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 48,828 notices were distributed nationwide, so they reach Indiana too — those are in the archive.

Medical devices

Reported Jul 27, 2016

DeVilbiss Model 7305P-D Powered Suction Unit

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

DeVilbiss Healthcare LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

ATEC CANISTER. Suction Canister with Lid 490 cc., RX Only; Suction canister used to collect fluid during a breast…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Kellogg's Special K Mini Brownies Blondie, 6 ct, 4.44 oz.

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

Kellogg Company

24 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jul 27, 2016

Navitas Naturals Superfood Hemp bar: Creamy Peanut, Hemp, Nut Bar. Net Wt. 1.4 oz/40 G. Gluten free. Ingredients:…

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

Navitas, LLC.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

Syngo.via, picture archiving and communications system software controlled. Intended to be used for viewing,…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 27, 2016

Tosi Cappuccino Crunch Almond SuperBites, 12 bars per pack, Net Wt. 2.6 ounces, UPC 755918046106

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

Simple Health LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 27, 2016

OT1000 Series Orthopedic Surgical Tables

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

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

Depuy Synthes Trauma- Trochanteric Fixation Nail Advanced (TFNA) Blade/Screw Guide Sleeve, Surgical Instrument Part…

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 27, 2016

HX2" Temperature Management Systems; The Terumo¿ HX2" Temperature Management System provides temperature control of two…

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

Terumo Cardiovascular Systems Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

HeartWare Ventricular Assist System: HeartWare Battery, Lithium Ion, 14.8 V, Rx only. Catalog 1650 (US) and 1650,…

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

Heartware, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

The LifeCare PCA Plus II infusion pump system is designed for safe, effective, analgesic delivery to patients through…

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

Hospira Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 20, 2016

6.5 mm Cannulated Screw, Product code HWC, Device Listing Number D028949, Screw, Fixation Bone Product Usage: Intended…

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

Synthes (USA) Products LLC

17 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jul 20, 2016

Kroger SALAD TOPPERS Roasted & Salted Sunflower Kernels NET WT 3.5 OZ (99G) INGREDIENTS: SUNFLOWER KERNELS, COTTONSEED…

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

The Kroger Co.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 13, 2016

The System 83 Plus, Endoscope Washer/Disinfector Designed for the simultaneous reprocessing of up to two flexible…

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

Custom Ultrasonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2016

GE Healthcare, Discovery MR750w

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 13, 2016

Synthes Ti Button Plate 7 Holes, Fastener, Fixation, nondegradable, Soft Tissue

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

Synthes (USA) Products LLC

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

PrismaSate BGK2/0 Dialysis Solution for Continuous Renal Replacement Therapy

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

Bigger-Better-Bladder With 3/8" ID tubing, ITEM BBB38

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

Circulatory Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

IMPAK Liquid Acrylic Resin sold under the following labels: 1) IMPAK PF PINK-FIBERED ELASTIC ACRYLIC RESIN LIQUID, 11…

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

CMP Industries, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

MOSAIQ Oncology Information System

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 6, 2016

Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital, Finger Catalog…

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

Medtronic Sofamor Danek USA, Inc. - Dallas Distribution

FDA (openFDA device enforcement)

Food

Reported Jul 6, 2016

Productos Del Campo Castillo Chile Habanero (Fresh Habanero Peppers)

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

Montero Farms

FDA (openFDA food enforcement)

Food

Reported Jul 6, 2016

Reser's Deviled Egg Potato Salad, Refrigerated, Retail package, Net wt. 3 lbs. UPC 0 71117 00480 9; Reser's Deviled Egg…

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

Reser's Fine Foods, Inc. - Century

7 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 6, 2016

Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module…

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

Siemens Healthcare Diagnostics Inc.

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.