All recall categories

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 48,132 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Mar 27, 2013

Variable Angle Locking Compression Plate/VA-LCP Dorsal Distal Radius Plate, Part Number 02.115.431. Indicated for:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Synthes USA HQ, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 27, 2013

Dannon Activia LIGHT Nonfat Yogurt Peach Flavor 4x4oz cups INGREDIENTS: CULTURED GRADE A NONFAT MILK, WATER, PEACHES…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

The Dannon Company, Inc. - Discovery & Innovation Center

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 27, 2013

Vascular Solutions, Inc., Guardian II and Guardian II NC Hemostasis Valve, used in cardiopulmonary bypass. Model…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Vascular Solutions, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2013

55613210946 Western Family, Easy Sides, Herb & Butter Pene, Net WT 5.5 oz (156 g), UPC "0 15400 12655 7", Proudly…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bay Valley Foods LLC/ TreeHouse Foods, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 20, 2013

10021 Roman Meal Premium Oat Bran Mix ( Oat Flour, Oats, Oat Bran, white Wheat Bran, Red Wheat Bran, Stabilizi....,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Dakota Specialty Milling, Inc.

51 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 20, 2013

GE Healthcare, Innova 2100 IQ, Innova 3100 IQ, Innova 4100 IQ. Cardiovascular X-ray imaging systems. For use in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2013

Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: G71200 Genesis implant for single stage or two stage…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Keystone Dental Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 20, 2013

Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 20, 2013

Wildcat Creek Farms Country Style Butter Flavored Popcorn Salt, 4.5oz glass shaker, UPC 7 28123 91010 4 & 40 oz pete…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Wildcat Creek Popcorn

FDA (openFDA food enforcement)

Food

Reported Mar 13, 2013

Food Club(R) MEXICAN STYLE ENCHILADA SAUCE, RED, NET WT 10 OZ (284g), DISTRIBUTED BY TOPCO ASSOCIATES LLC, 7711 GROSS…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bruce Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2013

PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 13, 2013

GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume Viewer 3.x (Advantage Workstation 4.1) Volume…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

Food

Reported Mar 13, 2013

Chocolate bridge mix in 10 oz, 3 oz, and 3.5 oz bags

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Gorant Candies Inc. A Division

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2013

Philips Medical System Extended Brilliance Workspace (EBW), Computed Tomography X-Ray System. The Extended Brilliance…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 13, 2013

ALL NATURAL ANCIENT GRAIN BREAD, NET WT. 13.8 OZ. (393 g), PRODUCT OF CANADA, UPC 0 49800 08712 5 (appears on bag),…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Rich Products Corp.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2013

AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2013

Aesculap Bipolar Generator Foot Pedal, Catalog No. GK226, for electrosurgical cutting and coagulation.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Aesculap, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2013

Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems (Cleveland) Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2013

Stryker XIA 3 Iliac Screwdriver, 3-PCS. The XIA 3 Iliac Screwdriver is used to drive XIA 3 closed head Monoaxial and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Spine

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Animas Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ansell Healthcare Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2013

MAYFIELD¿ Composite Series Base Unit Standard, Model (A3101), Rx ONLY, Integra LifeScience Corporation, 4900 Charlemar…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Food

Reported Feb 27, 2013

Lean Cuisine Culinary Collection Mushroom Mezzaluna Ravioli ravioli filled with portobello & button mushrooms, romano &…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle USA

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.