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.
Reported Oct 21, 2015
TASTEE Plain Caramel Apple, www.tasteeapple.com NET WT. 3 OZ 85g 0 35266 00027 3 "THIS PRODUCT CONTAINS THE FOLLOWING…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tastee Apple Inc.
FDA (openFDA food enforcement)
Reported Oct 14, 2015
Caribou Chocolate Chip Toffee Pecan Biscotti, Net Wt. 1.4 oz. (40g) in clear cello flow wrap bag.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Caribou Coffee Company Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 14, 2015
Specialist 2 Intramedullary (SP2 IM) Rod 400mm Instrument (PN 96-6120) The SP2 IM Rod 400mm Instrument (PN 96-6120) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2015
Monaco Radiation Treatment Planning System. Used to make treatment plans for patients with prescriptions for external…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Oct 14, 2015
Centricity PACS IW by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare
FDA (openFDA device enforcement)
Reported Oct 14, 2015
organic girl - good clean greens baby spinach - tender nutrition baby leaves. Washed 3 times. USDA Organic. 5 oz..…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NewStar Fresh Foods, LLC
FDA (openFDA food enforcement)
Reported Oct 7, 2015
Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferno-Washington Inc.
FDA (openFDA device enforcement)
Reported Oct 7, 2015
Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
Reported Oct 7, 2015
Imperial Sugar, Pure Granulated Sugar, Net wt. 50 lbs (22.6 kg), Distributed by Imperial-Savannah LP, Sugar Land, Texas…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Savannah-Imperial LP- Savannah Sugar Refinery
7 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 7, 2015
Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
The Leica ASP6025 Tissue Processor. Pathology and Hematology Departments. The Leica ASP6025 Tissue Processor is an…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2015
Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each bar)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sam MillsUSA LLC
FDA (openFDA food enforcement)
Reported Sep 23, 2015
KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellbran Candies and Snacks Inc.
FDA (openFDA food enforcement)
Reported Sep 23, 2015
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2015
NICO Myriad Console Model number NN-7000 The Myriad System is a surgical system specifically designed for morcellation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nico Corp.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
IQF Red Tart Cherries, 30 lbs., 2/5 lb packages/case, 4/5 lb. packages per case; packed in cartons, square plastic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coloma Frozen Foods, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 16, 2015
Black Currant Huckleberry, Brioche and Jam Ice Cream Bucket, 313, Jeni's Splendid Ice Creams, LLC, 3 gallons, plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
133 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 16, 2015
MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent; SMN 10316877. Used to prepare the Red Blood Cell hemolysate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 16, 2015
2.4, 3.0, and 4.0 mm Gridlock Screw Driver Bit, Model Number 310-30-003, Lot Number TSL002605, NON-STERILE. For use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
FIRMap 60mm Catheter; Size: 60 mm; Length 50.4 inches French Size Diameter: 8.5F (2.84mm) Model number : USAR064060…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Electrophysiology
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Golden Seal Extract packaged in 1 FL OZ (29mL) droppers. HoneyCombs Industries, 10671 6075 Road, Montrose, CO 81403.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HoneyCombs Industries, LLC
6 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 9, 2015
Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Indiana recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.