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 Nov 30, 2016

COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model…

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

AtriCure, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The…

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

DePuy Spine, Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

Organic Cacao Nibs, packaged in 200g (7.05 oz) brown bags, UPC code 661594002032

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

Level Ground Trading Limited

FDA (openFDA food enforcement)

Medical devices

Reported Nov 30, 2016

Merge RadSuite,f/k/a: Emageon Advanced Visualization , RadSuite versions 8.30.7.8, 8.30.7.9, 8.30.8, and 8.31. Advanced…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 30, 2016

Philips Healthcare System X-ray Tomography Computed :

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

Philips Electronics North America Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 30, 2016

Yoma Myanmar Tea Salad Snack - Spicy, 7 oz cello bag. Product of Myanmar

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

Yoma Myanmar

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

Access Ostase Calibrators, Catalog No. 37305, B83876 Product Usage: The Access Ostase Calibrators are intended to…

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

Beckman Coulter Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2016

Panera Bread Broccoli Cheddar Soup, 48 oz. sleeve (2/24 oz. cups/sleeve). Refrigerated UPC Code: 077958790918

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

Blount Fine Foods Corporation

FDA (openFDA food enforcement)

Food

Reported Nov 23, 2016

Simply Balanced brand White Chicken Chili dry soup mix. This is not a ready to eat product and it does not contain any…

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

Conifer Specialties, Inc.

FDA (openFDA food enforcement)

Food

Reported Nov 23, 2016

Frozen Onion Rings sold and distributed under the following private label retail brands: 1) Premium Pick 5 Mix and…

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

McCain Foods USA

FDA (openFDA food enforcement)

Medical devices

Reported Nov 23, 2016

Brilliance iCT Computed Tomography X-ray system, Model 728306

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

Philips Medical Systems (Cleveland) Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

Version 1.2.0 of Accu-Chek Connect Diabetes Management App (iOS) released on July 11, 2016

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

Roche Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 23, 2016

RF MultiGen¿, 0406-900-000; Refurb RF MultiGen¿, 0406-900-000U

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Food

Reported Nov 23, 2016

On Lid: Turkey Hill, Rocky Road, 48 FL. OZ.. In small letters at the top of the lid reads: "Dutch Chocolate ice cream…

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

Turkey Hill Dairy, LP

FDA (openFDA food enforcement)

Meat & poultry

Reported Nov 17, 2016

La Quercia Retira Productos De Cerdo Seco Por No Estar Suficientemente Deshidratados

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

La Quercia Operating LLC

USDA FSIS

Medical devices

Reported Nov 16, 2016

ReShape Integrated Dual Balloon System, Gen 1, Model No. 01-0013-001, Catalog No. RSM110 product Usage: The ReShape…

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

Reshape Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2016

The surgical table is a stand alone unit. Three (3) floor locking cylinders are attached to the base of the surgical…

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

Schaerer Medical USA Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 16, 2016

Zimmer¿ Air Dermatome II Handpiece Loaner, item number 01-8851-001-00. Device is packaged inside of a padded-foam…

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 12, 2016

Schnuck Markets Inc. Recalls Ready-To-Eat Chicken Breast Products That May Be Undercooked

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

Schnuck Markets, Inc. SLNP

USDA FSIS

Medical devices

Reported Nov 9, 2016

15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an…

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

Epimed International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2016

Xhibit Central Station, Model 96102. Intended use is to provide clinicians with central monitoring of adult, pediatric…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 9, 2016

Infusion Set, Comfort, 23" Hosp 10; Comfort 13mm, 23", STD 5/5; Comfort 13mm, 23" Hosp 10; Infusion Set, Comfort, 43",…

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

Unomedical As

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 2, 2016

SimpliRED D-Dimer, Product Code DSRK4 The SimpliRED D-dimer assay is a rapid, qualitative test for the detection of…

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

Bbi Solutions Oem Ltd.

FDA (openFDA device enforcement)

Food

Reported Nov 2, 2016

BRACH'S Chocolate Creations, Milk Chocolate Almond Supremes, Fresh roasted almonds drenched in rich creamy milk…

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

Ferrara Candy Comp

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.