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 Jan 25, 2017
FPI Breaded Round Shrimp Tail-On 1001990, 12-8 oz. cartons per master case, Master case 6 lbs. (2.72 kg)
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Liner Foods, Inc.
FDA (openFDA food enforcement)
Reported Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
OPT Croutons is a synthetic bone substitute designed for the repair of bony defects and is made of pure beta-tricalcium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jan 18, 2017
In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brand Castle LLC
FDA (openFDA food enforcement)
Reported Jan 18, 2017
SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Medline E-Z Lubricating Jelly; Bacteriostatic. Water Soluble. Sterile. 2 FL OZ (59 ml). Product Usage: For medical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Ind
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Merge Eye Station f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Manufacturing Limited
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Bayside Seasoning, 2 lb plastic jar, product number 61497
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Piazza Produce, Inc.
23 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2017
Biograph mCT S(40)-3R, Material Number 10248668 The Siemens Biograph mCT and Biograph mCT Flow systems are combined…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2017
Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Sustainability Solutions
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 11, 2017
Derby City Vending Buffalo Chicken Sandwich Deli Selections Ingredients: Chicken***Ranch Cup; Pretzel bun***Lettuce,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Derby City Vending Inc.
FDA (openFDA food enforcement)
Reported Jan 11, 2017
AMERICAN CLASSIC SUB Net Wt 6.5 oz (184g) Smoked ham, deli style bologna, hard salami with American and Swiss cheese on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eby Brown Co.
9 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 11, 2017
Ashby's Sterling Peanut Butter Landslide Ice Cream, 3 gallon container, frozen
High riskUsing this product could cause serious injury, illness or death — stop using it now.House Of Flavors, Inc.
FDA (openFDA food enforcement)
Reported Jan 11, 2017
GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tepha Incorporated
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Innova 2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
12 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
Shimadzu X-ray TV System, Catalog No. SONIALVISION G4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shimadzu Medical Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2017
SOMATOM Scope, Computed tomography x-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
CyberKnife Robotic Radiosurgery Systems, models: G3, G4, VSI. Radiology: The CyberKnife Robotic Radiosurgery System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accuray Incorporated
FDA (openFDA device enforcement)
Reported Dec 28, 2016
BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Affinity Fusion" Oxygenator with Integrated Arterial Filter, Affinity Fusion cardiotomy/Venous Reservoir, Perfusion…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 28, 2016
Apple Orchard Crisp Apple Hard Cider Three packages sizes: ¿ Loose case = 24 12 oz bottles ¿ 12 pack = 12 12 oz…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Samuel Adams Brewery Co.
FDA (openFDA food enforcement)
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Other states
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.