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 6, 2015

4.0mm Variable Angle, Self-Drilling Hexalobe Screw, 14mm Alphatec Spine Solutions for the Aging Spine Trestle Luxe…

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

Alphatec Spine, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2015

VNS Therapy DemiPulse Generator Model 103 and VNS Therapy DemiPulse Duo Generator Model 104; CYBERONICS, INC.

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

Cyberonics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2015

Test Request Distributor (TRD 1.3 and TRD 1.4), a software module used on the Dako Omnis System, an automated slide…

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

Dako North America Inc.

FDA (openFDA device enforcement)

Food

Reported May 6, 2015

JCB Flavors, LLC, Product Code 10064010, Chili Powder, 10 lb bulk.

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

JCB Flavors, LLC

41 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2015

Remote Network Station, Catalog RNS-9703, Model No. RNS-9703-19, RNS-9703-24, Software version 02.40. The RNS 9703 is…

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

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2015

Caviwave Pro Ultrasonic Cleaning System, Product Usage: To wash (remove tissue, blood and other contaminants) or dry…

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

Steris Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2015

Anatomical Shoulder Handle for Rasp Item: 01.04233.000 Used during total joint arthroplasty of the shoulder.

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

Zimmer GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2015

Captiva's lumbar intervertebral fusion system Reamers (color code rings on the Reamers).

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

Captiva Spine, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2015

The PCA 3 infusion pump allows clinicians, or patients, to (self) Administer analgesia safely and effectively within…

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

Hospira Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 29, 2015

La Guadalupana Salsa Verde Vegan Tamales are packed in a bulk plastic bag inside of a corrugated box and are stored…

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

La Guadalupana Wholesale Co. Inc.

FDA (openFDA food enforcement)

Drugs

Reported Apr 29, 2015

Droperidol injection, 2.5 mg/mL, 5 mg Total Dose, 2 mL Fill Volume per syringe, packaged in 10-count syringes per heat…

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

SCA Pharmaceuticals

FDA (openFDA drug enforcement)

Food

Reported Apr 29, 2015

Silver Lake Easter Egg Cookies, NET WT. 8 OZ (226g), UPC 0 37695 49817 1. Silver Lake Cookie Company, Inc. 141 Freeman…

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

Silver Lake Cookie Co., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2015

Master Drug Library Software version 8.0, Product Code 35723V080, to be used with SIGMA Spectrum Infusion System (Pump)…

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

Baxter Healthcare Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2015

WALLACH LL 100 cryosurgical units: LL100 Cryosurgical - Part Number 900001; LL110 with Pinned Yoke - Part Number…

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

CooperSurgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 22, 2015

Culinary Masters, SCHWARMA SPICE BLEND 1/50 LB, Shelf Life: 180 days.

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

Gourmet Foods International

32 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Apr 22, 2015

Twin Tree Gardens Premium Rubs "bunkhouse" Chicken Rub, Net Wt. 2.75 oz. (77g), Distributed by: Flavor Delight, Inc.,…

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

Haddon House Food Products Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 22, 2015

PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle

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

ReNew Life Formulas, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2015

Talon Grasping Device, 160 cm, US endoscopy. Used for retrieval of foreign bodies, tissue specimens, stones or calculi…

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

US Endoscopy Group Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

Instrument Kit for use with OsteoSponge SC grafts. The Instrument Kit is used to insert OsteoSponge SC grafts to fill…

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

Bacterin International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

CS 8100, CATALOG # (s): 5303045, 5311129, 5303060, 5303110 Intended to produce complete or segmented tomographic…

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

Carestream Health, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2015

Nutri-Dyn, 5-HTP Extra Strength, Pharmaceutical Grade from Switzerland, Dietary Supplement 60 capsules in plastic…

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

Nutri-Dyn Midwest, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2015

Pluer-evac Sahara Chest Drainage System, S-1100-08LF, Dry Suction/Dry Seal Control, Rx Only, Teleflex Medical.

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

Teleflex Medical

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2015

VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and…

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

VasoNova, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2015

Bard 100% Latex-Free Urinary Drainage Bag with Anti-Reflux Chamber and Bard EX-Lok Sampling; Product Code 154006: Lot #…

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

C.R. Bard, Inc.

FDA (openFDA device 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.