRIED CRANBERRIES ***ALMONDS, SUNFLOWER SEEDS*** UPC 0…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Kroger Co.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 3, 2016
Butterfield Foods, LLC. Recalls Broccoli Salad Kit Products Due To Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Butterfield Foods, LLC
USDA FSIS
Reported Jun 1, 2016
WHIN Infusion Set - 90 Huber Needle and Wing (22 ga/1in). Intravenous delivery through intravascular ports, 20 units…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
FDA (openFDA device enforcement)
Reported Jun 1, 2016
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Morphine Sulfate 0.5 mg/mL, Preservative Free in 0.9% Sodium Chloride, Rx, total volume 1 mL, This is a compounded…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Pharmakon Pharmaceuticals
FDA (openFDA drug enforcement)
Reported Jun 1, 2016
Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument.
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 Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
THE SAUSAGE MAKER SEASONING Dried Sausage Sticks under the following labels: 1) Net Wt 6.5 oz, 2) Net Wt 2 lbs, 3) Net…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Sausage Maker, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 25, 2016
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamedix Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported May 25, 2016
Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Msu Dept Of Fd Sci Dairy Plant
FDA (openFDA food enforcement)
Reported May 25, 2016
Phosphoric Acid, 75% and 85% Food Grade (Brand Name PRAYPHOS PPA 75% FG and PRAYPHOS PPA 85% FG)
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Prayon Inc.
FDA (openFDA food enforcement)
Reported May 25, 2016
Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 25, 2016
COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unfi
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.