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.

4,312 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.

Medical devices

Reported May 27, 2015

Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the…

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

Richard-Allan Scientific Company

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2015

Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2015

FujiMedical Synapse Cardiovascular I ProSolv CardioVascular. A picture Archiving and Communication System Software…

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

Fujifilm Medical Systems U.S.A., Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 20, 2015

Terra Spice Company Jalapeno Cheddar (dry spice mix). Sold in 0.5, 1, 3, or 5 qt. jars, 6x10 stand up pouches, and bulk…

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

Greenies LLC d.b.a. Terra Spice Company

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 20, 2015

Nuclear Gamma Cameras (ADAC Vertex Classic, ADAC VERTEX PLUS/SOLUS/CARDIO, ADAC VERTEX V60) Philips Medical Systems,…

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

Philips Medical Systems (Cleveland) Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2015

Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component of the Mercury Spinal System, comprised of a variety of…

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

Spinal Elements, Inc.

FDA (openFDA device enforcement)

Food

Reported May 20, 2015

Tastefully Simple, Blackberry Syrup, 12 FL oz ( 360 ml), Item 763905. Ingredients: Corn syrup, blackberries, cane…

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

Tastefully Simple, Inc.

FDA (openFDA food enforcement)

Food

Reported May 20, 2015

Trader Joe's Nuts Raw California Walnut Pieces NET WT. 16oz. (1 LB) 454g UPC 00373685 Trader Joe's Nuts Raw California…

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

Trader Joes Company

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2015

BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g x 20cm The BARD MAX-CORE Disposable Core Biopsy…

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

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2015

EOS, Digital radiography system used in general radiographic examinations.

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

Eos Imaging Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2015

NexGen Augment; 5mm Distal Femoral Augment;Part number 00-5990-036-10. Intended to be used in total knee arthroplasty…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

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)

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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.