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.

4,309 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,826 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Sep 6, 2017

Alere iScreen Dx Urine Drug Screen Card, 20 Drug Detection, Kit Contents include 26 individually pouched devices and 1…

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

Ameditech Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2017

UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 6, 2017

CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.

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

Gold Medal Products Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2017

iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…

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

Optovue, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 6, 2017

German chocolate cakes labeled as Schnucks Bakery Deluxe Petite Cake Chocolate Iced Yellow, Net Wt. 1 lb 1 oz (482 g),…

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

Schnucks Markets Corporate Office

FDA (openFDA food enforcement)

Food

Reported Aug 30, 2017

BUSH'S BEST¿ Brown Sugar Hickory SWEET HICKORY SAUCE WITH BROWN SUGAR & SPICES BAKED BEANS 28 OZ (1 LB 12 OZ) 794 g…

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

Bush Brothers & Co.

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 30, 2017

The Comfy Cow Banana Pudding Y'all Ice Cream 1 pint

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

Koogee-Queen Anne, LLC

8 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…

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

Medtronic Neuromodulation

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2017

Medium Coated Jo-Jo Wedges / 00040 (5lb bags)

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

Penobscot McCrum LLC

9 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2017

Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.

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

Shippert Medical Technologies

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VersaSafe Plastic Cannula - 11 Gauge, Model 9391-0200 Product Usage: Used with secondary IV sets or syringes with a…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…

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

Cyberonics, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner…

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

GE Medical Systems, LLC

8 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2017

Plum 360 Infusion System

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

ICU Medical Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 23, 2017

Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,

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

NatureAll-STF Holding, LLC

7 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 23, 2017

STUTZMAN FARMS Organic Spelt Berries 25 lb 11.4 kg 6197

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

Stutzman Farms

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 16, 2017

BARD DISPOZ-A-BAG Leg Bag with Flip-Flo Valve with Drain Extension, Extension Tube and Latex Straps, 19 oz. Packaged as…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body.…

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

International Medsurg Connection, Inc.

58 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 16, 2017

Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aortic Arch Cannulae are…

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

Sorin Group USA, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Aug 12, 2017

Luvo Inc. (USA) Recalls Poultry Products Due To Misbranding and Undeclared Allergens

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

Luvo Inc. (USA)

USDA FSIS

Food

Reported Aug 9, 2017

Professional Formulas Sublinqual B12 High-Potency dietary supplement, 60-count dissolvable tablet in white plastic…

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

Professional Complementary Health Formulas, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 9, 2017

InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the…

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

Quidel Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 2, 2017

North Atlantic Brand - Approx8OZ Raw Breaded Swai Fillet - NET WT. 10lbs (4.54KG)

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

Channel Fish Processing Co. Inc.

56 more products in this recall

FDA (openFDA food 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.

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.