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 Aug 13, 2014

Sonopet Ultrasonic Surgical System Console, Ultrasonic Aspirator, Stryker Medtech.

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

Stryker Instruments Div.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

DeRoyal KNEE ARTHROSCOPY PACK, REF 89-6192.04, 1 Per Pack, Distributed by: DeRoyal Industries, Inc.; Manufacturer:…

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

DeRoyal Industries Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Horizon Medical Imaging It is a medical image and information management application that is intended to receive,…

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

Mckesson Medical Immaging

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw System Sets, Implants, and Instruments…

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

Small Bone Innovations

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2014

InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.

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

Stryker Medical Division

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

AGFA Digital Radiography X-Ray system DX-D 100 Agfa's DX-D 100 is indicated for use in providing diagnostic quality…

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

AGFA Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

RECLAIM Taper Protector Sleeve. RECLAIM Revision Hip System Orthopedic Manual Surgical Instrument, used to ensure the…

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

DePuy Orthopaedics, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2014

MK5 NX Controller--Wheelchair controller

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

Invacare Corporation

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2014

Fat free cottage cheese sold under the Knudsen or Kraft brand and packaged in a plastic container with a net weight of…

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

Kraft Foods Group

10 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 30, 2014

Item: 4815 Land O'Lakes, Extra Melt American White, Pasteurized Process American Cheese, Net WT 5 lbs (2.26 KG)

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

Land O' Lakes, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2014

Sarns D4 Aortic Arch Cannulae 6.0mm, 7mm & 8mm angled and straight tip with or without side holes and/or luer Product…

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

Terumo Cardiovascular Systems Corporation

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

Titan T 5K Motor Product Usage: Low-speed motor is used with various attachments to perform a variety of dental…

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

Dental EZ Group Star Dental Division

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2014

ACL TOP (Base), automated coagulation laboratory instrument.

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

Instrumentation Laboratory Co.

6 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Velveeta Original Pasteurized Ripe Cheese Product sold under the Kraft brand and individually wrapped in plastic and…

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

Kraft Foods Group

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

LP,Surgical Fibers, Bare Laser Fiber 600 micron, DBLF-60-2, Sterile EO. Laser surgical instrument for use in general…

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

Laser Peripherals LLC

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

There are 2 different labels for this same product with the same UPC. Label #1 Individual Bars: 100% natural Zing…

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

NW Nutritional Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

Thermo Scientific VersaTREK REDOX 1, Ref 7102-44, 80ml with Stir Bar (O2 aerobic), 50 bottles/box, IVD. The firm name…

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

Remel Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2014

Schnucks Bakery 8" Devil's Food Cake, net wt. 2 lb 13 oz, UPC: 04131831186. Also packaged as Schnucks Bakery Half…

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

Schnucks Markets Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 23, 2014

e.cam camera system. Emission Computed Tomography System used to detect or image the distribution of radionuclides in…

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

Siemens Medical Solutions USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Devon Supine, Lithotomy and Trendelenburg Positioning Kit; Product Code: 31151090 Product Usage: The device is intended…

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

Covidien LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 16, 2014

Essential NEO, Audio/Visual Integration Unit An audio/visual integration unit.

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Food

Reported Jul 16, 2014

Chocolate Ice Cream, Manufactured by: Koogee-Queen Anne, LLC, d/b/a The Comfy Cow 2221 Frankfort Ave, Louisville, KY…

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

Koogee-Queen Anne, LLC

77 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 16, 2014

Mountain House Freeze-Dried Precooked Scrambled Eggs with Ham and Red & Green Peppers, 19.4 oz 1 LB 3.4 oz), packed in…

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

Oregon Freeze Dry, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Jul 16, 2014

PALL Medical Breathing Circuit Filter, REF BB50T and BB50T-BULK , Rx ONLY Single use, bi-directional bacterial/viral…

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

Pall Corporation

FDA (openFDA device 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.