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 May 9, 2018

StoneBreaker Pneumatic Lithotripter, Catalog number: SBL-KIT1; GPN: G52604 UDI:(01)00827002526044

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

Cook Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 9, 2018

5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage:…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 9, 2018

Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for…

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

IntroMedic Co., Ltd.

FDA (openFDA device enforcement)

Food

Reported May 9, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc.…

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

Mccall Farms Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 9, 2018

Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray…

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 May 9, 2018

Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented…

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

clariti 1 day/Fresh Day 90 pack (-1.00), UV Blocking, 90 silicon hydrogel, daily disposable contact lenses The Clariti…

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

CooperVision Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM, Product Number HEM3335, GTIN Number 1 -…

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

Covidien LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 2, 2018

Versatex Monofilament Mesh 50 x 50cm, Product No. VTX5050M The device is made out of a macroporous three-dimensional…

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

Sofradim Production

FDA (openFDA device enforcement)

Meat & poultry

Reported May 2, 2018

JBS USA, Inc. Recalls Ground Beef Products Due to Possible Foreign Matter Contamination

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

Swift Beef Company

USDA FSIS

Food

Reported Apr 25, 2018

Kratom capsules labeled in the following ways: 1) Divinity Kratom 10 Capsule Dietary Supplement, Divinity Product LLC,…

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

Divinity Product Distribution LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Human Fetal Hemoglobin (HBF-1) FITC Conjugate

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

Life Technologies Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

Midwest Northern Nut Roasted Salted Natural Almonds. Packaged in the following sizes: 1. Net Wt. 16 oz. (454G), UPC…

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

Midwest Northern Inc.

65 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

MEVATRON M2 / PRIMUS Mid-Energy, Digital Linear Accelerator, Model No. 01940035 Product Usage: The intended use of the…

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

Siemens Medical Solutions USA, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 25, 2018

SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8

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

Smucker Natural Foods, Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 25, 2018

HUNGRY JACK Original PANCAKE & WAFFLE MIX NET WT 32 OZ (2 LB) 907 g

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

The J.M. Smucker Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 25, 2018

Zimmer Segmental System Proximal Femoral Component 38mm Offset, Model Number 00-5850-030-38 The Segmental System is…

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

Zimmer Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and…

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

Hamilton Medical AG

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

AUTO REF/KERATOMETER ARK-1s

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

Nidek Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 18, 2018

Normed Charcot Osteotome Chisel (Various sizes)

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

Zimmer GmbH

FDA (openFDA device enforcement)

Meat & poultry

Reported Apr 14, 2018

Fresh Foods Manufacturing Co. Recalls Ready-To-Eat Salad Products Due to Possible E. coli O157:H7 Contamination

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

Fresh Food Manufacturing Company

USDA FSIS

Medical devices

Reported Apr 11, 2018

Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number…

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

Phadia Ab

FDA (openFDA device enforcement)

Medical devices

Reported Apr 11, 2018

Elecsys BRAHMS PCT Immunoassay for the in vitro quantitative determination of PCT (procalcitonin) in human serum and…

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

Roche Diagnostics Corporation

FDA (openFDA device enforcement)

Food

Reported Apr 11, 2018

King Arthur Flour, 100% Organic, Finely Ground, Coconut Flour, UPC 0 71012 10702 5, Distributed by: The King Arthur…

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

The King Arthur Flour Company, Inc.

FDA (openFDA food enforcement)

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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.