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.

4,310 stored notices name Indiana, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,842 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Food

Reported Mar 23, 2016

Citrus Flavored Soda Mello Yello, 12 fl. oz. (355 ml), Canned under authority of The Coca-Cola Company, Atlanta, GA…

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

Coca-Cola Company (The)

FDA (openFDA food enforcement)

Medical devices

Reported Mar 23, 2016

CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…

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

Cordis Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic…

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

Deerfield Imaging

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 23, 2016

Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…

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

Arrow International Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of…

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

Bard Peripheral Vascular Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Mar 16, 2016

Tofu Curry Cous Cous Salad packaged in a clear plastic 16 oz box with a white and green label with black lettering.

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

Brett Anthony Foods

FDA (openFDA food enforcement)

Food

Reported Mar 16, 2016

Bertolli Extra Virgin Olive Oil, 8.5 oz. and Carapelli Extra Virgin Olive Oil, 25.5 oz., packaged in glass bottles.

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

DEOLEO USA, Inc.

FDA (openFDA food enforcement)

Food

Reported Mar 16, 2016

ORGANIC HOMESTAT FARM Quick STEEL CUT OATS & CHIA with Flax and Rye Flakes NET WT 42 OZ (2 LB. 10 OZ.)…

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

Homestat Farm Ltd.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 16, 2016

TF Adaptive Gutta Percha Point Size SM3 50pk, Part No. 815-1541 Intended to fill a endontontically obturated root canal…

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

Ormco/Sybronendo

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10 is intended…

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

Philips Electronics North America Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Mobile wDR motorized portable diagnostic X-ray systems. Intended for use by a qualified/trained doctor or technologist…

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

Sedecal S.A.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog Number: 04634452 SMN: 10309079 ADVIA…

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

Siemens Healthcare Diagnostics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

Spacelabs Healthcare Xhibit Central Station, Model 96102 is used to provide clinicians with central monitoring of…

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

Spacelabs Healthcare Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 16, 2016

ROTROL P Control for ROTEM delta Thromboelastometry System, For In Vitro Diagnostic Use Only. Quality control material…

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

TEM Systems Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 9, 2016

Braga Organic Farms Organic Pistachio Kernels, Raw; Certified Organic, USDA Organic. Packed in 8 oz. 1 lb. 2. lb and 5…

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

Braga Organic Farms, Inc.

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 9, 2016

Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended to spray liquids in aerosol form into gasses…

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

ConvaTec, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

Helioseal Clear Refill 1 x 1.25 g, REF/Product Code/Art. No. 558521AN and Helioseal Clear Assortment 5 x 1.25 g,…

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

Ivoclar Vivadent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 9, 2016

BrightView are gamma cameras; Designed for single or dual detector nuclear imaging.

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

Philips Medical Systems (Cleveland) Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Mar 5, 2016

Perdue Foods LLC, Retira Productos De Trozos De Pollo Empanado Por Posible Contaminacin Con Material Extrao

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

Gold Creek Foods, LLC

USDA FSIS

Medical devices

Reported Mar 2, 2016

Hill-Rom Bariatric Power Recliner, Product Model # P9096 Hill-Roms 660 lb Powered Bariatric Recliner was created to…

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

Hill-Rom, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 2, 2016

Purple Cow Limited Edition Cookie Butter Ice Cream, 8 oz. cups, packed in paper cartons

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

House Of Flavors, 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.