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 Oct 1, 2014

The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)]…

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

Peters Surgical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 1, 2014

EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455

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

Vidacare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Ultraslim. These include all products labeled as UltraSlim, Luxurian, BioSlim Lipo, Cellulize, Slim 'n Trim, UltraRed,…

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

Advanced Photonic Systems, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Amerigel Wound Dressing Maximum Strength CAT# A2001. Wound management.

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

Amerx Health Care Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

BD BBL Vancomycin Screen Agar Catalog number 222204 Vancomycin Screen Agar is used to test enterococci for resistance…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResultNet is a stand-alone software package…

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

Data Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674,…

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

GF Health Products, Inc./d.b.a.Basic American Metal Products

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

TRx Vertical Positioner, Classification Name: Wheelchair Component - Power Positioning System.

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

Motion Concepts

FDA (openFDA device enforcement)

Medical devices

Reported Sep 24, 2014

AXIOM Luminos dRF system with SW VD10 or on Luminos dRF Max The Axiom Luminos dRF is intended to be used as a universal…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 24, 2014

Swanson 100% Certified Organic, Carob Powder, Raw Chocolate Substitute, Net wt 1 lb (454 grams), in round 1000 cc High…

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

Swanson Health Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2014

The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for the direct detection of…

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler…

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

Ethicon Endo-Surgery Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

CARESCAPE Respiratory Modules E-sCO, E-sCOV, E-sCAiO, E-sCAiOV, E-sCAiOE, E-sCAiOVE; the Airway Gas Option N-CAiO and…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2014

Stryker Aria Implant Inserter, REF 48758500, This instrument is part of the Aria product brand. It is used for Implant…

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

Stryker Spine

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Brown carob powder packed in a plastic heat sealed 16oz. bag, labeled in part "Live Superfoods Carob Powder***NET WT 16…

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

Live Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

EN MENTOR Round High Profile Single Use Saline Breast Implant Sizer Single Use Saline Breast Implant Sizer REF…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder; Certified Organic, Product of Italy. Store in Cool, Dark place. Packaged in 16 oz., 5 lb., 20 lb…

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

River Canyon Retreat

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

Roche cobas IT 1000 Product Usage: Intended Use: An electronic device intended to store, retrieve, and process…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2014

Organic Carob Powder, 1 lb., 20 lb., and 55 lb. bags Expiry date: 6/5/2015, UPC Code 803813-04429-8

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

Sunfood Superfoods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2014

PERSONA The Personalized Knee System Constrained Tibial Articular Surface Provisional BOTTOM with the following: L CD…

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

Zimmer, Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2014

Rising Moon Organics Butternut Squash Ravioli, Organic, Vegetarian & Delicious; Keep Frozen; Net Wt. 8 oz. UPC:…

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

Carmel Food Group, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2014

CloverSnare 4-Loop Vascular Retrieval Snare. Product is packaged in a Tyvek-film sterilizable outer package and is…

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

Cook Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2014

Cordis EMPIRA NC RX PTCA Dilatation Catheter

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

Cordis Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2014

ORGANIC TRADITIONS SPROUTED CHIA SEED POWDER NET WT. 8 oz. and 16 oz., UPC 854260006162, item number AHM616 and UPC…

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

Health Matters America Inc.

4 more products in this recall

FDA (openFDA food 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.