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 48,122 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

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)

Medical devices

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)

Food

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)

Meat & poultry

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

Medical devices

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)

Medical devices

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)

Drugs

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Food

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)

Food

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)

Food

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)

Food

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)

Medical devices

Reported May 18, 2016

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…

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

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom Unite Connect for Nurse Call (version 2.2.0).

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

Ascom US, Inc.

FDA (openFDA device enforcement)

Food

Reported May 18, 2016

Bertagni fresh Sweet Butternut Squash Ravioli, packaged in a paper tray inside a plastic bag and wrapped around with…

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

Bertagni 1882

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2016

Axial Torque Limiting Driver (1st generation) Product Usage: The Bradshaw Medical Axial Torque Limiting Driver is a…

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

Bradshaw Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Food

Reported May 18, 2016

Raw Meal Organic Vanilla Powder; Organic Shake and Meal Replacement; 949 g, 475 g, and 10-ct tray (68 g each). Packaged…

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

Garden Of Life LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 18, 2016

Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…

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

Medtronic

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2016

TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage:…

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

Applied Medical Technology Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 11, 2016

Emerald 100 Calorie Packs of Cashew Halves & Pieces, roasted and salted. 7 pack/ 0.62 oz. each (17.5 g). Ingredients:…

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

Diamond 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.